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基于 Tip 型强阳离子交换层析从赖氨酰内肽酶消化产物中分离蛋白 N 末端肽的一步 N 端组学分析。

One-step N-Terminomics Based on Isolation of Protein N-Terminal Peptides From LysargiNase Digests by Tip-Based Strong Cation Exchange Chromatography.

机构信息

Department of Molecular Systems BioAnalysis, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.

Department of Molecular Systems BioAnalysis, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan; Proteome Homeostasis Research Unit, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.

出版信息

Mol Cell Proteomics. 2024 Sep;23(9):100820. doi: 10.1016/j.mcpro.2024.100820. Epub 2024 Jul 26.

DOI:10.1016/j.mcpro.2024.100820
PMID:39069075
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11382313/
Abstract

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.

摘要

我们开发了一种一步法从赖氨酰内肽酶消化物中分离蛋白质 N 端肽的方法,基于移液器吸头的强阳离子交换(SCX)色谱。这种 CHAMP-N(蛋白质 N 端肽的色谱扩增)方法使用一次性且可并行处理的 SCX 吸头代替传统的 HPLC SCX 柱,可实现简单、灵敏、可重现和高通量的 N 端组学分析,而不会牺牲基于 HPLC 方法获得的高鉴定数量和选择性。通过将 CHAMP-N 方法应用于 HEK293T 细胞,我们鉴定了信号肽和转运肽以及非典型翻译起始位点的新切割位点。最后,为了进行全蛋白质组学的端肽组学分析,我们提出了一种简单而全面的 N 端和 C 端组学平台,采用三种不同的基于吸头的方法,包括 CHAMP-N,其中蛋白酶消化和一步通过吸头 LC 分离通常用于实现互补的端肽覆盖率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/264577038074/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/999beb716cbe/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/112b908ff1bb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/f4775c9206af/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/9170815c8069/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/14ab5f771ad2/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/264577038074/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/999beb716cbe/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/112b908ff1bb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/f4775c9206af/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/9170815c8069/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/14ab5f771ad2/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc0/11382313/264577038074/gr5.jpg

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