4.7 Article

MEERCAT: Multiplexed Efficient Cell Free Expression of Recombinant QconCATs For Large Scale Absolute Proteome Quantification

Journal

MOLECULAR & CELLULAR PROTEOMICS
Volume 16, Issue 12, Pages 2169-2183

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/mcp.RA117.000284

Keywords

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Funding

  1. Biotechnology and Biological Sciences Research Council international ITAS grant [BB/R005311/1]
  2. JSPS KAKENHI [16K08937]
  3. Biotechnology and Biological Sciences Research Council [BB/R005311/1, BB/J002631/1] Funding Source: researchfish
  4. Medical Research Council [MR/M009114/1] Funding Source: researchfish
  5. BBSRC [BB/J002631/1, BB/R005311/1] Funding Source: UKRI
  6. MRC [MR/M009114/1] Funding Source: UKRI
  7. Grants-in-Aid for Scientific Research [16K08937] Funding Source: KAKEN

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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.

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