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整合素及其配体的三维结构以及细胞黏附的构象调节。

The three-dimensional structure of integrins and their ligands, and conformational regulation of cell adhesion.

作者信息

Springer Timothy A, Wang Jia-Huai

机构信息

CBR Institute for Biomedical Research, Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Adv Protein Chem. 2004;68:29-63. doi: 10.1016/S0065-3233(04)68002-8.

Abstract

Integrins are a structurally elaborate family of adhesion molecules that transmit signals bidirectionally across the plasma membrane by undergoing large-scale structural rearrangements. By regulating cell-cell and cell-matrix contacts, integrins participate in a wide-range of biological interactions including development, tissue repair, angiogenesis, inflammation and hemostasis. From a therapeutic standpoint, integrins are probably the most important class of cell adhesion receptors. Structural investigations on integrin-ligand interactions reveal remarkable features in molecular detail. These details include the atomic basis for divalent cation-dependent ligand binding and how conformational signals are propagated long distances from one domain to another between the cytoplasm and the extracellular ligand binding site that regulate affinity for ligand, and conversely, cytosolic signaling pathways.

摘要

整合素是一类结构复杂的黏附分子家族,它们通过进行大规模的结构重排,在质膜上双向传递信号。通过调节细胞间和细胞与基质的接触,整合素参与了广泛的生物学相互作用,包括发育、组织修复、血管生成、炎症和止血。从治疗角度来看,整合素可能是最重要的一类细胞黏附受体。对整合素-配体相互作用的结构研究揭示了分子细节中的显著特征。这些细节包括二价阳离子依赖性配体结合的原子基础,以及构象信号如何从细胞质中的一个结构域远距离传播到细胞外配体结合位点的另一个结构域,从而调节对配体的亲和力,反之亦然,还有胞质信号通路。

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