Departamento de Química Física, Universidad de Valencia, 46100, Burjassot, Spain.
Angew Chem Int Ed Engl. 2021 Dec 1;60(49):25933-25941. doi: 10.1002/anie.202110027. Epub 2021 Nov 3.
We present the results of classical and QM/MM simulations for the inhibition of SARS-CoV-2 3CL protease by a hydroxymethylketone inhibitor, PF-00835231. In the noncovalent complex the carbonyl oxygen atom of the warhead is placed in the oxyanion hole formed by residues 143 to 145, while P1-P3 groups are accommodated in the active site with interactions similar to those observed for the peptide substrate. According to alchemical free energy calculations, the P1' hydroxymethyl group also contributes to the binding free energy. Covalent inhibition of the enzyme is triggered by the proton transfer from Cys145 to His41. This step is followed by the nucleophilic attack of the Sγ atom on the carbonyl carbon atom of the inhibitor and a proton transfer from His41 to the carbonyl oxygen atom mediated by the P1' hydroxyl group. Computational simulations show that the addition of a chloromethyl substituent to the P1' group may lower the activation free energy for covalent inhibition.
我们展示了通过羟甲基酮抑制剂 PF-00835231 抑制 SARS-CoV-2 3CL 蛋白酶的经典和QM/MM 模拟的结果。在非共价复合物中,弹头的羰基氧原子位于由残基 143 到 145 形成的氧阴离子穴中,而 P1-P3 基团则与肽底物观察到的相互作用相似,被容纳在活性位点中。根据变分自由能计算,P1' 羟甲基基团也有助于结合自由能。酶的共价抑制是由 Cys145 向 His41 的质子转移引发的。接下来是 Sγ 原子对抑制剂羰基碳原子的亲核攻击,以及 His41 通过 P1' 羟基向羰基氧原子的质子转移。计算模拟表明,在 P1' 基团上添加氯甲基取代基可能会降低共价抑制的活化自由能。