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Cell-free cotranslation and selection using in vitro virus for high-throughput analysis of protein–protein interactions and complexes
Author(s) -
Etsuko MiyamotoSato,
Masamichi Ishizaka,
Kenichi Horisawa,
Seiji Tateyama,
Hideaki Takashima,
Shinichiro Fuse,
Kaori Sue,
Naoya Hirai,
Kazuyo Masuoka,
Hiroshi Yanagawa
Publication year - 2005
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.3510505
Subject(s) - biology , in vitro , computational biology , leucine zipper , selection (genetic algorithm) , complementary dna , cell free system , microbiology and biotechnology , genetics , peptide sequence , gene , computer science , artificial intelligence
We have developed a simple and totally in vitro selection procedure based on cell-free cotranslation using a highly stable and efficient in vitro virus (IVV). Cell-free cotranslation of tagged bait and prey proteins is advantageous for the formation of protein complexes and allows high-throughput analysis of protein-protein interactions (PPI) as a result of providing in vitro instead of in vivo preparation of bait proteins. The use of plural selection rounds and a two-step purification of the IVV selection, followed by in vitro post-selection, is advantageous for decreasing false positives. In a single experiment using bait Fos, more than 10 interactors, including not only direct, but also indirect interactions, were enriched. Further, previously unidentified proteins containing novel leucine zipper (L-ZIP) motifs with minimal binding sites identified by sequence alignment as functional elements were detected as a result of using a randomly primed cDNA library. Thus, we consider that this simple IVV selection system based on cell-free cotranslation could be applicable to high-throughput and comprehensive analysis of PPI and complexes in large-scale settings involving parallel bait proteins.

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