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抗DNA抗体抗原选择的遗传和结构证据。

Genetic and structural evidence for antigen selection of anti-DNA antibodies.

作者信息

Radic M Z, Weigert M

机构信息

Department of Microbiology and Immunology, Medical College of Pennsylvania, Philadelphia 19129.

出版信息

Annu Rev Immunol. 1994;12:487-520. doi: 10.1146/annurev.iy.12.040194.002415.

Abstract

The primary structure of anti-DNA antibodies is highly diverse, a result of different germline variable (V) gene use, different combinations of immunoglobulin gene segments, peculiar heavy chain complementarity determining region 3 (H-CDR3) segments, and somatic mutations. Nevertheless, tertiary structure predictions reveal common features that yield information about likely contact sites in the anti-DNA combining site. That these contacts are involved with DNA binding is supported by recurrent features of a newly compiled set of homology groups of 13 variable regions of heavy chains (VH) and 11 variable regions of light chains (VL), characteristic pattern of somatic mutations, and the results of site-directed mutagenesis. The role of antigen in the etiology of the autoimmune response is viewed in light of recent data on overlaps between anti-DNA and anti-nucleic acid binding protein specificities.

摘要

抗DNA抗体的一级结构高度多样,这是不同种系可变(V)基因的使用、免疫球蛋白基因片段的不同组合、独特的重链互补决定区3(H-CDR3)片段以及体细胞突变的结果。然而,三级结构预测揭示了一些共同特征,这些特征提供了有关抗DNA结合位点中可能的接触位点的信息。一组新汇编的由13个重链可变区(VH)和11个轻链可变区(VL)组成的同源组的反复出现的特征、体细胞突变的特征模式以及定点诱变的结果支持了这些接触与DNA结合有关。根据抗DNA和抗核酸结合蛋白特异性之间重叠的最新数据,探讨了抗原在自身免疫反应病因中的作用。

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