Montero-Domínguez Pavel A, Mares-Sámano Sergio, Garduño-Juárez Ramón
Instituto de Ciencias Físicas, Universidad Nacional Autónoma de México, Cuernavaca, México.
CONACYT - Instituto de Ciencias Físicas, Universidad Nacional Autónoma de México, Cuernavaca, México.
J Biomol Struct Dyn. 2023 Aug-Sep;41(13):6272-6281. doi: 10.1080/07391102.2022.2106514. Epub 2022 Aug 2.
Discrepin is a 38-residue α-toxin extracted from the venom of the Venezuelan scorpion , which inhibits ionic transit in the voltage-dependent potassium channels (Kv) of A-type current. The effect of specific residues on the IC between Discrepine and Kv4.3, the main component of A-type currents, is known; however, the molecular details of the toxin-channel interaction are not known. In this work, we present interaction models between Discrepin (wt) and two peptide variants (V6K/D20K and K13A) on the pore-forming domain of the Kv4.3 channel obtained from homology, docking, and molecular dynamics modeling techniques. The free energy calculations in these models correspond to the order of the experimentally determined IC values. Our studies shed light on the role of the K13 residue as responsible for occluding the Kv4.3 selectivity filter and the importance of the V6K mutation in the approach and stabilization of toxin-channel complex interactions.Communicated by Ramaswamy H. Sarma.
Discrepin是一种从委内瑞拉蝎子毒液中提取的由38个氨基酸残基组成的α毒素,它能抑制A型电流的电压依赖性钾通道(Kv)中的离子转运。已知特定残基对Discrepin与A型电流的主要成分Kv4.3之间的半数抑制浓度(IC)的影响;然而,毒素-通道相互作用的分子细节尚不清楚。在这项工作中,我们展示了通过同源性、对接和分子动力学建模技术获得的Discrepin(野生型)与Kv4.3通道孔形成结构域上的两个肽变体(V6K/D20K和K13A)之间的相互作用模型。这些模型中的自由能计算与实验测定的IC值顺序一致。我们的研究揭示了K13残基在封闭Kv4.3选择性过滤器中的作用以及V6K突变在毒素-通道复合物相互作用的接近和稳定中的重要性。由Ramaswamy H. Sarma传达。