Tuckwell D S, Humphries M J
Wellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, University of Manchester, UK.
FEBS Lett. 1997 Jan 6;400(3):297-303. doi: 10.1016/s0014-5793(96)01368-3.
The integrins are a family of cell surface receptors that mediate biologically important adhesive interactions. Integrin-ligand binding has been extensively studied because of the potential for the development of anti-adhesive therapies, but the molecular basis of this interaction is still poorly understood. A conserved region near the N-terminus of the beta subunit appears to be of particular importance in ligand binding, but to date this domain has not been expressed in isolation. As a prelude to expression and potential structure determination, we have performed a detailed structure prediction for this region. Primary, secondary and tertiary structure analyses indicate that the region folds into a von Willebrand factor A-domain, thereby potentially placing a previously characterised module at the centre of a key functional region.
整合素是一类细胞表面受体,介导具有生物学重要性的黏附相互作用。由于抗黏附疗法的发展潜力,整合素-配体结合已得到广泛研究,但这种相互作用的分子基础仍知之甚少。β亚基N端附近的一个保守区域在配体结合中似乎特别重要,但迄今为止该结构域尚未单独表达。作为表达和潜在结构测定的前奏,我们对该区域进行了详细的结构预测。一级、二级和三级结构分析表明,该区域折叠成一个血管性血友病因子A结构域,从而可能将一个先前已表征的模块置于关键功能区域的中心。