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荧光小分子探针调节和探索 α2β1 整合素功能。

Fluorescent small molecule probe to modulate and explore α2β1 integrin function.

机构信息

Computational Bioscience Laboratory, Department of Biological and Environmental Science, University of Jyväskylä, Finland.

出版信息

J Am Chem Soc. 2011 Sep 21;133(37):14558-61. doi: 10.1021/ja206086c. Epub 2011 Aug 30.

Abstract

Collagen binding integrins are an important family of cell surface receptors that mediate bidirectionally signals between the interior of the cell and the extracellular matrix. The protein-protein interactions between cells and collagen are necessary for many physiological functions, but also promote diseases. For example, the interaction of α2β1 integrin and collagen has been shown to have an important role in thrombus formation and cancer spread. The fact that the discovery of small molecules that can block such protein-protein interactions is highly challenging has significantly hindered the discovery of pharmaceutical agents to treat these diseases. Here, we present a rationally designed novel fluorescent molecule that can be synthesized in just a few minutes from commercially available starting materials. This molecule blocks the protein-protein interaction between α2β1 integrin and collagen, and due to its fluorescent properties, it can be employed in wide variety of biological applications.

摘要

胶原结合整合素是细胞表面受体的一个重要家族,介导细胞内部与细胞外基质之间的双向信号。细胞与胶原之间的蛋白-蛋白相互作用对于许多生理功能是必要的,但也促进了疾病的发生。例如,α2β1 整合素与胶原的相互作用已被证明在血栓形成和癌症扩散中具有重要作用。能够阻断这种蛋白-蛋白相互作用的小分子的发现极具挑战性,这极大地阻碍了治疗这些疾病的药物的发现。在这里,我们提出了一种合理设计的新型荧光分子,它可以从商业上可获得的起始原料在短短几分钟内合成。该分子阻断了α2β1 整合素与胶原之间的蛋白-蛋白相互作用,并且由于其荧光特性,可以应用于广泛的生物应用中。

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