Novartis Vaccines, Via Fiorentina 1, 53100 Siena, Italy.
Mol Cell Proteomics. 2012 Apr;11(4):M111.015206. doi: 10.1074/mcp.M111.015206. Epub 2011 Dec 22.
Very few studies have so far been dedicated to the systematic analysis of protein interactions occurring between surface and/or secreted proteins in bacteria. Such interactions are expected to play pivotal biological roles that deserve investigation. Taking advantage of the availability of a detailed map of surface and secreted proteins in Streptococcus pyogenes (group A Streptococcus (GAS)), we used protein array technology to define the "surface interactome" in this important human pathogen. Eighty-three proteins were spotted on glass slides in high density format, and each of the spotted proteins was probed for its capacity to interact with any of the immobilized proteins. A total of 146 interactions were identified, 25 of which classified as "reciprocal," namely, interactions that occur irrespective of which of the two partners was immobilized on the chip or in solution. Several of these interactions were validated by surface plasmon resonance and supported by confocal microscopy analysis of whole bacterial cells. By this approach, a number of interesting interactions have been discovered, including those occurring between OppA, DppA, PrsA, and TlpA, proteins known to be involved in protein folding and transport. These proteins, all localizing at the septum, might be part, together with HtrA, of the recently described ExPortal complex of GAS. Furthermore, SpeI was found to strongly interact with the metal transporters AdcA and Lmb. Because SpeI strictly requires zinc to exert its function, this finding provides evidence on how this superantigen, a major player in GAS pathogenesis, can acquire the metal in the host environment, where it is largely sequestered by carrier proteins. We believe that the approach proposed herein can lead to a deeper knowledge of the mechanisms underlying bacterial invasion, colonization, and pathogenesis.
迄今为止,很少有研究致力于系统分析细菌表面和/或分泌蛋白之间发生的蛋白质相互作用。这些相互作用预计将发挥关键的生物学作用,值得研究。利用 A 组链球菌(GAS)表面和分泌蛋白详细图谱的可用性,我们使用蛋白质芯片技术来定义这种重要的人类病原体中的“表面相互作用组”。83 种蛋白质以高密度格式点样在玻璃幻灯片上,并用固定化蛋白质探测每种点样蛋白质与任何固定化蛋白质的相互作用能力。总共鉴定出 146 种相互作用,其中 25 种被归类为“相互”,即无论固定在芯片上或溶液中的是哪两个伙伴,都会发生相互作用。这些相互作用中的几个通过表面等离子体共振得到了验证,并通过全细菌细胞的共聚焦显微镜分析得到了支持。通过这种方法,发现了许多有趣的相互作用,包括 OppA、DppA、PrsA 和 TlpA 之间的相互作用,这些蛋白质已知参与蛋白质折叠和运输。这些定位于隔膜的蛋白质可能与 HtrA 一起,成为最近描述的 GAS 外门复合物的一部分。此外,SpeI 被发现与金属转运蛋白 AdcA 和 Lmb 强烈相互作用。由于 SpeI 严格需要锌才能发挥其功能,这一发现为这种超级抗原(GAS 发病机制中的主要参与者)如何在宿主环境中获取金属提供了证据,在宿主环境中,金属主要被载体蛋白隔离。我们相信,本文提出的方法可以深入了解细菌侵袭、定植和发病机制的机制。