Schwarz-Linek Ulrich, Höök Magnus, Potts Jennifer R
Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Mol Microbiol. 2004 May;52(3):631-41. doi: 10.1111/j.1365-2958.2004.04027.x.
Many pathogenic Gram-positive bacteria produce cell wall-anchored proteins that bind to components of the extracellular matrix (ECM) of the host. These bacterial MSCRAMMs (microbial surface components recognizing adhesive matrix molecules) are thought to play a critical role in infection. One group of MSCRAMMs, produced by staphylococci and streptococci, targets fibronectin (Fn, a glycoprotein found in the ECM and body fluids of vertebrates) using repeats in the C-terminal region of the bacterial protein. These bacterial Fn-binding proteins (FnBPs) mediate adhesion to host tissue and bacterial uptake into non-phagocytic host cells. Recent studies on interactions between the host and bacterial proteins at the residue-specific level and on the mechanism of host cell invasion are providing a much clearer picture of these processes.
许多致病性革兰氏阳性菌会产生细胞壁锚定蛋白,这些蛋白可与宿主细胞外基质(ECM)的成分结合。这些细菌的微生物表面成分识别黏附基质分子(MSCRAMMs)被认为在感染过程中起关键作用。葡萄球菌和链球菌产生的一组MSCRAMMs利用细菌蛋白C端区域的重复序列靶向纤连蛋白(Fn,一种存在于脊椎动物ECM和体液中的糖蛋白)。这些细菌纤连蛋白结合蛋白(FnBPs)介导细菌与宿主组织的黏附以及细菌被非吞噬性宿主细胞摄取。最近在残基特异性水平上对宿主与细菌蛋白之间相互作用以及宿主细胞入侵机制的研究,正使人们对这些过程有更清晰的认识。