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通过单克隆抗体和多克隆抗体鉴定MAGE-1基因产物。

Identification of the MAGE-1 gene product by monoclonal and polyclonal antibodies.

作者信息

Chen Y T, Stockert E, Chen Y, Garin-Chesa P, Rettig W J, van der Bruggen P, Boon T, Old L J

机构信息

Ludwig Institute for Cancer Research, New York Unit, NY.

出版信息

Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):1004-8. doi: 10.1073/pnas.91.3.1004.

Abstract

The human MAGE-1 gene encodes a melanoma peptide antigen recognized by autologous cytotoxic T lymphocytes. To produce antibodies against the MAGE-1 gene product, several approaches were taken. Three oligopeptides were synthesized based on predicted MAGE-1 amino acid sequences and were used to generate rabbit anti-peptide anti-sera. In addition, a truncated MAGE-1 cDNA was cloned into an Escherichia coli expression vector, and recombinant protein was produced and purified. All three rabbit anti-peptide antisera showed reactivity against the immunizing peptide, and one reacted with the recombinant MAGE-1 protein by immunoblotting, but none reacted with cell lysates from MAGE-1 mRNA-positive cells. The recombinant MAGE-1 protein was then used for the generation of mouse monoclonal and rabbit polyclonal antibodies. One IgG1 monoclonal antibody, MA454, as well as rabbit polyclonal antisera recognized a 46-kDa protein in extracts of MAGE-1 mRNA-positive melanoma cell lines. The antibodies showed no apparent cross-reactivity with products of the closely related MAGE-2 and MAGE-3 genes. Serological typing of normal and tumor cell lysates was in full agreement with mRNA analysis, showing expression of MAGE-1 protein in MAGE-1 mRNA-positive testis and a subset of melanomas but not in MAGE-1 mRNA-negative normal or tumor tissues. Transfection of the MAGE-1 gene into a MAGE-1 mRNA-negative melanoma cell line resulted in the expression of the 46-kDa protein, confirming the identity of this protein as the MAGE-1 gene product.

摘要

人类MAGE-1基因编码一种可被自体细胞毒性T淋巴细胞识别的黑色素瘤肽抗原。为了制备针对MAGE-1基因产物的抗体,研究人员采取了多种方法。基于预测的MAGE-1氨基酸序列合成了三种寡肽,并用于制备兔抗肽抗血清。此外,将截短的MAGE-1 cDNA克隆到大肠杆菌表达载体中,生产并纯化了重组蛋白。所有三种兔抗肽抗血清均显示出对免疫肽的反应性,其中一种通过免疫印迹与重组MAGE-1蛋白发生反应,但均未与MAGE-1 mRNA阳性细胞的细胞裂解物发生反应。然后,将重组MAGE-1蛋白用于制备小鼠单克隆抗体和兔多克隆抗体。一种IgG1单克隆抗体MA454以及兔多克隆抗血清识别出MAGE-1 mRNA阳性黑色素瘤细胞系提取物中的一种46 kDa蛋白。这些抗体与密切相关的MAGE-2和MAGE-3基因的产物没有明显的交叉反应。正常细胞和肿瘤细胞裂解物的血清学分型与mRNA分析完全一致,表明MAGE-1蛋白在MAGE-1 mRNA阳性的睾丸和一部分黑色素瘤中表达,但在MAGE-1 mRNA阴性的正常或肿瘤组织中不表达。将MAGE-1基因转染到MAGE-1 mRNA阴性的黑色素瘤细胞系中导致46 kDa蛋白的表达,证实了该蛋白为MAGE-1基因产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c4/521442/cd864ebf270f/pnas01125-0181-a.jpg

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