Ewert Wiebke, Günther Sebastian, Miglioli Francesca, Falke Sven, Reinke Patrick Y A, Niebling Stephan, Günther Christian, Han Huijong, Srinivasan Vasundara, Brognaro Hévila, Lieske Julia, Lorenzen Kristina, Garcia-Alai Maria M, Betzel Christian, Carcelli Mauro, Hinrichs Winfried, Rogolino Dominga, Meents Alke
Center for Free-Electron Laser Science CFEL, Deutsches Elektronen-Synchrotron DESY, Hamburg, Germany.
Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Front Chem. 2022 Apr 11;10:832431. doi: 10.3389/fchem.2022.832431. eCollection 2022.
The papain-like protease (PLpro) of SARS-CoV-2 is essential for viral propagation and, additionally, dysregulation of the host innate immune system. Using a library of 40 potential metal-chelating compounds we performed an X-ray crystallographic screening against PLpro. As outcome we identified six compounds binding to the target protein. Here we describe the interaction of one hydrazone (H1) and five thiosemicarbazone (T1-T5) compounds with the two distinct natural substrate binding sites of PLpro for ubiquitin and ISG15. H1 binds to a polar groove at the S1 binding site by forming several hydrogen bonds with PLpro. T1-T5 bind into a deep pocket close to the polyubiquitin and ISG15 binding site S2. Their interactions are mainly mediated by multiple hydrogen bonds and further hydrophobic interactions. In particular compound H1 interferes with natural substrate binding by sterical hindrance and induces conformational changes in protein residues involved in substrate binding, while compounds T1-T5 could have a more indirect effect. Fluorescence based enzyme activity assay and complementary thermal stability analysis reveal only weak inhibition properties in the high micromolar range thereby indicating the need for compound optimization. Nevertheless, the unique binding properties involving strong hydrogen bonding and the various options for structural optimization make the compounds ideal lead structures. In combination with the inexpensive and undemanding synthesis, the reported hydrazone and thiosemicarbazones represent an attractive scaffold for further structure-based development of novel PLpro inhibitors by interrupting protein-protein interactions at the S1 and S2 site.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的木瓜蛋白酶样蛋白酶(PLpro)对病毒传播至关重要,此外,它还会导致宿主先天免疫系统失调。我们使用包含40种潜在金属螯合化合物的文库,对PLpro进行了X射线晶体学筛选。结果,我们鉴定出六种与目标蛋白结合的化合物。在此,我们描述了一种腙(H1)和五种硫代氨基脲(T1-T5)化合物与PLpro用于泛素和ISG15的两个不同天然底物结合位点的相互作用。H1通过与PLpro形成多个氢键,结合到S1结合位点的一个极性凹槽中。T1-T5结合到靠近多聚泛素和ISG15结合位点S2的一个深口袋中。它们的相互作用主要由多个氢键和进一步的疏水相互作用介导。特别是化合物H1通过空间位阻干扰天然底物结合,并诱导参与底物结合的蛋白质残基发生构象变化,而化合物T1-T5可能具有更间接的作用。基于荧光的酶活性测定和互补热稳定性分析表明,在高微摩尔范围内只有微弱的抑制特性,从而表明需要对化合物进行优化。然而,涉及强氢键的独特结合特性和各种结构优化选项使这些化合物成为理想的先导结构。结合廉价且要求不高的合成方法,所报道的腙和硫代氨基脲代表了一种有吸引力的支架,可通过中断S1和S2位点的蛋白质-蛋白质相互作用,进一步基于结构开发新型PLpro抑制剂。