Dadgar Saedeh, Floriano Wely B
Department of Chemistry at Lakehead University and Thunder Bay Regional Research Institute, Thunder Bay, ON P7B 5E1, Canada.
Department of Chemistry at Lakehead University and Thunder Bay Regional Research Institute, Thunder Bay, ON P7B 5E1, Canada.
Mol Cell Probes. 2015 Jun;29(3):135-43. doi: 10.1016/j.mcp.2015.02.002. Epub 2015 Mar 4.
The development of molecular probes targeting proteins has traditionally relied on labeling compounds already known to bind to the protein of interest. These known ligands bind to orthosteric or allosteric sites in their target protein as a way to control their activity. Binding pockets other than known orthosteric or allosteric sites may exist that are large enough to accommodate a ligand without significantly disrupting protein activity. Such sites may provide opportunities to discriminate between subtypes or other closely related proteins, since they are under less evolutionary pressure to be conserved. The Protein Scanning with Virtual Ligand Screening (PSVLS) approach was previously used to identify a novel inhibitor and a fluorescent probe against the catalytic site of the botulinum neurotoxin subtype A (BoNT/A). PSVLS screens compound databases against multiple sites within a target protein, and the results for all the sites probed against BoNT/A, not only the catalytic site, are available online. Here, we analyze the PSVLS data for multiple sites in order to identify molecular probes with affinity for binding pockets other than the catalytic site of BoNT/A. BoNT/A is a large protein with a light (LC) and a heavy (HC) chain that can be assayed separately. We used scintillation proximity assay (SPA) to test experimentally 5 probe candidates predicted computationally to have affinity for different non-orthosteric binding regions within the HC and LC, and one compound predicted not to have affinity for either domain. The binding profiles obtained experimentally confirmed the targeting of multiple and spatially distinct pockets within BoNT/A. Moreover, inhibition assay results indicate that some of these probes do not significantly interfere with the catalytic activity of BoNT/A.
传统上,针对蛋白质的分子探针开发依赖于标记已知能与目标蛋白质结合的化合物。这些已知配体与目标蛋白质中的正构或变构位点结合,以此来控制其活性。除了已知的正构或变构位点外,可能还存在其他结合口袋,其大小足以容纳一个配体而不会显著破坏蛋白质活性。由于这些位点在进化过程中受到的保守压力较小,它们可能为区分亚型或其他密切相关的蛋白质提供机会。蛋白质虚拟配体筛选扫描(PSVLS)方法先前被用于鉴定一种针对肉毒杆菌神经毒素A亚型(BoNT/A)催化位点的新型抑制剂和荧光探针。PSVLS针对目标蛋白质内的多个位点筛选化合物数据库,并且针对BoNT/A探测的所有位点(不仅是催化位点)的结果均可在线获取。在此,我们分析多个位点的PSVLS数据,以鉴定对BoNT/A催化位点以外的结合口袋具有亲和力的分子探针。BoNT/A是一种由轻链(LC)和重链(HC)组成的大蛋白,可分别进行检测。我们使用闪烁邻近分析(SPA)对通过计算预测对HC和LC内不同非正构结合区域具有亲和力的5种探针候选物以及一种预测对两个结构域均无亲和力的化合物进行了实验测试。实验获得的结合图谱证实了BoNT/A内多个且空间上不同的口袋被靶向。此外,抑制分析结果表明,其中一些探针不会显著干扰BoNT/A 的催化活性。