Discipline of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, University of Science, Malaysia (USM), 11800, Penang, Malaysia.
College of Pharmacy, University of Uruk, Baghdad, Iraq.
Arch Razi Inst. 2022 Apr 30;77(2):843-852. doi: 10.22092/ARI.2022.357124.1980. eCollection 2022 Apr.
Nowadays dengue virus infection (DENV) is one of the major health complications in the world. Although DENV is an old and common disease, unfortunately, until now, there are no specific relevant treatments available for it. This study, therefore, aimed to design, as well as synthesize selective peptide inhibitors, and investigate their activity by NS2B/NS3 protease inhibition assay. The design of the peptide ligands was based on studying the interactions with the dengue NS2B/NS3 protease using the computational docking technique in the MOE and AutoDock (version 4.2) software. To this end, the researchers designed 26 linear pentapeptides based on previous studies. It was revealed that two linear pentapeptides (i.e., GKRRK and KRRRK) are the best potential inhibitors. Furthermore, based on the findings of the two independent docking programs, the peptide GKRRK was synthesized by solid-phase peptide synthesis and its structure was confirmed. The protease inhibitor study was conducted for these two peptides to examine their activity against the dengue virus using a protin in as a control. It was found that the designed potential peptides possess interesting inhibition against the NS2B/NS3 protease. Additionally, the findings showed that the peptide GKRRK had the highest percentage of inhibition (71.11%) at 100 µM with the IC of 48.87 µM; therefore, this linear peptide could serve as a good inhibitor for the DENV.
如今,登革热病毒感染(DENV)是世界上主要的健康并发症之一。尽管 DENV 是一种古老而常见的疾病,但不幸的是,直到现在,还没有针对它的特定治疗方法。因此,本研究旨在设计和合成选择性肽抑制剂,并通过 NS2B/NS3 蛋白酶抑制试验来研究它们的活性。肽配体的设计是基于使用 MOE 和 AutoDock(版本 4.2)软件中的计算对接技术研究与登革热 NS2B/NS3 蛋白酶的相互作用。为此,研究人员根据先前的研究设计了 26 条线性五肽。结果表明,两条线性五肽(即 GKRRK 和 KRRRK)是最有潜力的抑制剂。此外,基于两个独立对接程序的结果,通过固相肽合成合成了肽 GKRRK,并对其结构进行了确认。为了研究这些两种肽对登革热病毒的活性,以蛋白作为对照进行了蛋白酶抑制剂研究。结果发现,设计的潜在肽对 NS2B/NS3 蛋白酶具有有趣的抑制作用。此外,研究结果表明,肽 GKRRK 在 100 µM 时具有最高的抑制百分比(71.11%),IC 为 48.87 µM;因此,这种线性肽可以作为 DENV 的良好抑制剂。