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通过竞争活性蛋白质谱分析策略探索顺铂在 HeLa 细胞中的分子靶标。

Molecular targets of cisplatin in HeLa cells explored through competitive activity-based protein profiling strategy.

机构信息

Tongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan 430030, China.

Tongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

J Inorg Biochem. 2024 May;254:112518. doi: 10.1016/j.jinorgbio.2024.112518. Epub 2024 Mar 6.

Abstract

Cisplatin is widely used as anticancer drugs, and DNA is considered as the main target. Considering its high affinity towards cysteines and the important role of cystine containing proteins, we applied a competitive activity-based protein profiling strategy to identify protein cysteines that bind with cisplatin in HeLa cells. Living cells were treated with cisplatin at cytotoxic concentrations, then the protein was extracted. After labeling with desthiobiotin iodoacetamide (DBIA) probe, protein was precipitated, digested and isotopically labeled, subsequently the peptides were combined, and the biotinylated cysteine-containing peptides were enriched and quantified by LC-MS/MS. A total of 3571 peptides which originated from 1871 proteins were identified using the DBIA probe. Among them, 46 proteins were screened as targets, including proteins that have been identified as binding proteins by previous study. A novel cisplatin target, calpain-1 (CAPN1), was identified and validated as binding with cisplatin in vitro.

摘要

顺铂被广泛用作抗癌药物,而 DNA 被认为是其主要靶点。考虑到顺铂与半胱氨酸的高亲和力以及含胱氨酸蛋白质的重要作用,我们应用竞争性基于活性的蛋白质谱分析策略来鉴定与 HeLa 细胞中的顺铂结合的蛋白质半胱氨酸。用细胞毒性浓度的顺铂处理活细胞,然后提取蛋白质。用去硫生物素碘乙酰胺(DBIA)探针标记后,沉淀蛋白质,消化并进行同位素标记,然后将肽组合,通过 LC-MS/MS 对含生物素的半胱氨酸肽进行富集和定量。使用 DBIA 探针鉴定出了 3571 条来自 1871 种蛋白质的肽。其中,筛选出 46 种作为靶标的蛋白质,包括以前的研究已经确定为结合蛋白的蛋白质。鉴定并验证了一种新型顺铂靶标钙蛋白酶 1(CAPN1)与顺铂在体外结合。

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