Baig Mohammad Hassan, Kausar Mohd Adnan, Husain Fohad Mabood, Shakil Shazi, Ahmad Irfan, Yadav Brijesh S, Saeed Mohd
Department of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Department of Biochemistry, College of Medicine, University of Hail, Saudi Arabia.
Saudi J Biol Sci. 2019 Jan;26(1):160-164. doi: 10.1016/j.sjbs.2018.08.020. Epub 2018 Aug 22.
Diabetes type 2 (T2D) is a very complex disorder with a large number of cases reported worldwide. There are several reported molecular targets which are being used towards drug design. In spite of extensive research efforts, there is no sure shot treatment available. One of the major reasons for this failure or restricted success in T2D research is the identification of a major/breakthrough therapeutic target responsible for the progression of T2D. It has been well documented that one of the major causes mediating the insulin resistance is the interaction of PLD1 with PED/PEA15. Herein, we have performed experiments to investigate the interaction between PLD1 with PED/PEA15. Furthermore, this study has explored pertinent molecular interactions involving the self-derived peptides. The peptides identified in this study are found to be capable of restricting the interaction of these two proteins. Accordingly, the study suggests that the "self-derived peptides" could be used as promising therapeutic candidate(s) against T2D.
2型糖尿病(T2D)是一种非常复杂的疾病,全球报告的病例数量众多。有几个已报道的分子靶点正被用于药物设计。尽管进行了广泛的研究,但目前尚无确切有效的治疗方法。T2D研究中这种失败或成效有限的主要原因之一是确定导致T2D进展的主要/突破性治疗靶点。有充分的文献记载,介导胰岛素抵抗的主要原因之一是PLD1与PED/PEA15的相互作用。在此,我们进行了实验以研究PLD1与PED/PEA15之间的相互作用。此外,本研究还探索了涉及自身衍生肽的相关分子相互作用。本研究中鉴定出的肽能够限制这两种蛋白质的相互作用。因此,该研究表明“自身衍生肽”有望成为对抗T2D的治疗候选物。