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抗原 MLAA-42 蛋白的同源建模和虚拟筛选研究:白血病的新药物靶点鉴定——一种方法。

Homology Modeling and Virtual Screening Studies of Antigen MLAA-42 Protein: Identification of Novel Drug Candidates against Leukemia-An Approach.

机构信息

Chemistry Department, Faculty of Science, University of Sharjah, Sharjah 27272, UAE.

Chemistry of Natural and Microbial Products Department, Pharmaceutical and Drug Industries Research Division, National Research Centre, Dokki 12622, Cairo, Egypt.

出版信息

Comput Math Methods Med. 2020 Mar 16;2020:8196147. doi: 10.1155/2020/8196147. eCollection 2020.

Abstract

Monocytic leukemia-associated antigen-42 (MLAA-42) is associated with excessive cell division and progression of leukemia. Thus, human MLAA-42 is considered as a promising target for designing of new lead molecules for leukemia treatment. Herein, the 3D model of the target was generated by homology modeling technique. The model was then evaluated using various cheminformatics servers. Moreover, the virtual screening studies were performed to explore the possible binding patterns of ligand molecules to MLAA's active site pocket. Thirteen ligand molecules from the ChemBank database were identified as they showed good binding affinities, scaffold diversity, and preferential ADME properties which may act as potent drug candidates against leukemia. The study provides the way to identify novel therapeutics with optimal efficacy, targeting MLAA-42.

摘要

单核细胞白血病相关抗原-42 (MLAA-42) 与细胞过度分裂和白血病的发展有关。因此,人类 MLAA-42 被认为是设计治疗白血病的新型先导分子的有前途的靶标。本文通过同源建模技术生成了靶标的 3D 模型。然后使用各种化学信息学服务器对模型进行了评估。此外,还进行了虚拟筛选研究,以探索配体分子与 MLAA 活性口袋的可能结合模式。从 ChemBank 数据库中鉴定出 13 种配体分子,因为它们表现出良好的结合亲和力、支架多样性和优先的 ADME 特性,可能作为针对白血病的有效候选药物。该研究为确定针对 MLAA-42 的具有最佳疗效的新型治疗药物提供了一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ca5/7102452/a369111f3b74/CMMM2020-8196147.001.jpg

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