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MEERCAT: Multiplexed Efficient Cell Free Expression of Recombinant QconCATs For Large Scale Absolute Proteome Quantification.
Takemori, Nobuaki; Takemori, Ayako; Tanaka, Yuki; Endo, Yaeta; Hurst, Jane L; Gómez-Baena, Guadalupe; Harman, Victoria M; Beynon, Robert J.
Afiliação
  • Takemori N; From the ‡Proteo-Science Center, Ehime University, Ehime, 791-0295, Japan; r.beynon@liverpool.ac.uk takemori@m.ehime-u.ac.jp.
  • Takemori A; §Advanced Research Support Center, Ehime University, Ehime, 791-0295, Japan.
  • Tanaka Y; From the ‡Proteo-Science Center, Ehime University, Ehime, 791-0295, Japan.
  • Endo Y; ¶The United Graduate School of Agricultural Sciences, Ehime University, Ehime, 790-8566, Japan.
  • Hurst JL; §Advanced Research Support Center, Ehime University, Ehime, 791-0295, Japan.
  • Gómez-Baena G; From the ‡Proteo-Science Center, Ehime University, Ehime, 791-0295, Japan.
  • Harman VM; **Mammalian Behaviour and Evolution Group, Institute of Integrative Biology, University of Liverpool, Leahurst Campus, Neston CH64 7TE.
  • Beynon RJ; ‖Centre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, UK.
Mol Cell Proteomics ; 16(12): 2169-2183, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29055021
A major challenge in proteomics is the absolute accurate quantification of large numbers of proteins. QconCATs, artificial proteins that are concatenations of multiple standard peptides, are well established as an efficient means to generate standards for proteome quantification. Previously, QconCATs have been expressed in bacteria, but we now describe QconCAT expression in a robust, cell-free system. The new expression approach rescues QconCATs that previously were unable to be expressed in bacteria and can reduce the incidence of proteolytic damage to QconCATs. Moreover, it is possible to cosynthesize QconCATs in a highly-multiplexed translation reaction, coexpressing tens or hundreds of QconCATs simultaneously. By obviating bacterial culture and through the gain of high level multiplexing, it is now possible to generate tens of thousands of standard peptides in a matter of weeks, rendering absolute quantification of a complex proteome highly achievable in a reproducible, broadly deployable system.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Sistema Livre de Células / Proteômica Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Sistema Livre de Células / Proteômica Idioma: En Ano de publicação: 2017 Tipo de documento: Article