Schubert W D, Göbel G, Diepholz M, Darji A, Kloer D, Hain T, Chakraborty T, Wehland J, Domann E, Heinz D W
Department of Structural Biology, German Research Center for Biotechnology, Braunschweig.
J Mol Biol. 2001 Sep 28;312(4):783-94. doi: 10.1006/jmbi.2001.4989.
Listeria monocytogenes is an opportunistic, food-borne human and animal pathogen. Host cell invasion requires the action of the internalins A (InlA) and B (InlB), which are members of a family of listerial cell-surface proteins. Common to these proteins are three distinctive N-terminal domains that have been shown to direct host cell-specific invasion for InlA and InlB. Here, we present the high-resolution crystal structures of these domains present in InlB and InlH, and show that they constitute a single "internalin domain". In this internalin domain, a central LRR region is flanked contiguously by a truncated EF-hand-like cap and an immunoglobulin (Ig)-like fold. The extended beta-sheet, resulting from the distinctive fusion of the LRR and the Ig-like folds, constitutes an adaptable concave interaction surface, which we propose is responsible for the specific recognition of the host cellular binding partners during infection.
单核细胞增生李斯特菌是一种机会性食源性病原体,可感染人类和动物。宿主细胞入侵需要内化素A(InlA)和内化素B(InlB)发挥作用,它们是李斯特菌细胞表面蛋白家族的成员。这些蛋白的共同特征是具有三个独特的N端结构域,已证明这些结构域可指导InlA和InlB对宿主细胞的特异性入侵。在此,我们展示了InlB和InlH中这些结构域的高分辨率晶体结构,并表明它们构成了一个单一的“内化素结构域”。在这个内化素结构域中,一个中央亮氨酸丰富重复序列(LRR)区域连续两侧分别是一个截短的类EF手型帽和一个免疫球蛋白(Ig)样折叠。由LRR和Ig样折叠的独特融合产生的延伸β片层构成了一个适应性凹面相互作用表面,我们认为该表面负责感染期间对宿主细胞结合伴侣的特异性识别。