基于尖端强阳离子交换色谱法从 LysargiNase 消化液中分离蛋白质 N 端肽的一步式 N 端组学。

IF 6.1 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Molecular & Cellular Proteomics Pub Date : 2024-09-01 Epub Date: 2024-07-26 DOI:10.1016/j.mcpro.2024.100820
Kazuya Morikawa, Hiroshi Nishida, Koshi Imami, Yasushi Ishihama
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引用次数: 0

摘要

我们开发了一种基于吸头的强阳离子交换(SCX)色谱从 LysargiNase 消化液中一步分离蛋白质 N 端肽的方法。这种 CHAMP-N(蛋白质 N 端肽的色谱放大)方法使用一次性、可并行处理的 SCX 吸头代替传统的 HPLC SCX 色谱柱,有利于进行简单、灵敏、可重现和高通量的 N 端组学分析,而不会牺牲基于 HPLC 方法所实现的高鉴定数和选择性。通过在 HEK293T 细胞中应用 CHAMP-N 方法,我们确定了信号肽和转运肽的新裂解位点以及非经典翻译起始位点。最后,对于全蛋白质组的端粒组学,我们介绍了一种简单而全面的 N 端和 C 端粒组学平台,该平台采用了三种不同的基于尖端的方法,包括 CHAMP-N,其中蛋白酶消化和尖端 LC 一步分离常用于实现互补的端粒组覆盖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
One-step N-Terminomics Based on Isolation of Protein N-Terminal Peptides From LysargiNase Digests by Tip-Based Strong Cation Exchange Chromatography.

We have developed a one-step isolation method for protein N-terminal peptides from LysargiNase digests by pipette tip-based strong cation exchange (SCX) chromatography. This CHAMP-N (CHromatographic AMplification of Protein N-terminal peptides) method using disposable and parallel-processable SCX tips instead of conventional HPLC SCX columns facilitates simple, sensitive, reproducible, and high-throughput N-terminomic profiling without sacrificing the high identification numbers and selectivity achieved by the HPLC-based method. By applying the CHAMP-N method to HEK293T cells, we identified novel cleavage sites for signal and transit peptides and non-canonical translation initiation sites. Finally, for proteome-wide terminomics, we present a simple and comprehensive N- and C-terminomics platform employing three different tip-based approaches, including CHAMP-N, in which protease digestion and one-step isolation by tip LC are commonly used to achieve complementary terminome coverages.

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来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
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