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对反刍动物 Toll 样受体 1-10 的亮氨酸丰富重复序列进行同源建模和结构比较。

Homology modeling and structural comparison of leucine rich repeats of Toll like receptors 1-10 of ruminants.

机构信息

Department of Animal Biotechnology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, 600 007, Chennai, India.

出版信息

J Mol Model. 2013 Sep;19(9):3863-74. doi: 10.1007/s00894-013-1871-3. Epub 2013 Jun 28.

Abstract

Toll-like receptors (TLRs) are transmembrane receptors composed of extra cellular leucine rich repeats (LRRs) that identify specific pathogen associated molecular patterns triggering a innate immune cascade. The LRR regions of TLR 1-10 proteins of goat (Capra hircus), sheep (Ovis aries), buffalo (Bubalus bubalis) and bovine (Bos taurus) were modeled using MODELLER 9v7 tool and validated. The similarities and variations of these 10 TLRs extracellular regions of each species were compared using online servers like FATCAT, SSM and SSAP. It was evident that the LRRs of TLRs like 1, 2, 3 and 6 showed structural convergence with <1 % RMSD deviation while TLRs like 5, 7, 8 and 9 had high divergence. Docking analysis showed that TLR 2, 3 and 7 of all the selected four ruminant species were able to bind with their corresponding ligands like Peptidoglycan (PGN), Poly I:C, Resiquimod (R-848) and Imiquimod. However, there were variations in the active site regions, interacting residues and the number of bonded interactions. Variations seen among TLR structures and their ligand binding characteristics is likely to be responsible for species and breed specific genetic resistance observed among species or breeds.

摘要

Toll 样受体 (TLRs) 是一种跨膜受体,由识别特定病原体相关分子模式触发先天免疫级联反应的细胞外富含亮氨酸重复序列 (LRRs) 组成。使用 MODELER 9v7 工具对山羊 (Capra hircus)、绵羊 (Ovis aries)、水牛 (Bubalus bubalis) 和牛 (Bos taurus) 的 TLR1-10 蛋白的 LRR 区域进行建模,并进行了验证。使用在线服务器(如 FATCAT、SSM 和 SSAP)比较了这 10 种 TLR 种属外区域的相似性和差异。结果表明,TLR1、2、3 和 6 的 LRR 与 <1% RMSD 偏差表现出结构收敛,而 TLR5、7、8 和 9 则高度发散。对接分析表明,所选的 4 种反刍动物的 TLR2、3 和 7 均能够与相应的配体(如肽聚糖 (PGN)、聚肌苷酸:聚胞苷酸 (Poly I:C)、瑞喹莫德 (R-848) 和咪喹莫特)结合。然而,在活性位点区域、相互作用的残基和键合相互作用的数量上存在差异。TLR 结构及其配体结合特性的差异可能是导致种间或品种间观察到的种特异性和品种特异性遗传抗性的原因。

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