Störl H J, Simon H, Barthelmes H
Acta Biol Med Ger. 1979;38(7):1055-61.
Oligodeoxyribonucleotides act as inhibitors of the complement fixation caused by complexes between antibodies to defined oligodeoxyribonucleotides and denatured DNA. At concentrations higher than 50 micrograms oligodeoxyribonucleotide/ml complement fixation occurred in the absence of antigen. The extent of complement binding depends on the specificity of the antibodies as well as on the composition of the oligodeoxyribonucleotides. Complement fixation is observed most strongly with antisera to oligodeoxyribonucleotides and to denatured DNA, which belong predominantly to the IgM class. With two LE-sera, containing antibodies to denatured and to native DNA, no complement fixation was found. It is supposed that specific interactions of the oligodeoxyribonucleotides with amino acid residues closely neighbored to the antibody combining site lead to conformational changes in the antibody molecules and to an activation of the complement binding site.
寡脱氧核糖核苷酸可作为补体固定的抑制剂,该补体固定由针对特定寡脱氧核糖核苷酸的抗体与变性DNA之间的复合物所引起。当浓度高于50微克寡脱氧核糖核苷酸/毫升时,在无抗原的情况下也会发生补体固定。补体结合的程度取决于抗体的特异性以及寡脱氧核糖核苷酸的组成。用主要属于IgM类的针对寡脱氧核糖核苷酸和变性DNA的抗血清观察到最强的补体固定。对于两种含有针对变性DNA和天然DNA抗体的狼疮血清,未发现补体固定。据推测,寡脱氧核糖核苷酸与紧邻抗体结合位点的氨基酸残基的特异性相互作用会导致抗体分子的构象变化以及补体结合位点的激活。