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