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针对烟曲霉58千道尔顿抗原的单克隆抗体的制备与特性分析

Production and characterization of monoclonal antibodies to a 58-kilodalton antigen of Aspergillus fumigatus.

作者信息

Fratamico P M, Long W K, Buckley H R

机构信息

Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.

出版信息

Infect Immun. 1991 Jan;59(1):316-22. doi: 10.1128/iai.59.1.316-322.1991.

Abstract

Eight monoclonal antibodies that recognize a serodiagnostically important 58-kDa antigen of Aspergillus fumigatus were produced and partially characterized. 2-7, 2-12, and 2-14 are of the immunoglobulin M class, and 2-2-1, 2-2-4, 2-2-6, 2-2-9, and 2-2-13 are all immunoglobulin G1(kappa) antibodies. Immunoblot analysis with A. fumigatus mycelial extract demonstrated that all of the monoclonal antibodies recognize a major 58-kDa antigen. The antigen was also detected by immunoblot analysis of 4- and 7-day culture filtrate preparations. 2-2-1, 2-2-4, and 2-2-6 cross-reacted with an antigen of approximately 55 kDa from an extract of Candida albicans. 2-7, 2-12, 2-14, and 2-2-4 formed a precipitin band with immunoaffinity-purified 58-kDa antigen by immunodiffusion. Results from indirect immunofluorescence assays with 2-7 and 2-2-9 showed fluorescent staining mainly on the surfaces of conidia and hyphae, indicating that the 58-kDa antigen may be cell wall associated. 2-2-9 and 2-2-13 and antibodies in patient and immune rabbit sera precipitated the [35S]methionine-labeled 58-kDa antigen. The 58-kDa antigen immunoprecipitated by each of the antibodies was enzymatically cleaved by Staphylococcus aureus V8 protease; one cleavage product, a 35-kDa fragment, was generated, indicating that the precipitated antigens share primary structure. Immunoblot analysis with an immunoaffinity-purified 58-kDa antigen showed that sera from patients with invasive aspergillosis reacted with the same antigen as that recognized by the monoclonal antibodies.

摘要

制备了8种识别烟曲霉血清学诊断重要的58 kDa抗原的单克隆抗体,并对其进行了部分特性鉴定。2-7、2-12和2-14属于免疫球蛋白M类,而2-2-1、2-2-4、2-2-6、2-2-9和2-2-13均为免疫球蛋白G1(κ)抗体。用烟曲霉菌丝体提取物进行免疫印迹分析表明,所有单克隆抗体均识别一种主要的58 kDa抗原。通过对4天和7天培养滤液制剂的免疫印迹分析也检测到了该抗原。2-2-1、2-2-4和2-2-6与白色念珠菌提取物中约55 kDa的抗原发生交叉反应。2-7、2-12、2-14和2-2-4通过免疫扩散与免疫亲和纯化的58 kDa抗原形成沉淀带。用2-7和2-2-9进行间接免疫荧光试验的结果显示,荧光染色主要出现在分生孢子和菌丝表面,表明58 kDa抗原可能与细胞壁相关。2-2-9和2-2-13以及患者和免疫兔血清中的抗体沉淀了[35S]甲硫氨酸标记的58 kDa抗原。每种抗体免疫沉淀的58 kDa抗原均被金黄色葡萄球菌V8蛋白酶酶切;产生了一种35 kDa的裂解产物,表明沉淀的抗原具有相同的一级结构。用免疫亲和纯化的58 kDa抗原进行免疫印迹分析表明,侵袭性曲霉病患者的血清与单克隆抗体识别的相同抗原发生反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ba9/257743/72277f56c089/iai00037-0338-a.jpg

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