Jois Seetharama D S, Nagarajarao Latha M, Prabhakaran M, Balasubramaniam A
Department of Pharmacy, National University of Singapore, Singapore 117543.
J Biomol Struct Dyn. 2006 Apr;23(5):497-508.
Neuropeptide Y (NPY), receptors belong to the G-protein coupled receptor superfamily. NPY mediates several physiological responses, such as blood pressure, food intake, sedation. These actions of NPY are mediated by six receptor subtypes denoted as Y1-Y5 and y6. Modeling of receptor subtypes and binding site identification is an important step in developing new therapeutic agents. We have attempted to model the three NPY receptor types, Y1, Y4, and Y5 using homology modeling and threading methods. The models are consistent with previously reported experimental evidence. To understand the interaction and selectivity of NPY analogues with different neuropeptide receptors, docking studies of two neuropeptide analogues (BVD10 and BVD15) with receptors Y1 and Y4 were carried out. Results of the docking studies indicated that the interaction of ligands BVD10 and BVD15 with Y1 and Y4 receptors are different. These results were evaluated for selectivity of peptide analogues BVD10 and BVD15 towards the receptors.
神经肽Y(NPY)受体属于G蛋白偶联受体超家族。NPY介导多种生理反应,如血压、食物摄入、镇静。NPY的这些作用由六种受体亚型介导,分别称为Y1 - Y5和y6。受体亚型建模和结合位点识别是开发新治疗药物的重要步骤。我们试图使用同源建模和穿线法对三种NPY受体类型Y1、Y4和Y5进行建模。这些模型与先前报道的实验证据一致。为了理解NPY类似物与不同神经肽受体的相互作用和选择性,对两种神经肽类似物(BVD10和BVD15)与Y1和Y4受体进行了对接研究。对接研究结果表明,配体BVD10和BVD15与Y1和Y4受体的相互作用不同。对这些结果进行了评估,以确定肽类似物BVD10和BVD15对受体的选择性。