Ponnuraj K, Jedrzejas M J
Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
J Mol Biol. 2000 Jun 16;299(4):885-95. doi: 10.1006/jmbi.2000.3817.
Hyaluronic acid (HA) is an important constituent of the extracellular matrix; its bacterial degradation has been postulated to contribute to the spread of certain streptococci through tissue. Pneumococci and other streptococci produce hyaluronate lyase, an enzyme which depolymerizes HA, thus hyaluronate lyase might contribute directly to bacterial invasion. Although two different mechanisms for lyase action have been proposed, there was no crystallographic evidence to support those mechanisms. Here, we report the high-resolution crystal structure of Streptococcus pneumoniae hyaluronate lyase in the presence of HA disaccharide product, which ultimately provides the first crystallographic evidence for the binding of HA to hyaluronate lyase. This structural complex revealed a key interaction between the Streptococcus peneumoniae hyaluronate lyase protein and the product, and supports our previously proposed novel catalytic mechanism for HA degradation based on the native Streptococcus peneumoniae hyaluronate lyase structure. The information provided by this complex structure will likely be useful in the development of antimicrobial pharmaceutical agents.
透明质酸(HA)是细胞外基质的重要组成部分;据推测,其细菌降解有助于某些链球菌在组织中扩散。肺炎球菌和其他链球菌会产生透明质酸裂解酶,这种酶能使HA解聚,因此透明质酸裂解酶可能直接促成细菌入侵。尽管已经提出了两种不同的裂解酶作用机制,但尚无晶体学证据支持这些机制。在此,我们报道了在存在HA二糖产物的情况下肺炎链球菌透明质酸裂解酶的高分辨率晶体结构,这最终为HA与透明质酸裂解酶的结合提供了首个晶体学证据。这种结构复合物揭示了肺炎链球菌透明质酸裂解酶蛋白与产物之间的关键相互作用,并支持了我们先前基于天然肺炎链球菌透明质酸裂解酶结构提出的HA降解新催化机制。这种复合物结构提供的信息可能对抗菌药物制剂的开发有用。