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Adhesion protein networks reveal functions proximal and distal to cell-matrix contacts

机译:粘附蛋白网络揭示细胞基质接触近端和远端的功能

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摘要

Cell adhesion to the extracellular matrix is generally mediated by integrin receptors, which bind to intracellular adhesion proteins that form multi-molecular scaffolding and signalling complexes. The networks of proteins, and their interactions, are dynamic, mechanosensitive and extremely complex. Recent efforts to characterise adhesions using a variety of technologies, including imaging, proteomics and bioinformatics, have provided new insights into their composition, organisation and how they are regulated, and have also begun to reveal unexpected roles for so-called adhesion proteins in other cellular compartments (for example, the nucleus or centrosomes) in diseases such as cancer. We believe this is opening a new chapter on understanding the wider functions of adhesion proteins, both proximal and distal to cell-matrix contacts.
机译:细胞对细胞外基质的粘附通常由整联蛋白受体介导,整联蛋白受体与形成多分子支架和信号复合物的细胞内粘附蛋白结合。蛋白质网络及其相互作用是动态的,机械敏感的并且极其复杂。最近使用成像,蛋白质组学和生物信息学等多种技术表征黏附的努力,为它们的组成,组织以及如何调控提供了新见解,并且也开始揭示所谓黏附蛋白在其他细胞中的意想不到的作用诸如癌症之类的疾病中的细胞室(例如,核或中心体)。我们相信这为了解细胞基质接触的近端和远端的粘附蛋白的更广泛功能开辟了新篇章。

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