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兼职蛋白作为潜在抗原靶点的分子鉴定及生物信息学分析

Molecular Identification and Bioinformatics Analysis of Moonlighting Proteins as Possible Antigenic Targets.

作者信息

Quiroz-Castañeda Rosa Estela, Aguilar-Díaz Hugo, Coronado-Villanueva Eduardo, Catalán-Ochoa Diego Israel, Amaro-Estrada Itzel

机构信息

Centro Nacional de Investigación Disciplinaria en Salud Animal e Inocuidad, Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias (CENID-SAI, INIFAP), Jiutepec 62574, México.

出版信息

Pathogens. 2024 Sep 28;13(10):845. doi: 10.3390/pathogens13100845.

Abstract

BACKGROUND

Diseases of veterinary importance, such as bovine Anaplasmosis, cause significant economic losses. Due to this, the study of various proteins of the causal agent has focused on surface proteins. However, a vaccine for this disease is not yet available. To this end, in this work, moonlighting proteins (MLPs) are presented as an alternative approach for the design of immunogens against .

METHODS

The proteins of the strain MEX-15-099-01 were analyzed, and its MLPs were identified. Subsequently, four virulence-associated MLP genes were selected and identified using PCR. The proteins were analyzed using a structural homology approach and the collection of B-cell epitopes was predicted for each MLP. Finally, a pair of AmEno peptides were synthesized and the antigenic potential was tested using an iELISA.

RESULTS

Our bioinformatics analysis revealed the potential of AmEno, AmGroEl, AmEF-Tu, and AmDnaK proteins as promising candidates for designing immunogens. The PCR allowed the gene sequence identification in the genome of the strain MEX-15-099-01. Notably, AmEno-derived synthetic peptides showed antigenicity in an ELISA.

CONCLUSIONS

Our study has shed light on the potential use of MLPs for immunogen design, demonstrating the antigenic potential of AmEno.

摘要

背景

诸如牛无形体病等具有兽医重要性的疾病会造成重大经济损失。因此,对病原体各种蛋白质的研究主要集中在表面蛋白上。然而,目前尚无针对该疾病的疫苗。为此,在本研究中,兼职蛋白(MLP)被提出作为设计抗该疾病免疫原的一种替代方法。

方法

对菌株MEX - 15 - 099 - 01的蛋白质进行分析,并鉴定其兼职蛋白。随后,使用聚合酶链反应(PCR)选择并鉴定了四个与毒力相关的兼职蛋白基因。采用结构同源性方法对这些蛋白质进行分析,并预测每个兼职蛋白的B细胞表位。最后,合成了一对AmEno肽,并使用间接酶联免疫吸附测定(iELISA)检测其抗原潜力。

结果

我们的生物信息学分析表明,AmEno、AmGroEl、AmEF - Tu和AmDnaK蛋白有潜力成为设计免疫原的理想候选物。PCR技术实现了对菌株MEX - 15 - 099 - 01基因组中基因序列的鉴定。值得注意的是,源自AmEno的合成肽在酶联免疫吸附测定中显示出抗原性。

结论

我们的研究揭示了兼职蛋白在免疫原设计中的潜在用途,证明了AmEno的抗原潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bd2/11510912/cebb39198cc7/pathogens-13-00845-g001.jpg

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