Foster M H, Kieber-Emmons T, Ohliger M, Madaio M P
Penn Center for Molecular Studies of Kidney Diseases, University of Pennsylvania, Philadelphia 19104-6144, USA.
Immunol Res. 1994;13(2-3):186-206. doi: 10.1007/BF02918279.
To determine the structure of three nuclear localizing lupus anti-DNA immunoglobulins (Igs) and to search for clues to mechanisms of cellular and/or nuclear access, their H- and L-chain variable region sequences were determined and subjected to three-dimensional modeling. Although the results indicate heterogeneity in their primary structures, the H chains are encoded by 3 members of the J558 VH gene family with a common tertiary conformation that is not shared by a J558-encoded nonnuclear localizing anti-DNA control Ig. Furthermore, at least two of the Igs share a conformational motif in the H-chain CDR3, and all three Igs contain multiple positively charged amino acids in their CDRs, resembling nuclear localization signals that direct protein nuclear import. Notably, each VH and VK gene is also found recurrently among previously described autoantibodies. Molecular analysis further indicates that both germline-encoded and significantly mutated V genes can generate nuclear localizing anti-DNA Ig.
为了确定三种核定位狼疮抗DNA免疫球蛋白(Igs)的结构,并寻找细胞和/或核进入机制的线索,我们测定了它们的重链和轻链可变区序列,并进行了三维建模。尽管结果表明它们的一级结构存在异质性,但重链由J558 VH基因家族的3个成员编码,具有共同的三级构象,而J558编码的非核定位抗DNA对照Ig不具有这种构象。此外,至少有两种Ig在重链互补决定区3(CDR3)中共享一个构象基序,并且所有三种Ig在其CDR中都含有多个带正电荷的氨基酸,类似于指导蛋白质核输入的核定位信号。值得注意的是,每个VH和VK基因在先前描述的自身抗体中也反复出现。分子分析进一步表明,种系编码和显著突变的V基因都可以产生核定位抗DNA Ig。