Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
School of Natural Sciences, Mathematics, and Engineering, California State University, Bakersfield, California, 93311, USA.
Protein Sci. 2023 May;32(5):e4629. doi: 10.1002/pro.4629.
Isoforms of heat shock protein 90 (HSP90) fold oncoproteins that facilitate all 10 hallmarks of cancer. However, its promise as a therapeutic target remains unfulfilled as there is still no FDA-approved drug targeting HSP90 in disease. Among the reasons hindering progress are side effects caused by pan-HSP90 inhibition. Selective targeting of the four isoforms is challenging due to high sequence and structural similarity. Surprisingly, while decades of drug discovery efforts have produced almost 400 human HSP90 structures, no single ligand has been structurally characterized across all four human isoforms to date, which could reveal structural differences to achieve selectivity. To better understand the HSP90 landscape relevant for ligand binding and design we take a three-pronged approach. First, we solved the first complete set of structures of a single ligand bound to all four human isoforms. This enabled a systematic comparison of how side-chains and water networks respond to ligand binding across isoforms. Second, we expanded our analysis to publicly available, incomplete isoform-ligand series with distinct ligand chemistry. This highlighted general trends of protein and water mobility that differ among isoforms and impact ligand binding. Third, we further probed the Hsp90α conformational landscape for accommodating a congeneric series containing the purine scaffold common to HSP90 inhibitors. This revealed how minor ligand modifications flip ligand poses and perturb water and protein conformations. Taken together, this work illustrates how a systematic approach can shed new light on an "old" target and reveal hidden isoform-specific accommodations of congeneric ligands that may be exploited in ligand discovery and design.
热休克蛋白 90(HSP90)的异构体折叠癌蛋白,促进癌症的所有 10 个特征。然而,作为治疗靶点的前景仍未实现,因为目前仍然没有 FDA 批准的针对 HSP90 的疾病治疗药物。阻碍进展的原因之一是泛 HSP90 抑制引起的副作用。由于高度的序列和结构相似性,对四个异构体的选择性靶向具有挑战性。令人惊讶的是,尽管几十年来的药物发现努力产生了近 400 个人 HSP90 结构,但迄今为止,没有一种配体在结构上被表征为所有四个人类同工型,这可能揭示结构差异以实现选择性。为了更好地理解与配体结合和设计相关的 HSP90 景观,我们采用了三管齐下的方法。首先,我们解决了第一个完整的一组结构,一个单一的配体结合到所有四个人类同工型。这使得可以系统地比较侧链和水网络如何响应配体结合的同工型。其次,我们将我们的分析扩展到具有不同配体化学的公开可用的、不完整的同工型-配体系列。这突出了在同工型之间不同的蛋白质和水流动性的一般趋势,这影响配体结合。第三,我们进一步探测了 Hsp90α 的构象景观,以适应含有 HSP90 抑制剂共同嘌呤支架的同源系列。这揭示了如何通过较小的配体修饰来翻转配体构象,并扰乱水和蛋白质构象。总之,这项工作说明了系统方法如何为“旧”目标提供新的视角,并揭示同源配体隐藏的同工型特异性适应性,这可能在配体发现和设计中得到利用。