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结直肠癌患者()和健康个体()肠道相关细菌中粘附毒力蛋白FadA的比较分析。

Comparative analysis of adhesion virulence protein FadA from gut-associated bacteria of colorectal cancer patients () and healthy individuals ().

作者信息

Hussain Nadia, Muccee Fatima, Ashraf Naeem Mahmood, Afsar Tayyaba, Husain Fohad Mabood, Hamid Arslan, Razak Suhail

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, Al Ain University, Al Ain Campus, Al Ain 64141, Abu Dhabi, United Arab Emirates.

AAU Health and Biomedical Research Center, Al Ain University, Abu Dhabi Campus, Abu Dhabi P. O. Box 112612, Abu Dhabi, United Arab Emirates.

出版信息

J Cancer. 2024 Aug 19;15(17):5492-5505. doi: 10.7150/jca.98951. eCollection 2024.

Abstract

Colorectal cancer (CRC) is a gastrointestinal disease linked with GIT microbial dysbiosis. The present study has targeted the comparative analysis of virulent factor FadA from gut-associated bacteria of CRC patients () and healthy individuals (). For this purpose, FadA protein sequences of fifteen strains of and four strains of , were retrieved from the UniProt database. These sequences were analysed through VirulentPred, PSLpred, ProtParam, PFP-FunDSeqE, PROTEUS Structure Prediction Server, SWISS-MODEL, SAVES validation server, MEME suite 5.5.0, CAVER Web tool, Webserver VaxinPAD, HPEPDOCK and HDOCK servers. FadA protein from was found to exhibit significant differences as compared to i.e. it exhibited helical configuration, cytoplasmic, periplasmic, outer-membrane and extracellular localisation, 2D structure comprising of 70-96% helix, 0% beta-sheet, 4-30% coils and 17-20 signal peptide residues, hydrophilicity, strongly acidic character and smaller number of antigenic epitopes. In contrast, FadA protein from was found to have globular 3D configuration, cytoplasmic localisation, 2D structure (30-56% helix, 12-21% beta-sheet, 33-50% coils and 43 signal peptide residues), highly hydrophobic, slightly acidic and more number of antigenic epitopes. Docking analyses of virulent factors revealed their high binding affinities with previously reported inhibitory peptide and FAD-approved drug COX2. The wide range of differences not only provided us the reason for the role of FadA protein as a virulent factor in but also might help us in designing virulent FadA protein inhibiting strategies including peptide-based vaccine adjuvants and drugs designing, modification of tunnels and catalytic pockets to reduce substrate binding and FAD approved drugs selection. Inhibition of this virulent factor in CRC patients' gut bacteria might result in oncogenesis regression and reduced death rate.

摘要

结直肠癌(CRC)是一种与胃肠道微生物群落失调相关的胃肠道疾病。本研究旨在对CRC患者()和健康个体()肠道相关细菌中的毒力因子FadA进行比较分析。为此,从UniProt数据库中检索了15株和4株的FadA蛋白序列。这些序列通过VirulentPred、PSLpred、ProtParam、PFP-FunDSeqE、PROTEUS结构预测服务器、SWISS-MODEL、SAVES验证服务器、MEME套件5.5.0、CAVER网络工具、Webserver VaxinPAD、HPEPDOCK和HDOCK服务器进行分析。结果发现,与相比,来自的FadA蛋白表现出显著差异,即它呈现螺旋结构、定位于细胞质、周质、外膜和细胞外,二维结构由70 - 96%的螺旋、0%的β-折叠、4 - 30%的卷曲和17 - 20个信号肽残基组成,具有亲水性、强酸性特征且抗原表位数量较少。相比之下,来自的FadA蛋白具有球状三维结构、定位于细胞质,二维结构(30 - 56%螺旋、12 - 21%β-折叠、33 - 50%卷曲和43个信号肽残基),高度疏水、微酸性且抗原表位数量较多。毒力因子的对接分析显示它们与先前报道的抑制肽和FAD批准的药物COX2具有高结合亲和力。这些广泛的差异不仅为我们提供了FadA蛋白作为毒力因子在中发挥作用的原因,还可能有助于我们设计抑制毒力FadA蛋白的策略,包括基于肽的疫苗佐剂和药物设计、修饰通道和催化口袋以减少底物结合以及选择FAD批准的药物。抑制CRC患者肠道细菌中的这种毒力因子可能会导致肿瘤发生消退并降低死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c2/11414602/83b8c28497ac/jcav15p5492g001.jpg

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