TY - JOUR
T1 - Cell-free cotranslation and selection using in vitro virus for high-throughput analysis of protein-protein interactions and complexes
AU - Miyamoto-Sato, Etsuko
AU - Ishizaka, Masamichi
AU - Horisawa, Kenichi
AU - Tateyama, Seiji
AU - Takashima, Hideaki
AU - Fuse, Shinichiro
AU - Sue, Kaori
AU - Hirai, Naoya
AU - Masuoka, Kazuyo
AU - Yanagawa, Hiroshi
PY - 2005/5
Y1 - 2005/5
N2 - 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.
AB - 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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U2 - 10.1101/gr.3510505
DO - 10.1101/gr.3510505
M3 - Article
C2 - 15867431
AN - SCOPUS:21144480358
SN - 1088-9051
VL - 15
SP - 710
EP - 717
JO - Genome Research
JF - Genome Research
IS - 5
ER -