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DOI码：

10.1016/j.mcpro.2025.101494

发表刊物：

Molecular & Cellular Proteomics

关键字：

post-translational modification (PTM); PTM crosstalk; peptide identification; computational proteomics; mixed integer linear programming (MILP)

摘要：

Post-translational modifications (PTMs) are pivotal in cellular regulations, and their crosstalk is related to various diseases such as cancer. Given the prevalence of PTM crosstalk within close amino acid ranges, identifying peptides with multiple PTMs is essential. However, this task is an NP-hard combinatorial problem with exponential complexity, posing significant challenges for existing analysis methods. Here, we introduce PIPI-C (PTM-Invariant Peptide Identification with a Combinatorial model), a novel search engine that addresses this challenge through a mixed integer linear programming (MILP) model, thereby overcoming the limitations of existing approaches that struggle with high-order PTM combinations. Rigorous validation across diverse datasets confirms PIPI-C’s superior performance in detecting PTM combinations. When applied to over 72 million mass spectra of three human cancers—lung squamous cell carcinoma (LSCC), colorectal adenocarcinoma (COAD), and glioblastoma (GBM)—PIPI-C reveals significantly upregulated PTM combinations. In LSCC, 50% of 860 upregulated unique PTM site patterns (UPSPs) (when comparing cancer vs. normal samples) carried at least two PTMs, including literature-supported crosstalks such as di-methylation with trifluoroleucine substitution and amidation with proline-to-valine substitution. Similar findings in COAD and GBM highlight PIPI-C’s utility in uncovering cancer-relevant PTM combination landscapes. Overall, PIPI-C provides a robust mathematical framework for decoding complex PTM patterns, advancing our understanding of PTM-driven cellular processes in diseases.

合写作者：

Peize Zhao, Chen Zhou, Ning Li, Weichuan Yu

第一作者：

Shengzhi Lai#, Shuaijian Dai#

论文类型：

期刊论文

文献类型：

Article

卷号：

25

期号：

2

页面范围：

101494

ISSN号：

1535-9476

是否译文：

否

发表时间：

2025-12-23