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通过基于位点和结构的 N-糖蛋白质组学研究,鉴定到乳腺癌多药耐药 MCF-7 腺癌细胞和肿瘤干细胞中的糖基化获得。

Gain-of-glycosylation in breast multi-drug-resistant MCF-7 adenocarcinoma cells and cancer stem cells characterized by site- and structure-specific N-glycoproteomics.

机构信息

School of Chemical Science & Engineering, Shanghai Key Laboratory of Chemical Assessment and Sustainability, Tongji University, Shanghai, 200092, China.

School of Chemical Science & Engineering, Shanghai Key Laboratory of Chemical Assessment and Sustainability, Tongji University, Shanghai, 200092, China.

出版信息

Anal Chim Acta. 2023 Apr 29;1252:341029. doi: 10.1016/j.aca.2023.341029. Epub 2023 Mar 2.

DOI:10.1016/j.aca.2023.341029
PMID:36935145
Abstract

N-linked glycosylation (N-glycosylation) is a common protein post-translational modification, occurring on more than half of mammalian proteins; in striking contract with small molecule modifications (such as methylation, phosphorylation) with only single structures, N-glycosylation has multiple dimensional structural features (monosaccharide composition, sequence, linkage, anomer), which generates enormous N-glycan structures; and these structures widely regulate protein structure and functions. For the modification site, N-glycosylation occurs on the Asn residue among the consensus N-X-S/T/C (X≠P) motif; mutation-originated amino acid change may lead to loss of such an original motif and thus loss-of-glycosylation (LoG) or gain of such a new motif and thus gain-of-glycosylation (GoG). Both LoG and GoG generates new structures and functions of glycoproteins, which has been observed in the S protein of SARS-Cov-2 as well as malignant diseases. Here we report our glycoproteome-wide qualitative N-glycoproteomics characterization of GoGs in breast cancer Adriamycin drug resistance (ADR) cells (MCF-7/ADR) and cancer stem cells (MCF-7/ADR CSCs); comprehensive N-glycosite and N-glycan structure information at the intact N-glycopeptide level were reported.

摘要

N-连接糖基化(N-glycosylation)是一种常见的蛋白质翻译后修饰,发生在超过一半的哺乳动物蛋白上;与小分子修饰(如甲基化、磷酸化)形成鲜明对比的是,后者只有单一结构,而 N-糖基化具有多种维度的结构特征(单糖组成、序列、连接、端基异构体),从而产生了大量的 N-聚糖结构;这些结构广泛调节蛋白质的结构和功能。对于修饰位点,N-糖基化发生在共识 N-X-S/T/C(X≠P)基序中的 Asn 残基上;突变引起的氨基酸变化可能导致失去这种原始基序,从而导致糖基化缺失(LoG)或获得这种新基序,从而导致糖基化获得(GoG)。无论是 LoG 还是 GoG,都会产生糖蛋白的新结构和功能,这在 SARS-CoV-2 的 S 蛋白以及恶性疾病中都有观察到。在这里,我们报告了我们对乳腺癌阿霉素耐药(ADR)细胞(MCF-7/ADR)和癌症干细胞(MCF-7/ADR CSCs)中 GoG 的全蛋白质组定性 N-糖基蛋白质组学特征,报告了完整 N-糖肽水平的全面 N-糖基位点和 N-聚糖结构信息。

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