7VQH
Solution NMR structure of Escherichia coli Total Lipid Extract Bicelle bound VR18 Antimicrobial Peptide
7VQH の概要
エントリーDOI | 10.2210/pdb7vqh/pdb |
分子名称 | VAL-ALA-ARG-GLY-TRP-GLY-ARG-LYS-CYS-PRO-LEU-PHE-GLY-LYS-ASN-LYS-SER-ARG (VR18) (1 entity in total) |
機能のキーワード | cyana 2.1, antimicrobial protein |
由来する生物種 | synthetic construct |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 2066.48 |
構造登録者 | |
主引用文献 | Mohid, S.A.,Sharma, P.,Alghalayini, A.,Saini, T.,Datta, D.,Willcox, M.D.P.,Ali, H.,Raha, S.,Singha, A.,Lee, D.,Sahoo, N.,Cranfield, C.G.,Roy, S.,Bhunia, A. A rationally designed synthetic antimicrobial peptide against Pseudomonas-associated corneal keratitis: Structure-function correlation. Biophys.Chem., 286:106802-106802, 2022 Cited by PubMed Abstract: Contact lens wearers are at an increased risk of developing Pseudomonas-associated corneal keratitis, which can lead to a host of serious ocular complications. Despite the use of topical antibiotics, ocular infections remain a major clinical problem, and a strategy to avoid Pseudomonas-associated microbial keratitis is urgently required. The hybrid peptide VR18 (VARGWGRKCPLFGKNKSR) was designed to have enhanced antimicrobial properties in the fight against Pseudomonas-induced microbial keratitis, including contact lens-related keratitis. In this paper, VR18's modes of action against Pseudomonas membranes were shown by live cell Raman spectroscopy, live cell NMR, live-cell fluorescence microscopy and measures taken using sparsely tethered bilayer lipid membrane bacterial models to be via a bacterial-specific membrane disruption mechanism. The high affinity and selectivity of the peptide were then demonstrated using in vivo, in vitro and ex vivo models of Pseudomonas infection. The extensive data presented in this work suggests that topical employment of the VR18 peptide would be a potent therapeutic agent for the prevention or remedy of Pseudomonas-associated microbial keratitis. PubMed: 35605494DOI: 10.1016/j.bpc.2022.106802 主引用文献が同じPDBエントリー |
実験手法 | SOLUTION NMR |
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