基于嗜冷假单胞菌群体感应系统LuxR蛋白筛选靶向肽及抑制生物被膜形成OA
Screening of LuxR-targeted peptides in the quorum sensing system of Pseudomonas psychrophila and their inhibition of biofilm formation
[目的]细菌形成生物被膜与群体感应系统(QS)调控有关,本研究基于冷藏鱿鱼嗜冷假单胞菌 QS 系统 LuxR 蛋白筛选靶向肽,研究其抑制生物被膜形成能力.[方法]以黄鲫蛋白肽和凡纳对虾 Pelle 蛋白肽段为肽源筛选备用肽,采用分子对接技术分别考察 N-酰基高丝氨酸内酯(AHL)型信号分子和备用肽与嗜冷假单胞菌 LuxR 蛋白对接情况,选择对接效果优于信号分子的备用肽为目标肽,定点替换目标肽氨基酸设计系列衍生肽,考察衍生肽与 LuxR 蛋白对接能力,筛选适宜衍生肽为 LuxR 蛋白靶向肽,检验目标肽和靶向肽抑制生物被膜形成能力.[结果]筛选出 5 条备用肽 AAVVFMLR、PGK、FWAKSQL、MANRVGF 和HLRVGW,只有PGK 能与6 个LuxR 蛋白成功对接,且与LuxR 蛋白SSOs_2029对接结合能(-447.26 kcal/mol)远低于 AHL 型信号分子的结合能.但目标肽 PGK 无法与LuxR 蛋白 SSOs_1080 成功对接,经氨基酸定点替换得到能与 SSOs_1080 对接成功的靶向肽 KGG 和 RGG,且对接结合能低于绝大多数信号分子.目标肽 PGK、靶向肽 KGG 和RGG 对嗜冷假单胞菌最小抑菌浓度(MIC)为 4 mg/mL,最小杀菌浓度为 8 mg/mL.在 1/2 MIC 不影响菌体正常生长下,RGG 对生物被膜形成抑制率显著高于PGK 和KGG(P<0.05).[结论]靶向肽 RGG 竞争 AHL 信号分子与嗜冷假单胞菌 LuxR 蛋白结合,对生物被膜形成有抑制作用.为快速筛选嗜冷假单胞菌肽类群体感应抑制剂研究奠定理论基础.
Bacterial biofilm formation is closely regulated by quorum sensing(QS).This study screened peptides targeting the LuxR protein of the QS system in Pseudomonas psychrophila isolated from refrigerated squid,and investigated their inhibitory effects on biofilm formation.Candidate peptides were selected from half-fin anchovy(Setipinna taty)protein hydrolysate and Pacific white shrimp(Penaeus vannamei)Pelle protein-derived peptides.Molecular docking was employed to comparatively evaluate the binding interactions of N-acyl homoserine lactone(AHL)signal molecules and candidate peptides with the LuxR protein of P.psychrophila.Peptides exhibiting superior binding affinity relative to AHLs were selected as target peptides,and a series of derivative peptides were rationally designed through site-directed amino acid substitution.The docking capacities of derivative peptides against LuxR proteins were evaluated.Derivatives with optimal LuxR-binding capacity were identified as targeted peptides,and the biofilm inhibition efficacy of both target and targeted peptides was subsequently assessed.Results showed that five candidate peptides(AAVVFMLR,PGK,FWAKSQL,MANRVGF,and HLRVGW)were screened.Only PGK successfully docked with six LuxR proteins,exhibiting a binding energy of-447.26 kcal/mol with the LuxR protein SSOs_2029,markedly lower than that of AHL-type signal molecules.However,PGK failed to dock with SSOs_1080.Through site-directed amino acid substitution,targeted peptides KGG and RGG were yielded,which successfully docked with SSOs_1080 with binding energies lower than most endogenous signal molecules.The minimum inhibitory concentration(MIC)and minimum bactericidal concentration of target peptide PGK and targeted peptides KGG and RGG against P.psychrophila were 4 and 8 mg/mL,respectively.At 1/2 MIC(non-inhibitory to bacterial growth),RGG significantly outperformed PGK and KGG in biofilm inhibition(P<0.05).Collectively,targeted peptide RGG competitively displaces AHL signal molecules from the LuxR protein of P.psychrophila,thereby attenuating biofilm formation.These findings provide a theoretical foundation for the rapid screening of peptide-based QS inhibitors against this psychrophilic spoilage bacterium.
张文熹;李鹏程;宋茹
浙江海洋大学食品与药学学院,浙江 舟山 316022浙江海洋大学食品与药学学院,浙江 舟山 316022浙江海洋大学食品与药学学院,浙江 舟山 316022
农业科技
冷藏鱿鱼嗜冷假单胞菌群体感应信号分子分子对接LuxR 蛋白靶向肽生物被膜
refrigerated squidPseudomonas psychrophilaquorum sensingsignal moleculesmolecular dockingLuxR pro-tein-targeted peptidesbiofilm
《水产学报》 2026 (9)
72-86,15
国家自然科学基金(32272374) National Natural Science Foundation of China(32272374)
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