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21-plex DiLeu 同重标记试剂用于高通量定量蛋白质组学。

21-plex DiLeu Isobaric Tags for High-Throughput Quantitative Proteomics.

机构信息

School of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705, United States.

Department of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.

出版信息

Anal Chem. 2020 Jun 16;92(12):8228-8234. doi: 10.1021/acs.analchem.0c00473. Epub 2020 May 28.

DOI:10.1021/acs.analchem.0c00473
PMID:32401496
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7306224/
Abstract

Isobaric tags enable multiplexed quantitative analysis of many biological samples in a single LC-MS/MS experiment. As a cost-effective alternative to expensive commercial isobaric tagging reagents, we developed our own custom ,-dimethylleucine "DiLeu" isobaric tags for quantitative proteomics. Here, we present a new generation of DiLeu tags that achieves 21-plex quantification in high-resolution HCD MS/MS spectra via distinct reporter ions that differ in mass from each other by a minimum of 3 mDa. The 21-plex set retains the compact tag structure and existing isotopologues of the 12-plex set but includes nine new reporter variants formulated with unique configurations of C, N, and H stable isotopes, each synthesized in-house via a stepwise -monomethylation synthesis strategy using readily available reagents. Thus, multiplexing capacity is expanded significantly, while preserving the performance and low cost of the previous implementation. We show that 21-plex DiLeu tags generate strong reporter ions following HCD fragmentation of labeled peptides acquired on Orbitrap platforms at a minimum of 60,000 resolving power (at 400 /), and we demonstrate accurate 21-plex quantification of labeled K562 human cell line protein digests via single-shot nanoLC-MS/MS analysis on a Q Exactive HF system.

摘要

同重标记试剂可实现单个 LC-MS/MS 实验中对多个生物样本的多重定量分析。作为昂贵的商业同重标记试剂的经济有效的替代方法,我们开发了自己定制的 -二甲基亮氨酸“DiLeu”同重标记试剂,用于定量蛋白质组学。在这里,我们提出了新一代的 DiLeu 标签,通过质量相差至少 3 mDa 的独特报告离子,在高分辨率 HCD MS/MS 谱中实现 21 重定量。21 重集保留了 12 重集的紧凑标签结构和现有同位素,但包括九个新的报告变体,这些变体采用 C、N 和 H 稳定同位素的独特构型配制,每个变体都通过使用市售试剂的逐步单甲基化合成策略在内部合成。因此,在保留先前实现的性能和低成本的同时,大大扩展了多重化能力。我们表明,21 重 DiLeu 标签在 Orbitrap 平台上获取的标记肽经 HCD 碎裂后生成强报告离子,在 60,000 分辨率(在 400 /m)下最少,并且我们通过在 Q Exactive HF 系统上进行单次纳米 LC-MS/MS 分析,证明了对标记的 K562 人细胞系蛋白消化物进行准确的 21 重定量。

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