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Human protein factory for converting the transcriptome into an in vitro-expressed proteome

Authors :
Kiyoshi Matsuo
Yasutomo Kisu
Kazuhide Yahata
Tsuyoshi Sumiya
Atsushi Murase
Saki Sono
Riyo Morishita
Toshihiro Kuroita
Naoko Kagawa
Kouichi Kimura
Kazuyoshi Minami
Ryohei Satoh
Yaeta Endo
Shinya Watanabe
Mariko Mitsubori
Nobuo Nomura
Miki Kobayashi
Tetsuo Nishikawa
Junichi Yamamoto
Yoshifumi Kawamura
Toshihiko Okamoto
Keiichi Kanehori
Fumio Imamoto
Aya Miura
Hiroyuki Takeda
Akiko Fukumoto
Reiko Honma
Yukio Maruyama
Naoki Goshima
Hisashi Kuwayama
Yuki Iida
Yuka Yanagisawa
Noriko Sakagami
Akira Nishikawa
Masatoshi Mori
Yukiko Takayama
Shigeo Tanaka
Hiroko Yamada
Kumiko Ishikawa
Ai Wakamatsu
Rie Kimura
Shigemichi Nishikawa
Akio Sugiyama
Chie Kaminaga
Kiyokazu Kenmochi
Yukari Sasaki
Bunsei Kawakami
Taichi Andoh
Takao Isogai
Emi Ito
Takushi Togashi
Tomoko Takayama
Tomoe Seki
Yutaka Sakamoto
Jun-ichi Imai
Source :
Nature methods. 5(12)
Publication Year :
2008

Abstract

Appropriate resources and expression technology necessary for human proteomics on a whole-proteome scale are being developed. We prepared a foundation for simple and efficient production of human proteins using the versatile Gateway vector system. We generated 33,275 human Gateway entry clones for protein synthesis, developed mRNA expression protocols for them and improved the wheat germ cell-free protein synthesis system. We applied this protein expression system to the in vitro expression of 13,364 human proteins and assessed their biological activity in two functional categories. Of the 75 tested phosphatases, 58 (77%) showed biological activity. Several cytokines containing disulfide bonds were produced in an active form in a nonreducing wheat germ cell-free expression system. We also manufactured protein microarrays by direct printing of unpurified in vitro-synthesized proteins and demonstrated their utility. Our 'human protein factory' infrastructure includes the resources and expression technology for in vitro proteome research.

Details

ISSN :
15487105
Volume :
5
Issue :
12
Database :
OpenAIRE
Journal :
Nature methods
Accession number :
edsair.doi.dedup.....37544d5fae7b300fe8f01e3359f7b56c