Directed Evolution of Proteins throughIn VitroProtein Synthesis in Liposomes
Author(s) -
Takehiro Nishikawa,
Takeshi Sunami,
Tomoaki Matsuura,
Tetsuya Yomo
Publication year - 2012
Publication title -
journal of nucleic acids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.621
H-Index - 32
eISSN - 2090-021X
pISSN - 2090-0201
DOI - 10.1155/2012/923214
Subject(s) - liposome , in vitro , directed evolution , directed molecular evolution , computational biology , green fluorescent protein , systematic evolution of ligands by exponential enrichment , biology , gene , recombinant dna , microbiology and biotechnology , chemistry , biochemistry , rna , mutant
Directed evolution of proteins is a technique used to modify protein functions through “Darwinian selection.” In vitro compartmentalization (IVC) is an in vitro gene screening system for directed evolution of proteins. IVC establishes the link between genetic information (genotype) and the protein translated from the information (phenotype), which is essential for all directed evolution methods, by encapsulating both in a nonliving microcompartment. Herein, we introduce a new liposome-based IVC system consisting of a liposome, the protein synthesis using recombinant elements (PURE) system and a fluorescence-activated cell sorter (FACS) used as a microcompartment, in vitro protein synthesis system, and high-throughput screen, respectively. Liposome-based IVC is characterized by in vitro protein synthesis from a single copy of a gene in a cell-sized unilamellar liposome and quantitative functional evaluation of the synthesized proteins. Examples of liposome-based IVC for screening proteins such as GFP and β -glucuronidase are described. We discuss the future directions for this method and its applications.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom