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结核分枝杆菌多种抗原融合蛋白用于活动性结核病的血清学诊断评估。

Serodiagnostic evaluation of fusion proteins from multiple antigens of Mycobacterium tuberculosis for active TB.

机构信息

School of Biological Sciences, University of the Punjab, Lahore, Pakistan.

Armed Forces Institute of Pathology, Rawalpindi, Pakistan.

出版信息

Tuberculosis (Edinb). 2021 Mar;127:102053. doi: 10.1016/j.tube.2021.102053. Epub 2021 Feb 2.

Abstract

Tuberculosis (TB) is a global health problem, being prevalent in the developing countries. A rapid, reliable and cost effective diagnostic method would help in controlling TB in the endemic populations. Development of suitable fusion molecules detecting multiple antibodies produced against Mycobacterium tuberculosis antigens would enhance sensitivity of serodiagnostic assays. In this study, EspC, CFP7 and PPE57 antigens of M. tuberculosis were selected for constructing fusion molecules after prediction of B-cell epitopes using in silico tools. Fusion proteins EspC-CFP7, HspX-EspC-CFP7 and HspX-EspC-CFP7-PPE57 were expressed in E.coli (BL21). The serodiagnostic potential of the individual antigens and their fusions was analyzed by screening 230 plasma samples of pulmonary TB patients. The single antigens HspX, EspC, CFP7, PPE57 showed sensitivities of 30%, 31%, 22% and 35%, respectively. The fusion protein EspC-CFP7 showed sensitivity of 43%. Linking of HspX antigen to the N-terminus of EspC-CFP7 fusion molecule increased sensitivity to 58%, while joining PPE57 antigen to the C-terminus of HspX-EspC-CFP7 increased sensitivity to 69%. The fusion protein HspX-EspC-CFP7-PPE57 seems to be a promising molecule for use in the development of fusions with higher sensitivity.

摘要

结核病(TB)是一个全球性的健康问题,在发展中国家更为普遍。一种快速、可靠且具有成本效益的诊断方法将有助于控制流行地区的结核病。开发能够检测针对结核分枝杆菌抗原的多种抗体的合适融合分子将提高血清学诊断检测的敏感性。在这项研究中,使用计算机工具预测了 B 细胞表位后,选择了结核分枝杆菌的 EspC、CFP7 和 PPE57 抗原用于构建融合分子。融合蛋白 EspC-CFP7、HspX-EspC-CFP7 和 HspX-EspC-CFP7-PPE57 在大肠杆菌(BL21)中表达。通过筛选 230 份肺结核患者的血浆样本,分析了单个抗原及其融合体的血清学诊断潜力。单个抗原 HspX、EspC、CFP7 和 PPE57 的敏感性分别为 30%、31%、22%和 35%。融合蛋白 EspC-CFP7 的敏感性为 43%。将 HspX 抗原连接到 EspC-CFP7 融合分子的 N 端可将敏感性提高到 58%,而将 PPE57 抗原连接到 HspX-EspC-CFP7 的 C 端可将敏感性提高到 69%。融合蛋白 HspX-EspC-CFP7-PPE57 似乎是一种很有前途的分子,可用于开发具有更高敏感性的融合蛋白。

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