All Stories

  1. Modulation of α-synuclein in vitro aggregation kinetics by its alternative splice isoforms
  2. Multiomic prediction of therapeutic targets for human diseases associated with protein phase separation
  3. Formation of amyloid loops in brain tissues is controlled by the flexibility of protofibril chains
  4. Spontaneous nucleation and fast aggregate-dependent proliferation of α-synuclein aggregates within liquid condensates at neutral pH
  5. Widespread occurrence of the droplet state of proteins in the human proteome
  6. Rational design of a conformation-specific antibody for the quantification of Aβ oligomers
  7. Sequence-based prediction of protein binding mode landscapes
  8. Chris Dobson (1949–2019)
  9. Widespread remodeling of proteome solubility in response to different protein homeostasis stresses
  10. The N-terminal Acetylation of α-Synuclein Changes the Affinity for Lipid Membranes but not the Structural Properties of the Bound State
  11. Dynamics of oligomer populations formed during the aggregation of Alzheimer’s Aβ42 peptide
  12. Proteome-wide observation of the phenomenon of life on the edge of solubility
  13. Determination of a Structural Ensemble Representing the Dynamics of a G-Quadruplex DNA
  14. Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons
  15. Bacterial production and direct functional screening of expanded molecular libraries for discovering inhibitors of protein aggregation
  16. Probing the dynamic stalk region of the ribosome using solution NMR
  17. Differential Interactome and Innate Immune Response Activation of Two Structurally Distinct Misfolded Protein Oligomers
  18. Determination of protein structural ensembles using cryo-electron microscopy
  19. Expression of the amyloid-β peptide in a single pair of C. elegans sensory neurons modulates the associated behavioural response
  20. Probing the Origin of the Toxicity of Oligomeric Aggregates of α-Synuclein with Antibodies
  21. Identifying A- and P-site locations on ribosome-protected mRNA fragments using Integer Programming
  22. The free energy landscape of the oncogene protein E7 of human papillomavirus type 16 reveals a complex interplay between ordered and disordered regions
  23. Secondary nucleation and elongation occur at different sites on Alzheimer’s amyloid-β aggregates
  24. A method of predicting the in vitro fibril formation propensity of Aβ40 mutants based on their inclusion body levels in E. coli
  25. Atomic force microscopy for single molecule characterisation of protein aggregation
  26. A superposition free method for protein conformational ensemble analyses and local clustering based on a differential geometry representation of backbone
  27. Trodusquemine enhances Aβ42 aggregation but suppresses its toxicity by displacing oligomers from cell membranes
  28. Effects of α-tubulin acetylation on microtubule structure and stability
  29. Chemical and mechanistic analysis of photodynamic inhibition of Alzheimer's β-amyloid aggregation
  30. Bayesian Weighing of Electron Cryo-Microscopy Data for Integrative Structural Modeling
  31. A tau homeostasis signature is linked with the cellular and regional vulnerability of excitatory neurons to tau pathology
  32. Identifying A- and P-site locations on ribosome-protected mRNA fragments using Integer Programming
  33. In vitro and in silico assessment of the developability of a designed monoclonal antibody library
  34. Determination of Structural Ensembles of Proteins: Restraining vs Reweighting
  35. Automated Behavioral Analysis of Large C. elegans Populations Using a Wide Field-of-view Tracking Platform
  36. SAR by kinetics for drug discovery in protein misfolding diseases
  37. Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity
  38. Intrinsically aggregation-prone proteins form amyloid-like aggregates and contribute to tissue aging in C. elegans
  39. Fast fluorescence lifetime imaging reveals the aggregation processes of α-synuclein and polyglutamine in aging Caenorhabditis elegans
  40. Systematic mapping of free energy landscapes of a growing filamin domain during biosynthesis
  41. Stabilization and Characterization of Cytotoxic Aβ40 Oligomers Isolated from an Aggregation Reaction in the Presence of Zinc Ions
  42. Author Correction: The molecular chaperones DNAJB6 and Hsp70 cooperate to suppress α-synuclein aggregation
  43. Structural Ensemble Modulation upon Small-Molecule Binding to Disordered Proteins
  44. Massively parallel C. elegans tracking provides multi-dimensional fingerprints for phenotypic discovery
  45. Molecular dynamics ensemble refinement of the heterogeneous native state of NCBD using chemical shifts and NOEs
  46. Determination of the conformational states of strychnine using NMR residual dipolar couplings in a tensor-free approach
  47. Exploring the role of post-translational modifications in regulating α-synuclein interactions by studying the effects of phosphorylation on nanobody binding
  48. Multistep Inhibition of α-Synuclein Aggregation and Toxicity in Vitro and in Vivo by Trodusquemine
  49. Reversible inhibition of the ClpP protease via an N-terminal conformational switch
  50. Cooperative Assembly of Hsp70 Subdomain Clusters
  51. A method for partitioning the information contained in a protein sequence between its structure and function
  52. A Rationally Designed Hsp70 Variant Rescues the Aggregation-Associated Toxicity of Human IAPP in Cultured Pancreatic Islet β-Cells
  53. Developing NMR methods for macromolecular machines: Measurement of residual dipolar couplings to probe dynamical regions of the ribosome
  54. Cholesterol catalyses Aβ42 aggregation through a heterogeneous nucleation pathway in the presence of lipid membranes
  55. Chemical Kinetics for Bridging Molecular Mechanisms and Macroscopic Measurements of Amyloid Fibril Formation
  56. Parapred: antibody paratope prediction using convolutional and recurrent neural networks
  57. FUS Phase Separation Is Modulated by a Molecular Chaperone and Methylation of Arginine Cation-π Interactions
  58. Simultaneous Determination of Protein Structure and Dynamics Using Cryo-Electron Microscopy
  59. Molecular determinants of the interaction of EGCG with ordered and disordered proteins
  60. Distinct thermodynamic signatures of oligomer generation in the aggregation of the amyloid-β peptide
  61. Molecular dynamics ensemble refinement of the heterogeneous native state of NCBD using chemical shifts and NOEs
  62. Third generation antibody discovery methods:in silicorational design
  63. Structural differences between toxic and nontoxic HypF-N oligomers
  64. Structural basis of membrane disruption and cellular toxicity by α-synuclein oligomers
  65. Simultaneous Determination of Protein Structure and Dynamics Using Cryo-Electron Microscopy
  66. MobiDB 3.0: more annotations for intrinsic disorder, conformational diversity and interactions in proteins
  67. Delivery of Native Proteins into C. elegans Using a Transduction Protocol Based on Lipid Vesicles
  68. Oxetane Grafts Installed Site-Selectively on Native Disulfides to Enhance Protein Stability and Activity In Vivo
  69. In Vitro and In Silico Activity of Iridoids Against Leishmania ama-zonensis
  70. Influence of Harvest Season and Cultivar on the Variation of Phenolic Compounds Composition and Antioxidant Properties in Vaccinium ashei Leaves
  71. Systematic mapping of the free energy landscapes of a growing immunoglobulin domain identifies a kinetic intermediate associated with co-translational proline isomerization
  72. Paratope Prediction using Convolutional and Recurrent Neural Networks
  73. Sequence Specificity in the Entropy-Driven Binding of a Small Molecule and a Disordered Peptide
  74. The molecular chaperones DNAJB6 and Hsp70 cooperate to suppress α-synuclein aggregation
  75. Rapid and accurate in silico solubility screening of a monoclonal antibody library
  76. Monomeric and fibrillar α-synuclein exert opposite effects on the catalytic cycle that promotes the proliferation of Aβ42 aggregates
  77. Nanobodies raised against monomeric ɑ-synuclein inhibit fibril formation and destabilize toxic oligomeric species
  78. Protein homeostasis of a metastable subproteome associated with Alzheimer’s disease
  79. Methods of probing the interactions between small molecules and disordered proteins
  80. Amyloid-like Fibrils from an α-Helical Transmembrane Protein
  81. Phage display and kinetic selection of antibodies that specifically inhibit amyloid self-replication
  82. Selective targeting of primary and secondary nucleation pathways in Aβ42 aggregation using a rational antibody scanning method
  83. Corrigendum: Structural basis of synaptic vesicle assembly promoted by α-synuclein
  84. Structural Characterization of the Early Events in the Nucleation–Condensation Mechanism in a Protein Folding Process
  85. The RNF168 paralog RNF169 defines a new class of ubiquitylated histone reader involved in the response to DNA damage
  86. Emergence and evolution of an interaction between intrinsically disordered proteins
  87. Spinal motor neuron protein supersaturation patterns are associated with inclusion body formation in ALS
  88. MOAG-4 promotes the aggregation of α-synuclein by competing with self-protective electrostatic interactions
  89. Simultaneous quantification of protein order and disorder
  90. Bayesian weighing of electron cryo-microscopy data for integrative structural modeling
  91. Identification of an RNA Polymerase III Regulator Linked to Disease-Associated Protein Aggregation
  92. Inhibition of α-Synuclein Fibril Elongation by Hsp70 Is Governed by a Kinetic Binding Competition between α-Synuclein Species
  93. Widespread Proteome Remodeling and Aggregation in Aging C. elegans
  94. Networks of Dynamic Allostery Regulate Enzyme Function
  95. Principles of protein structural ensemble determination
  96. A natural product inhibits the initiation of α-synuclein aggregation and suppresses its toxicity
  97. Scaling behaviour and rate-determining steps in filamentous self-assembly
  98. Simultaneous NMR characterisation of multiple minima in the free energy landscape of an RNA UUCG tetraloop
  99. Systematic development of small molecules to inhibit specific microscopic steps of Aβ42 aggregation in Alzheimer’s disease
  100. β-Synuclein suppresses both the initiation and amplification steps of α-synuclein aggregation via competitive binding to surfaces
  101. Simultaneous Production of Amyloglucosidase and Exo-Polygalacturonase by Aspergillus niger in a Rotating Drum Reactor
  102. Structural basis of synaptic vesicle assembly promoted by α-synuclein
  103. Mutations associated with familial Parkinson’s disease alter the initiation and amplification steps of α-synuclein aggregation
  104. Metadynamic metainference: Enhanced sampling of the metainference ensemble using metadynamics
  105. A protein homeostasis signature in healthy brains recapitulates tissue vulnerability to Alzheimers disease
  106. Towards a structural biology of the hydrophobic effect in protein folding
  107. Chemical properties of lipids strongly affect the kinetics of the membrane-induced aggregation of α-synuclein
  108. Structure of a low-population binding intermediate in protein-RNA recognition
  109. Structural Ensembles of Membrane-bound α-Synuclein Reveal the Molecular Determinants of Synaptic Vesicle Affinity
  110. Structural Effects of Two Camelid Nanobodies Directed to Distinct C-Terminal Epitopes on α-Synuclein
  111. Rational design of mutations that change the aggregation rate of a protein while maintaining its native structure and stability
  112. Structural characterization of the interaction of α-synuclein nascent chains with the ribosomal surface and trigger factor
  113. A transcriptional signature of Alzheimer’s disease is associated with a metastable subproteome at risk for aggregation
  114. Kinetic analysis reveals the diversity of microscopic mechanisms through which molecular chaperones suppress amyloid formation
  115. Identification and Structural Characterization of an Intermediate in the Folding of the Measles Virus X Domain
  116. A structural ensemble of a ribosome–nascent chain complex during cotranslational protein folding
  117. A Fragment-Based Method of Creating Small-Molecule Libraries to Target the Aggregation of Intrinsically Disordered Proteins
  118. Molecular Recognition by Templated Folding of an Intrinsically Disordered Protein
  119. An anticancer drug suppresses the primary nucleation reaction that initiates the production of the toxic A 42 aggregates linked with Alzheimers disease
  120. Microfluidic Diffusion Analysis of the Sizes and Interactions of Proteins under Native Solution Conditions
  121. Metainference: A Bayesian inference method for heterogeneous systems
  122. Hamiltonian Dynamics of Protein Filament Formation
  123. Molecular mechanisms of protein aggregation from global fitting of kinetic models
  124. Particle-Based Monte-Carlo Simulations of Steady-State Mass Transport at Intermediate Péclet Numbers
  125. Structural Insights into the Calcium-Mediated Allosteric Transition in the C-Terminal Domain of Calmodulin from Nuclear Magnetic Resonance Measurements
  126. Using Pseudocontact Shifts and Residual Dipolar Couplings as Exact NMR Restraints for the Determination of Protein Structural Ensembles
  127. Parmbsc1: a refined force field for DNA simulations
  128. Structure-Free Validation of Residual Dipolar Coupling and Paramagnetic Relaxation Enhancement Measurements of Disordered Proteins
  129. ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function
  130. Mapping the Protein Fold Universe Using the CamTube Force Field in Molecular Dynamics Simulations
  131. The inverted free energy landscape of an intrinsically disordered peptide by simulations and experiments
  132. Identification of Small Molecule Inhibitors of Tau Aggregation by Targeting Monomeric Tau As a Potential Therapeutic Approach for Tauopathies
  133. Latent analysis of unmodified biomolecules and their complexes in solution with attomole detection sensitivity
  134. Targeting disordered proteins with small molecules using entropy
  135. Chromatin Unfolding by Epigenetic Modifications Explained by Dramatic Impairment of Internucleosome Interactions: A Multiscale Computational Study
  136. A Rational Design Strategy for the Selective Activity Enhancement of a Molecular Chaperone toward a Target Substrate
  137. Rational design of antibodies targeting specific epitopes within intrinsically disordered proteins
  138. Probing the Residual Structure of the Low Populated Denatured State of ADA2h under Folding Conditions by Relaxation Dispersion Nuclear Magnetic Resonance Spectroscopy
  139. Reply to “Comment on ‘A Tensor-Free Method for the Structural and Dynamic Refinement of Proteins using Residual Dipolar Couplings’”
  140. Dynamic binding mode of a Synaptotagmin-1–SNARE complex in solution
  141. Analysis of the performance of the CHESHIRE and YAPP methods at CASD-NMR round 3
  142. Structure and Dynamics of GeoCyp: A Thermophilic Cyclophilin with a Novel Substrate Binding Mechanism That Functions Efficiently at Low Temperatures
  143. Widespread Proteome Remodeling and Aggregation in Aging C. elegans
  144. Structure and Dynamics of the Integrin LFA-1 I-Domain in the Inactive State Underlie its Inside-Out/Outside-In Signaling and Allosteric Mechanisms
  145. The physical basis of protein misfolding disorders
  146. A molecular chaperone breaks the catalytic cycle that generates toxic Aβ oligomers
  147. Lipid vesicles trigger α-synuclein aggregation by stimulating primary nucleation
  148. The s2D Method: Simultaneous Sequence-Based Prediction of the Statistical Populations of Ordered and Disordered Regions in Proteins
  149. Supersaturation is a major driving force for protein aggregation in neurodegenerative diseases
  150. A Tensor-Free Method for the Structural and Dynamical Refinement of Proteins using Residual Dipolar Couplings
  151. Structure of a low-population intermediate state in the release of an enzyme product
  152. The CamSol Method of Rational Design of Protein Mutants with Enhanced Solubility
  153. Analysis of the hierarchical structure of the B. subtilis transcriptional regulatory network
  154. The Computational Studies of Co-Translational Protein Folding
  155. Biophysical approaches for the study of interactions between molecular chaperones and protein aggregates
  156. Druggability of Intrinsically Disordered Proteins
  157. Structure and Dynamics of Intrinsically Disordered Proteins
  158. The H50Q Mutation Induces a 10-fold Decrease in the Solubility of α-Synuclein
  159. Characterization of the Conformational Fluctuations in the Josephin Domain of Ataxin-3
  160. A Relationship between the Transient Structure in the Monomeric State and the Aggregation Propensities of α-Synuclein and β-Synuclein
  161. ADP ribosylation adapts an ER chaperone response to short-term fluctuations in unfolded protein load
  162. Understanding the frustration arising from the competition between function, misfolding, and aggregation in a globular protein
  163. Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein
  164. NMR characterization of the conformational fluctuations of the human lymphocyte function‐associated antigen‐1 I‐domain
  165. Equilibrium simulations of proteins using molecular fragment replacement and NMR chemical shifts
  166. Archaeal MBF1 binds to 30S and 70S ribosomes via its helix–turn–helix domain
  167. Cyclophilin A catalyzes proline isomerization by an electrostatic handle mechanism
  168. Statistical Mechanics of the Denatured State of a Protein Using Replica-Averaged Metadynamics
  169. A tensor-free method for the structural and dynamical refinement of proteins using residual dipolar couplings
  170. Flexible anchoring of archaeal MBF1 on ribosomes suggests role as recruitment factor
  171. Erratum: The amyloid state and its association with protein misfolding diseases
  172. Direct observation of the three regions in α-synuclein that determine its membrane-bound behaviour
  173. The amyloid state and its association with protein misfolding diseases
  174. Understanding the Influence of Codon Translation Rates on Cotranslational Protein Folding
  175. Solution conditions determine the relative importance of nucleation and growth processes in α-synuclein aggregation
  176. Determination of the Individual Roles of the Linker Residues in the Interdomain Motions of Calmodulin Using NMR Chemical Shifts
  177. ALMOST: An all atom molecular simulation toolkit for protein structure determination
  178. Spatial Propagation of Protein Polymerization
  179. Chemical kinetics for drug discovery to combat protein aggregation diseases
  180. Targeting the Intrinsically Disordered Structural Ensemble of α-Synuclein by Small Molecules as a Potential Therapeutic Strategy for Parkinson’s Disease
  181. The dynamics of interleukin‐8 and its interaction with human CXC receptor I peptide
  182. A Conformational Ensemble Derived Using NMR Methyl Chemical Shifts Reveals a Mechanical Clamping Transition That Gates the Binding of the HU Protein to DNA
  183. New opportunities for tensor-free calculations of residual dipolar couplings for the study of protein dynamics
  184. A Simple Lattice Model That Captures Protein Folding, Aggregation and Amyloid Formation
  185. Kinetic modelling indicates that fast-translating codons can coordinate cotranslational protein folding by avoiding misfolded intermediates
  186. Structure of a Misfolded Intermediate of a PDZ Domain
  187. Higher Order Amyloid Fibril Structure by MAS NMR and DNP Spectroscopy
  188. A Clear View of Polymorphism, Twist, and Chirality in Amyloid Fibril Formation
  189. Replica-Averaged Metadynamics
  190. Widespread Aggregation and Neurodegenerative Diseases Are Associated with Supersaturated Proteins
  191. pE-DB: a database of structural ensembles of intrinsically disordered and of unfolded proteins
  192. Erratum: “Molecular dynamics simulations with replica-averaged structural restraints generate structural ensembles according to the maximum entropy principle” [J. Chem. Phys. 138, 094112 (2013)]
  193. Subdomain Architecture and Stability of a Giant Repeat Protein
  194. Cucurbit[8]uril and Blue-Box: High-Energy Water Release Overwhelms Electrostatic Interactions
  195. A Relationship between the Aggregation Rates of α-Synuclein Variants and the β-Sheet Populations in Their Monomeric Forms
  196. Characterization of the Interdomain Motions in Hen Lysozyme Using Residual Dipolar Couplings as Replica-Averaged Structural Restraints in Molecular Dynamics Simulations
  197. Structures of the Excited States of Phospholamban and Shifts in Their Populations upon Phosphorylation
  198. In-Cell NMR Characterization of the Secondary Structure Populations of a Disordered Conformation of α-Synuclein within E. coli Cells
  199. A geometrical parametrization of C1′-C5′ RNA ribose chemical shifts calculated by density functional theory
  200. Identification of small-molecule binding pockets in the soluble monomeric form of the Aβ42 peptide
  201. Nanobodies Raised against Monomeric α-Synuclein Distinguish between Fibrils at Different Maturation Stages
  202. Single-Molecule Measurements of Transient Biomolecular Complexes through Microfluidic Dilution
  203. A method of determining RNA conformational ensembles using structure-based calculations of residual dipolar couplings
  204. Proliferation of amyloid-β42 aggregates occurs through a secondary nucleation mechanism
  205. Integration and characterization of solid wall electrodes in microfluidic devices fabricated in a single photolithography step
  206. The codon information index: a quantitative measure of the information provided by the codon bias
  207. Characterization of the free-energy landscapes of proteins by NMR-guided metadynamics
  208. Atomic structure and hierarchical assembly of a cross-β amyloid fibril
  209. Protein self-assembly intermediates
  210. Molecular dynamics simulations with replica-averaged structural restraints generate structural ensembles according to the maximum entropy principle
  211. Erratum: Prediction of variable translation rate effects on cotranslational protein folding
  212. Analysis of the Contributions of Ring Current and Electric Field Effects to the Chemical Shifts of RNA Bases
  213. Assessment of the Use of NMR Chemical Shifts as Replica-Averaged Structural Restraints in Molecular Dynamics Simulations to Characterize the Dynamics of Proteins
  214. R state structure of monomeric phospholamban (C36A, C41F, C46A)
  215. Sequence-Based Prediction of Protein Behavior
  216. The Kinetics and Mechanisms of Amyloid Formation
  217. Characterization of Free Energy Landscapes of Proteins using NMR Spectroscopy
  218. In Vivo Translation Rates Can Substantially Delay the Co-Translational Folding of the E. Coli Cytosolic Proteome
  219. Thermodynamics of an Intrinsically Disordered Protein by Atomistic Simulations
  220. In vivo translation rates can substantially delay the cotranslational folding of the Escherichia coli cytosolic proteome
  221. A Rationally Designed Six-Residue Swap Generates Comparability in the Aggregation Behavior of α-Synuclein and β-Synuclein
  222. Twisting Transition between Crystalline and Fibrillar Phases of Aggregated Peptides
  223. In support of the BMRB
  224. ADP ribosylation adapts an ER chaperone response to short-term fluctuations in unfolded protein load
  225. From Macroscopic Measurements to Microscopic Mechanisms of Protein Aggregation
  226. Sequence-Based Prediction of Protein Solubility
  227. Trigger Factor Slows Co-translational Folding through Kinetic Trapping while Sterically Protecting the Nascent Chain from Aberrant Cytosolic Interactions
  228. Determination of structural fluctuations of proteins from structure-based calculations of residual dipolar couplings
  229. Protein Structure Validation Using Side-Chain Chemical Shifts
  230. Structure of an Intermediate State in Protein Folding and Aggregation
  231. Proteome folding and aggregation
  232. Fibrillogenic propensity of the GroEL apical domain: A Janus-faced minichaperone
  233. Determination of Secondary Structure Populations in Disordered States of Proteins Using Nuclear Magnetic Resonance Chemical Shifts
  234. Characterization of the Conformational Equilibrium between the Two Major Substates of RNase A Using NMR Chemical Shifts
  235. Blind Testing of Routine, Fully Automated Determination of Protein Structures from NMR Data
  236. Prediction of variable translation rate effects on cotranslational protein folding
  237. Determination of Conformational Equilibria in Proteins Using Residual Dipolar Couplings
  238. Experimental free energy surfaces reveal the mechanisms of maintenance of protein solubility
  239. Coarse-grained model for protein folding based on structural profiles
  240. Inversion of the Balance between Hydrophobic and Hydrogen Bonding Interactions in Protein Folding and Aggregation
  241. ALS mutations in FUS cause neuronal dysfunction and death in Caenorhabditis elegans by a dominant gain-of-function mechanism
  242. Metastability of Native Proteins and the Phenomenon of Amyloid Formation
  243. Nucleated Polymerisation in the Presence of Pre-Formed Seed Filaments
  244. Using Side-Chain Aromatic Proton Chemical Shifts for a Quantitative Analysis of Protein Structures
  245. Using Side-Chain Aromatic Proton Chemical Shifts for a Quantitative Analysis of Protein Structures
  246. Excited-State Control of Protein Activity
  247. The A53T Mutation is Key in Defining the Differences in the Aggregation Kinetics of Human and Mouse α-Synuclein
  248. Nucleated polymerization with secondary pathways. II. Determination of self-consistent solutions to growth processes described by non-linear master equations
  249. Nucleated polymerization with secondary pathways. I. Time evolution of the principal moments
  250. Nucleated polymerization with secondary pathways. III. Equilibrium behavior and oligomer populations
  251. Protein Solubility and Protein Homeostasis: A Generic View of Protein Misfolding Disorders
  252. Using Chemical Shifts to Determine Structural Changes in Proteins upon Complex Formation
  253. Structure-based prediction of methyl chemical shifts in proteins
  254. The statistical theory of allostery
  255. 1H, 13C and 15N resonance assignments of human muscle acylphosphatase
  256. Asymmetric folding pathways and transient misfolding in a coarse-grained model of proteins
  257. Effects of the Known Pathogenic Mutations on the Aggregation Pathway of the Amyloidogenic Peptide of Apolipoprotein A-I
  258. Detection of early locomotor abnormalities in a Drosophila model of Alzheimer's disease
  259. Faculty Opinions recommendation of A transient and low-populated protein-folding intermediate at atomic resolution.
  260. On the Effect of the Ribosome and Trigger Factor on Nascent Chain Protein Folding
  261. New Scenarios of Protein Folding Can Occur on the Ribosome
  262. The iFly tracking system for an automated locomotor and behavioural analysis of Drosophila melanogaster
  263. Interactions in the native state of monellin, which play a protective role against aggregation
  264. Protein Dynamics: Moore's Law in Molecular Biology
  265. Amyloid-like Aggregates Sequester Numerous Metastable Proteins with Essential Cellular Functions
  266. Transient Tertiary Structure Formation within the Ribosome Exit Port
  267. Focus on Physical Principles of Protein Behavior in the Cell
  268. Structural characterization of a misfolded intermediate populated during the folding process of a PDZ domain
  269. Translationally optimal codons associate with aggregation-prone sites in proteins
  270. Accurate Determination of Interstrand Distances and Alignment in Amyloid Fibrils by Magic Angle Spinning NMR
  271. Proteome-Level Interplay between Folding and Aggregation Propensities of Proteins
  272. Enzymatic activity in disordered states of proteins
  273. Functional interactions as a survival strategy against abnormal aggregation
  274. Faculty Opinions recommendation of Widespread protein aggregation as an inherent part of aging in C. elegans.
  275. Using NMR Chemical Shifts as Structural Restraints in Molecular Dynamics Simulations of Proteins
  276. Physicochemical Determinants of Chaperone Requirements
  277. Time Averaging of NMR Chemical Shifts in the MLF Peptide in the Solid State
  278. Intrinsic Determinants of Neurotoxic Aggregate Formation by the Amyloid β Peptide
  279. Faculty Opinions recommendation of NMR spectroscopy brings invisible protein states into focus.
  280. Efficient identification of near-native conformations in ab initio protein structure prediction using structural profiles
  281. Derivation of a solubility condition for proteins from an analysis of the competition between folding and aggregation
  282. Determination of the Free Energy Landscape of α-Synuclein Using Spin Label Nuclear Magnetic Resonance Measurements
  283. An Analytical Solution to the Kinetics of Breakable Filament Assembly
  284. Accurate Random Coil Chemical Shifts from an Analysis of Loop Regions in Native States of Proteins
  285. Analysis of Sub-τc and Supra-τc Motions in Protein Gβ1 Using Molecular Dynamics Simulations
  286. Fast and Accurate Predictions of Protein NMR Chemical Shifts from Interatomic Distances
  287. On the Mechanism of Nonspecific Inhibitors of Protein Aggregation: Dissecting the Interactions of α-Synuclein with Congo Red and Lacmoid
  288. A Condensation-Ordering Mechanism in Nanoparticle-Catalyzed Peptide Aggregation
  289. Factors That Affect the Degree of Twist in β-Sheet Structures: A Molecular Dynamics Simulation Study of a Cross-β Filament of the GNNQQNY Peptide
  290. Physicochemical principles that regulate the competition between functional and dysfunctional association of proteins
  291. Physical Principles of Protein Behavior in the Cell
  292. Folding of Small Proteins by Monte Carlo Simulations with Chemical Shift Restraints without the Use of Molecular Fragment Replacement or Structural Homology
  293. Competition between Intramolecular and Intermolecular Interactions in an Amyloid-Forming Protein
  294. Position-Dependent Electrostatic Protection against Protein Aggregation
  295. A Relationship between mRNA Expression Levels and Protein Solubility in E. coli
  296. Mutational Analysis of the Aggregation-Prone and Disaggregation-Prone Regions of Acylphosphatase
  297. Toward an Accurate Determination of Free Energy Landscapes in Solution States of Proteins
  298. The mechanism of folding of Im7 reveals competition between functional and kinetic evolutionary constraints
  299. Factors That Affect the Degree of Twist in β-Sheet Structures: A Molecular Dynamics Simulation Study of a Cross-β Filament of the GNNQQNY Peptide
  300. Competition between Folding, Native-State Dimerisation and Amyloid Aggregation in β-Lactoglobulin
  301. Correlation between mRNA expression levels and protein aggregation propensities in subcellular localisations
  302. Quantitative approaches to defining normal and aberrant protein homeostasis
  303. Networks in Cell Biology
  304. Self-Templated Nucleation in Peptide and Protein Aggregation
  305. Comparison of successive transition states for folding reveals alternative early folding pathways of two homologous proteins
  306. Determination of Protein Structures in the Solid State from NMR Chemical Shifts
  307. Structure Determination of Protein−Protein Complexes Using NMR Chemical Shifts: Case of an Endonuclease Colicin−Immunity Protein Complex
  308. A Generic Mechanism of Emergence of Amyloid Protofilaments from Disordered Oligomeric Aggregates
  309. Inhibition of α-Synuclein Fibrillization by Dopamine Is Mediated by Interactions with Five C-Terminal Residues and with E83 in the NAC Region
  310. Introduction to the special issue of GENE
  311. A stochastic method for the reconstruction of protein structures from one-dimensional structural profiles
  312. Competition between protein aggregation and protein complex formation
  313. Structure and Dynamics of a Partially Folded Protein Are Decoupled from Its Mechanism of Aggregation
  314. ChemInform Abstract: The Zyggregator Method for Predicting Protein Aggregation Propensities
  315. Protein dynamics under light control
  316. Characterizing the First Steps of Amyloid Formation for the ccβ Peptide
  317. Prediction by Graph Theoretic Measures of Structural Effects in Proteins Arising from Non-Synonymous Single Nucleotide Polymorphisms
  318. Prediction of Aggregation-Prone Regions in Structured Proteins
  319. Mapping of Two Networks of Residues That Exhibit Structural and Dynamical Changes upon Binding in a PDZ Domain Protein
  320. Biological function in a non-native partially folded state of a protein
  321. A Coupled Equilibrium Shift Mechanism in Calmodulin-Mediated Signal Transduction
  322. Molecular determinants of the aggregation behavior of α- and β-synuclein
  323. Determination of the Transition State Ensemble for the Folding of Ubiquitin from a Combination of Φ and Ψ Analyses
  324. Characterisation of transition state structures for protein folding using 'high', 'medium' and 'low'  -values
  325. Towards quantitative predictions in cell biology using chemical properties of proteins
  326. The Zyggregator method for predicting protein aggregation propensities
  327. Stochastic reconstruction of protein structures from effective connectivity profiles
  328. Calculation of the free energy barriers in the oligomerisation of Ab
  329. Role of Intermolecular Forces in Defining Material Properties of Protein Nanofibrils
  330. The Distribution of Residues in a Polypeptide Sequence Is a Determinant of Aggregation Optimized by Evolution
  331. Influence of the fluctuations of the alignment tensor on the analysis of the structure and dynamics of proteins using residual dipolar couplings
  332. Systematic In Vivo Analysis of the Intrinsic Determinants of Amyloid β Pathogenicity
  333. Importance of Metastable States in the Free Energy Landscapes of Polypeptide Chains
  334. More charges against aggregation
  335. Characterisation of Amyloid Fibril Formation by Small Heat-shock Chaperone Proteins Human αA-, αB- and R120G αB-Crystallins
  336. Molecular dynamics simulations from putative transition states of α-spectrin SH3 domain
  337. Characterization of the nucleation barriers for protein aggregation and amyloid formation
  338. Protein structure determination from NMR chemical shifts
  339. Similarities in the thermodynamics and kinetics of aggregation of disease-related Aβ(1-40) peptides
  340. Life on the edge: a link between gene expression levels and aggregation rates of human proteins
  341. Determination of conformationally heterogeneous states of proteins
  342. Prediction of Local Structural Stabilities of Proteins from Their Amino Acid Sequences
  343. The MUMO (minimal under-restraining minimal over-restraining) method for the determination of native state ensembles of proteins
  344. A PDZ domain recapitulates a unifying mechanism for protein folding
  345. The Structurally Constrained Neutral Model of Protein Evolution
  346. Structural Reorganisation and Potential Toxicity of Oligomeric Species Formed during the Assembly of Amyloid Fibrils
  347. BPPred: A Web-based computational tool for predicting biophysical parameters of proteins
  348. Geometry, Energetics, and Dynamics of Hydrogen Bonds in Proteins:  Structural Information Derived from NMR Scalar Couplings
  349. STRUCTURAL BIOLOGY: Dynamic Visions of Enzymatic Reactions
  350. Characterization of the residual structure in the unfolded state of the Δ131Δ fragment of staphylococcal nuclease
  351. Relation between native ensembles and experimental structures of proteins
  352. Structural Comparison of the Two Alternative Transition States for Folding of TI I27
  353. Theoretical Approaches to Protein Aggregation
  354. Structural Interpretation of Hydrogen Exchange Protection Factors in Proteins: Characterization of the Native State Fluctuations of CI2
  355. Determination of an ensemble of structures representing the intermediate state of the bacterial immunity protein Im7
  356. Effective interactions between chaotropic agents and proteins
  357. Transition State Contact Orders Correlate with Protein Folding Rates
  358. Form of Growing Strings
  359. Determination of the folding transition states of barnase by using Φ I -value-restrained simulations validated by double mutant Φ IJ -values
  360. Interpreting Dynamically-Averaged Scalar Couplings in Proteins
  361. Prediction of “Aggregation-prone” and “Aggregation-susceptible” Regions in Proteins Associated with Neurodegenerative Diseases
  362. Comparison of Sequence-Based and Structure-Based Energy Functions for the Reversible Folding of a Peptide
  363. Detection of non-native hydrophobic interactions in the denatured state of lysozyme by molecular dynamics simulations
  364. A glimpse at the organization of the protein universe
  365. Formation of Native and Non-native Interactions in Ensembles of Denatured ACBP Molecules from Paramagnetic Relaxation Enhancement Studies
  366. Looking at structure, stability, and evolution of proteins through the principal eigenvector of contact matrices and hydrophobicity profiles
  367. Towards complete descriptions of the free–energy landscapes of proteins
  368. Simultaneous determination of protein structure and dynamics
  369. Protein folding and the organization of the protein topology universe
  370. Mapping Long-Range Interactions in α-Synuclein using Spin-Label NMR and Ensemble Molecular Dynamics Simulations
  371. Prediction of Site-Specific Amino Acid Distributions and Limits of Divergent Evolutionary Changes in Protein Sequences
  372. Principal eigenvector of contact matrices and hydrophobicity profiles in proteins
  373. Comparison of the Transition States for Folding of Two Ig-like Proteins from Different Superfamilies
  374. Prediction of the Absolute Aggregation Rates of Amyloidogenic Polypeptide Chains
  375. Low-populated folding intermediates of Fyn SH3 characterized by relaxation dispersion NMR
  376. Molecular Dynamics Studies of the Process of Amyloid Aggregation of Peptide Fragments of Transthyretin
  377. Determination of Protein Structures Consistent with NMR Order Parameters
  378. Reconstruction of Protein Structures from a Vectorial Representation
  379. Transition states for protein folding have native topologies despite high structural variability
  380. Determination of an Ensemble of Structures Representing the Denatured State of the Bovine Acyl-Coenzyme A Binding Protein
  381. Inhibition of protein crystallization by evolutionary negative design
  382. Comparison of the transition state ensembles for folding of Im7 and Im9 determined using all-atom molecular dynamics simulations with ϕ value restraints
  383. Rare Fluctuations of Native Proteins Sampled by Equilibrium Hydrogen Exchange
  384. Structures and relative free energies of partially folded states of proteins
  385. Statistical Properties of Neutral Evolution
  386. Calculation of Mutational Free Energy Changes in Transition States for Protein Folding
  387. Analysis of the distributed computing approach applied to the folding of a small β peptide
  388. Protein folding and misfolding: a paradigm of self–assembly and regulation in complex biological systems
  389. Connectivity of Neutral Networks, Overdispersion, and Structural Conservation in Protein Evolution
  390. Protein folding: bringing theory and experiment closer together
  391. Self-consistent determination of the transition state for protein folding: Application to a fibronectin type III domain
  392. Validity of Gō Models: Comparison with a Solvent-Shielded Empirical Energy Decomposition
  393. Determination of the structures of distinct transition state ensembles for a β-sheet peptide with parallel folding pathways
  394. Determination of a Transition State at Atomic Resolution from Protein Engineering Data
  395. Lack of Self-Averaging in Neutral Evolution of Proteins
  396. Small-world view of the amino acids that play a key role in protein folding
  397. Native and non-native interactions along protein folding and unfolding pathways
  398. Statistical properties of contact vectors
  399. Automated assignment of SCOP and CATH protein structure classifications from FSSP scores
  400. Energetics of enzyme stability
  401. Three key residues form a critical contact network in a protein folding transition state
  402. How to guarantee optimal stability for most representative structures in the protein data bank
  403. Comparison of two optimization methods to derive energy parameters for protein folding: Perceptron and Z score
  404. Toward an energy function for the contact map representation of proteins
  405. Toward an energy function for the contact map representation of proteins
  406. Structurally constrained protein evolution: results from a lattice simulation
  407. A statistical mechanical method to optimize energy functions for protein folding
  408. Can a pairwise contact potential stabilize native protein folds against decoys obtained by threading?
  409. Protein folding using contact maps
  410. Comparison of two optimization methods to derive energy parameters for protein folding: Perceptron andZ score
  411. Folding Lennard-Jones proteins by a contact potential
  412. Neutral Evolution of Model Proteins: Diffusion in Sequence Space and Overdispersion
  413. Hydrophobicity and unique folding of selected polymers
  414. Protein Folding in Contact Map Space
  415. Statistical properties of contact maps
  416. An optimal derivation of a potential for protein folding
  417. Pairwise contact potentials are unsuitable for protein folding
  418. Efficient dynamics in the space of contact maps
  419. High-Dimensional Bak-Sneppen Model
  420. Protein stability and foldability–designability complementarity
  421. Recovery of protein structure from contact maps
  422. Stability Threshold as a Selection Principle for Protein Design
  423. Growth with memory
  424. Modified configurational bias Monte Carlo method for simulation of polymer systems
  425. Model of correlated evolution
  426. Hot sandpiles
  427. Optimal Protein Design Procedure
  428. Diffusion in disordered media as a process with memory
  429. Disordered flat phase and phase diagram for restricted solid-on-solid models of fcc (110) surfaces
  430. Quenched disorder, memory, and self-organization
  431. Evolution of the missing row deconstruction on Rh (110)
  432. A mean-field study of the temperature dependence of the layer magnetizations in a semi-infinite ising model
  433. Magnetic-Phase Transitions of Ising Surfaces with Modified Surface-Bulk Coupling: a Monte Carlo Study
  434. Network views of the cell
  435. Introduction
  436. Protein folding using inter-residue contact