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首页> 外文期刊>International Journal of Biochemistry Research & Review >Identification, Characterization and Purification of MSC_0265, a Potential Immunogenic Antigen Homologue of Mycoplasma mycoides subsp. mycoides in Mycoplasma capricolum subsp. capripneumoniae
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Identification, Characterization and Purification of MSC_0265, a Potential Immunogenic Antigen Homologue of Mycoplasma mycoides subsp. mycoides in Mycoplasma capricolum subsp. capripneumoniae

机译:MSC_0265的鉴定,表征和纯化,支原体支原体亚种的潜在免疫原性抗原同源物。支原体亚种中的杀菌剂肺炎克雷伯菌

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In silico identification and characterization of vaccine antigens has opened up new frontiers in the field of reverse vaccinology to mitigate the effects of livestock diseases by development of new subunit vaccines. This study aims to characterize, express and purify MSC_0265 for eventual use in immunoassays and inoculation in goats. Mycoplasma mycoides subs. mycoides ( Mmm ) and Mycoplasma capricolum capripneumoniae (Mccp) are similar pathogens on the genomic level and are the causative agents of Contagious Bovine Pleuropneumonia (CBPP) in cattle and Contagious Caprine Pleuropneumonia (CCPP) in goats respectively. In this study, BLAST was used to identify the homology of MSC_0265 in Mycoplasma capricolum capripneumoniae genome and the protein it is similar to. Characterization of MSC_0265 was also done using I-TASSER to predict secondary structure, solvent accessibility, normalised B-factor, 3D models and function. With cut off points of 0.0 for E-value, 100% for Query coverage and 90% for Identity, MSC_0265 a pyruvate dehydrogenase enzyme gave a high homology score on tBLASTn and BLASTp. It had earlier been cloned in pGS21a vector before proceeding with expression and purification of the His-tagged protein by Ni-NTA affinity chromatography. This study identified the homologue of MSC_0265 as protein WP_029333261.1 in the Mycoplasma capricolum capripneumoniae genome (Accession NZ_LN515398.1) using tBLASTn and BLASTp. Additionally, MSC_0265 was characterized and its optimal expression profile and estimated molecular weight verified.
机译:在计算机上对疫苗抗原的鉴定和表征在反向疫苗学领域开辟了新的领域,以通过开发新的亚单位疫苗来减轻家畜疾病的影响。这项研究旨在鉴定,表达和纯化MSC_0265,以最终用于山羊的免疫测定和接种。支原体支原体。在基因组水平上,杀真菌剂(Mmm)和猪肺炎支原体(Mccp)是相似的病原体,分别是牛的牛传染性胸膜肺炎(CBPP)和山羊的牛传染性胸膜肺炎(CCPP)的病原体。在这项研究中,BLAST被用于鉴定羊膜支原体肺炎支原体基因组中MSC_0265的同源性及其相似的蛋白质。还使用I-TASSER进行了MSC_0265的表征,以预测二级结构,溶剂可及性,标准化的B因子,3D模型和功能。 E值的截止点为0.0,查询覆盖率为100%,同一性为90%,丙酮酸脱氢酶MSC_0265在tBLASTn和BLASTp上具有很高的同源性评分。先前已将其克隆到pGS21a载体中,然后再通过Ni-NTA亲和色谱法表达和纯化His-tagged蛋白。这项研究使用tBLASTn和BLASTp将MSC_0265的同系物鉴定为衣原体支原体肺炎支原体基因组(登录号NZ_LN515398.1)中的WP_029333261.1蛋白。此外,表征了MSC_0265,并验证了其最佳表达谱和估计的分子量。

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