| Literature DB >> 25055787 |
Julian Zaugg1, Yosephine Gumulya, Elizabeth M J Gillam, Mikael Bodén.
Abstract
Directed evolution methods have proved to be highly effective in the design of novel proteins and in the generation of large libraries of diverse sequences. However, searching through the vast number of mutants produced during such experiments in order to find the best represents a daunting and difficult task. In recent years, a number of computational tools have been developed to provide guidance during this exploratory process. It can, however, be unclear as to which tool or tools best complement the chosen library design strategy. In this review, we describe and critically evaluate some of the more notable tools in this area, discussing the rationale behind each, the requirements for their implementation, and potential issues faced when using them. Some examples of their application in an experimental setting are also provided. The tools have been classified based on contrasting strategies as to how they function: prospective tools SCHEMA and OPTCOMB use extant sequence and structural data to predict optimal locations for crossover sites, whereas retrospective tools ProSAR and ASRA use property data from the mutant library to predict beneficial mutations and features. From our evaluation, we suggest that each tool can play a role in the design process; however this is largely dictated by the data available and the desired experimental strategy for the project.Mesh:
Year: 2014 PMID: 25055787 DOI: 10.1007/978-1-4939-1053-3_21
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745