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基于计算机模拟的方法鉴定和评价中药天然化合物作为潜在的肌肉生长抑制素抑制剂。

Identification and Evaluation of Traditional Chinese Medicine Natural Compounds as Potential Myostatin Inhibitors: An In Silico Approach.

机构信息

Department of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.

Research Institute of Cell Culture, Yeungnam University, Gyeongsan 38541, Korea.

出版信息

Molecules. 2022 Jul 4;27(13):4303. doi: 10.3390/molecules27134303.

Abstract

Myostatin (MSTN), a negative regulator of muscle mass, is reported to be increased in conditions linked with muscle atrophy, sarcopenia, and other muscle-related diseases. Most pharmacologic approaches that treat muscle disorders are ineffective, emphasizing the emergence of MSTN inhibition. In this study, we used computational screening to uncover natural small bioactive inhibitors from the Traditional Chinese Medicine database (~38,000 compounds) for the MSTN protein. Potential ligands were screened, based on binding affinity (150), physicochemical (53) and ADMET properties (17). We found two hits (ZINC85592908 and ZINC85511481) with high binding affinity and specificity, and their binding patterns with MSTN protein. In addition, molecular dynamic simulations were run on each complex to better understand the interaction mechanism of MSTN with the control (curcumin) and the hit compounds (ZINC85592908 and ZINC85511481). We determined that the hits bind to the active pocket site (Helix region) and trigger conformational changes in the MSTN protein. Since the stability of the ZINC85592908 compound was greater than the MSTN control, we believe that ZINC85592908 has therapeutic potential against the MSTN protein and may hinder downstream singling by inhibiting the MSTN protein and increasing myogenesis in the skeletal muscle tissues.

摘要

肌肉生长抑制素 (MSTN) 是肌肉质量的负调控因子,据报道,在与肌肉萎缩、肌肉减少症和其他肌肉相关疾病相关的情况下,其水平会升高。大多数治疗肌肉疾病的药物方法都无效,这强调了 MSTN 抑制的出现。在这项研究中,我们使用计算筛选从中药数据库 (~38000 种化合物) 中发现针对 MSTN 蛋白的天然小分子生物活性抑制剂。根据结合亲和力 (150)、物理化学性质 (53) 和 ADMET 特性 (17),筛选潜在的配体。我们发现了两个具有高结合亲和力和特异性的命中物 (ZINC85592908 和 ZINC85511481),以及它们与 MSTN 蛋白的结合模式。此外,对每个复合物进行了分子动力学模拟,以更好地理解 MSTN 与对照 (姜黄素) 和命中化合物 (ZINC85592908 和 ZINC85511481) 的相互作用机制。我们确定命中物结合到活性口袋部位 (螺旋区) 并引发 MSTN 蛋白的构象变化。由于 ZINC85592908 化合物的稳定性大于 MSTN 对照,我们认为 ZINC85592908 对 MSTN 蛋白具有治疗潜力,并且可能通过抑制 MSTN 蛋白和增加骨骼肌组织中的成肌作用来阻碍下游信号传导。

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