All Stories

  1. A bacterial dual positive and negative selection system for dCas9 activity
  2. On the role of alginate structure in complexing with lysozyme and application for enzyme delivery
  3. Environmental changes bridge evolutionary valleys
  4. Enzymatic protein switches built from paralogous input domains
  5. Electrochemical activation of engineered protein switches
  6. Design of protein switches based on an ensemble model of allostery
  7. Rational Design of a Fusion Protein to Exhibit Disulfide-Mediated Logic Gate Behavior
  8. Characterization of Monobody Scaffold Interactions with Ligand via Force Spectroscopy and Steered Molecular Dynamics
  9. Advancements in the Development of HIF-1α-Activated Protein Switches for Use in Enzyme Prodrug Therapy
  10. The thymidylate kinase genes from Mycobacterium tuberculosis and methicillin-resistant Staphylococcus aureus confer 3′-azido-3′-deoxythymidine resistance to Escherichia coli
  11. Directed Evolution of Improved Zinc Finger Methyltransferases
  12. Correction: Targeted DNA Methylation Using an Artificially Bisected M.HhaI Fused to Zinc Fingers
  13. The High-Affinity Maltose Switch MBP317-347 has Low Affinity for Glucose: Implications for Targeting Tumors with Metabolically Directed Enzyme Prodrug Therapy
  14. Non-allosteric enzyme switches possess larger effector-induced changes in thermodynamic stability than their non-switch analogs
  15. Protein Switch Engineering by Domain Insertion
  16. PFunkel: Efficient, Expansive, User-Defined Mutagenesis
  17. Targeted DNA Methylation Using an Artificially Bisected M.HhaI Fused to Zinc Fingers
  18. Structure of an Engineered β-Lactamase Maltose Binding Protein Fusion Protein: Insights into Heterotropic Allosteric Regulation
  19. A Hot-Spot Motif Characterizes the Interface between a Designed Ankyrin-Repeat Protein and Its Target Ligand
  20. In Vitro Recombination of Non-Homologous Genes Can Result in Gene Fusions that Confer a Switching Phenotype to Cells
  21. Molecular Imprinting of Maltose Binding Protein: Tuning Protein Recognition at the Molecular Level
  22. Abstract 536: A hypoxia-activated protein switch as a potential anticancer therapeutic
  23. Circular Permutation of Proteins
  24. Surface-tethered protein switches
  25. Sites in the AAV5 capsid tolerant to deletions and tandem duplications
  26. Designing switchable enzymes
  27. Design and synthesis of a β-lactamase activated 5-fluorouracil prodrug
  28. Morphogen-defined patterning of Escherichia coli enabled by an externally tunable band-pass filter
  29. An engineered split M.HhaI-zinc finger fusion lacks the intended methyltransferase specificity
  30. Structure Prediction of Domain Insertion Proteins from Structures of Individual Domains
  31. Directed evolution for drug and nucleic acid delivery
  32. As easy as flipping a switch?
  33. Ligand binding and allostery can emerge simultaneously
  34. Beyond Cataloging the Library of Babel
  35. Modulation of effector affinity by hinge region mutations also modulates switching activity in an engineered allosteric TEM1 β-lactamase switch
  36. Enhanced Catalytic Efficiency of Aminoglycoside Phosphotransferase (3′)-IIa Achieved Through Protein Fragmentation and Reassembly
  37. Protein fragment complementation in M.HhaI DNA methyltransferase
  38. Mathematical expressions useful in the construction, description and evaluation of protein libraries
  39. A Molecular Switch Created by In Vitro Recombination of Nonhomologous Genes
  40. Creation of an Allosteric Enzyme by Domain Insertion
  41. Construction of Protein Fragment Complementation Libraries Using Incremental Truncation
  42. Synthetic gene libraries: in search of the optimal diversity
  43. Theoretical distribution of truncation lengths in incremental truncation libraries
  44. Evolution of protein function by Domain swapping
  45. A two-phagemid system for the creation of non-phage displayed antibody libraries approaching one trillion members
  46. Incremental truncation as a strategy in the engineering of novel biocatalysts
  47. Hybrid enzymes: manipulating enzyme design
  48. Folding and aggregation of TEM β-lactamase: Analogies with the formation of inclusion bodies inEscherichia coli
  49. The Creation of ITCHY Hybrid Protein Libraries
  50. Preparation of SCRATCHY Hybrid Protein Libraries Size- and In-Frame Selection of Nucleic Acid Sequences