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展示大规模开发标准化检测方法以定量测定人体蛋白质的可行性。

Demonstrating the feasibility of large-scale development of standardized assays to quantify human proteins.

机构信息

Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.

出版信息

Nat Methods. 2014 Feb;11(2):149-55. doi: 10.1038/nmeth.2763. Epub 2013 Dec 8.

Abstract

Multiple reaction monitoring (MRM) mass spectrometry has been successfully applied to monitor targeted proteins in biological specimens, raising the possibility that assays could be configured to measure all human proteins. We report the results of a pilot study designed to test the feasibility of a large-scale, international effort for MRM assay generation. We have configured, validated across three laboratories and made publicly available as a resource to the community 645 novel MRM assays representing 319 proteins expressed in human breast cancer. Assays were multiplexed in groups of >150 peptides and deployed to quantify endogenous analytes in a panel of breast cancer-related cell lines. The median assay precision was 5.4%, with high interlaboratory correlation (R(2) > 0.96). Peptide measurements in breast cancer cell lines were able to discriminate among molecular subtypes and identify genome-driven changes in the cancer proteome. These results establish the feasibility of a large-scale effort to develop an MRM assay resource.

摘要

多反应监测 (MRM) 质谱法已成功应用于监测生物标本中的靶向蛋白,这使得检测方法有可能被配置为测量所有人类蛋白质。我们报告了一项旨在测试大规模国际 MRM 检测生成工作可行性的试点研究的结果。我们已经配置了 319 种在人类乳腺癌中表达的蛋白质的 645 种新型 MRM 检测方法,并在三个实验室进行了验证,然后将其作为社区资源公开发布。检测方法以 >150 个肽的组进行多重检测,并部署用于定量乳腺癌相关细胞系中内源性分析物。检测方法的中位数精度为 5.4%,具有很高的实验室间相关性(R(2) > 0.96)。乳腺癌细胞系中的肽测量能够区分分子亚型,并确定癌症蛋白质组中的基因组驱动变化。这些结果证实了进行大规模开发 MRM 检测方法资源的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce53/3922286/fd7e41aab478/nihms540682f1.jpg

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