Back to Search
Start Over
Statistical Coupling Analysis-Guided Library Design for the Discovery of Mutant Luciferases.
- Source :
-
Biochemistry [Biochemistry] 2018 Feb 06; Vol. 57 (5), pp. 663-671. Date of Electronic Publication: 2017 Dec 28. - Publication Year :
- 2018
-
Abstract
- Directed evolution has proven to be an invaluable tool for protein engineering; however, there is still a need for developing new approaches to continue to improve the efficiency and efficacy of these methods. Here, we demonstrate a new method for library design that applies a previously developed bioinformatic method, Statistical Coupling Analysis (SCA). SCA uses homologous enzymes to identify amino acid positions that are mutable and functionally important and engage in synergistic interactions between amino acids. We use SCA to guide a library of the protein luciferase and demonstrate that, in a single round of selection, we can identify luciferase mutants with several valuable properties. Specifically, we identify luciferase mutants that possess both red-shifted emission spectra and improved stability relative to those of the wild-type enzyme. We also identify luciferase mutants that possess a >50-fold change in specificity for modified luciferins. To understand the mutational origin of these improved mutants, we demonstrate the role of mutations at N229, S239, and G246 in altered function. These studies show that SCA can be used to guide library design and rapidly identify synergistic amino acid mutations from a small library.
- Subjects :
- Amino Acid Sequence
Amino Acid Substitution
Amino Acids chemistry
Animals
Computational Biology methods
Drug Design
Drug Discovery
Fireflies enzymology
Luciferases, Firefly chemistry
Luciferases, Firefly radiation effects
Models, Molecular
Protein Conformation
Protein Stability
Sequence Alignment
Sequence Homology, Amino Acid
Substrate Specificity
Fireflies genetics
Gene Library
Genes, Insect
Luciferases, Firefly genetics
Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4995
- Volume :
- 57
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 29224332
- Full Text :
- https://doi.org/10.1021/acs.biochem.7b01014