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针对硫代磷酸酯和核糖修饰DNA产生的单克隆抗体的特异性。

Specificity of monoclonal antibodies produced against phosphorothioate and ribo modified DNAs.

作者信息

Latimer L J, Agazie Y M, Braun R P, Hampel K J, Lee J S

机构信息

Department of Biochemistry, University of Saskatchewan, Saskatoon, Canada.

出版信息

Mol Immunol. 1995 Oct;32(14-15):1057-64. doi: 10.1016/0161-5890(95)00086-0.

Abstract

A large number of phosphorothioate DNAs and mixed ribo/deoxyribo duplexes were prepared and their immunogenicity was studied in mice. Only those polymers which were nuclease-resistant were immunogenic and in these cases monoclonal antibodies were prepared. The specificity of the antibodies was measured by direct and competitive Solid Phase Radioimmune Assay (SPRIA) and on this basis four types of antibody could be identified. Type I antibodies are specific for the immunizing polymer and show very limited crossreactivity. For example, Jel 384 binds only to poly(dsA).poly(dT); Jel 453 and 462 bind only to poly(dsG).poly(dC) and poly(dsG).poly(dm5C). Type II antibodies bind to most polymers containing the appropriate modification but will not bind to unmodified DNAs. For example, Jel 343 binds to most thio DNAs regardless of sequence; Jel 346 binds well to most ribose-containing polymers and may be a useful reagent for the detection of the 'A' family of conformations. Type III antibodies bind to most nucleic acids whether modified or not. Their specificities are similar to autoimmune antibodies. Type IV antibodies are single strand-specific such as Jel 383 which binds to poly(dT). There were no examples of antibodies which bound specifically to the immunizing DNA and the unmodified polymer. Thus, modified DNAs cannot be used to prepare sequence-specific reagents. Also, the immunogenicity of modified nucleic acids may limit their usefulness in antisense technologies.

摘要

制备了大量硫代磷酸酯DNA和核糖/脱氧核糖混合双链体,并在小鼠中研究了它们的免疫原性。只有那些抗核酸酶的聚合物具有免疫原性,在这些情况下制备了单克隆抗体。通过直接和竞争性固相放射免疫测定法(SPRIA)测定抗体的特异性,在此基础上可鉴定出四种类型的抗体。I型抗体对免疫聚合物具有特异性,交叉反应性非常有限。例如,Jel 384仅与聚(dsA)·聚(dT)结合;Jel 453和462仅与聚(dsG)·聚(dC)和聚(dsG)·聚(dm5C)结合。II型抗体与大多数含有适当修饰的聚合物结合,但不与未修饰的DNA结合。例如,Jel 343与大多数硫代DNA结合,与序列无关;Jel 346与大多数含核糖的聚合物结合良好,可能是检测“A”型构象的有用试剂。III型抗体与大多数核酸结合,无论其是否修饰。它们的特异性类似于自身免疫抗体。IV型抗体是单链特异性的,如与聚(dT)结合的Jel 383。没有抗体特异性结合免疫DNA和未修饰聚合物的例子。因此,修饰的DNA不能用于制备序列特异性试剂。此外,修饰核酸的免疫原性可能会限制它们在反义技术中的应用。

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