The Mtb Proteome Library: A Resource of Assays to Quantify the Complete Proteome of Mycobacterium tuberculosis

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• 作者：Olga T. Schubert¹ ; ² ; Jeppe Mouritsen¹ ; ³ ; Christina Ludwig¹ ; Hannes L. Rö ; st¹ ; ² ; George Rosenberger¹ ; ² ; Patrick K. Arthur⁴ ; Manfred Claassen¹ ; David S. Campbell⁵ ; Zhi Sun⁵ ; Terry Farrah⁵ ; Martin Gengenbacher⁶ ; Alessio Maiolica¹ ; Stefan H.E. Kaufmann⁶ ; Robert L. Moritz⁵ ; Ruedi Aebersold¹ ; ⁷ ; ^{aebersold@imsb.biol.ethz.ch}
• 刊名：Cell Host Microbe
• 出版年：2013
• 出版时间：15 May, 2013
• 年：2013
• 卷：13
• 期：5
• 页码：602-612
• 全文大小：1335 K

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class=""h3"">Summary

Research advancing our understanding of Mycobacterium tuberculosis (Mtb) biology and complex host-Mtb interactions requires consistent and precise quantitative measurements of Mtb proteins. We describe the generation and validation of a compendium of assays to quantify 97 % of the 4,012 annotated Mtb proteins by the targeted mass spectrometric method selected reaction monitoring (SRM). Furthermore, we estimate the absolute abundance for 55 % of all Mtb proteins, revealing a dynamic range within the Mtb proteome of over four orders of magnitude, and identify previously unannotated proteins. As an example of the assay library utility, we monitored the entire Mtb dormancy survival regulon (DosR), which is linked to anaerobic survival and Mtb persistence, and show its dynamic protein-level regulation during hypoxia. In conclusion, we present a publicly available research resource that supports the sensitive, precise, and reproducible quantification of virtually any Mtb protein by a robust and widely accessible mass spectrometric method.