与因子 B 结合的 DNA Aptamer 家族的抑制作用超越了与非典型溶血性尿毒症相关的因子 B 变异的功能增益。

IF 3.6 3区 医学 Q2 IMMUNOLOGY
Huiquan Duan, Ying Zhang, Matthew R Otis, Daniel W Drolet, Brian V Geisbrecht
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引用次数: 0

摘要

多聚物是短的单链寡核苷酸,可选择性地与目标生物分子结合。虽然它们通常表现出良好的结合特异性,但由于核酸中相对缺乏疏水基团,它们的亲和力往往受到限制。为了克服这一障碍,人们合成了在尿嘧啶中加入疏水结构的化学修饰核苷酸。目前已针对 20 多种不同的补体蛋白开发出含有此类非标准核苷酸的修饰 DNA 合体。这些修饰的适配体显示出更强的亲和力和血清稳定性,具有潜在的治疗价值。最近,我们对能与补体因子 B(FB)特异性结合的修饰 DNA 合体家族进行了结构/功能研究。这项研究发现,这些适配体通过阻止补体成分 C3(C3)原转化酶复合物 C3bB 的形成,选择性地抑制了补体替代途径(AP)。某些非典型溶血性尿毒症患者表达的 FB 功能增益变体会增强原转化酶复合物的形成和/或降低内源性调节剂对其形成的 C3 转化酶的作用。为了研究这些与 FB 结合的适配体是否能超越 FB 致病突变的影响,我们在各种补体功能测试中研究了它们与几种 FB 变体(包括 D279G、F286L、K323E 和 K350N)的相互作用。我们发现,FB 结合型适配体的抑制作用超过了 FB 的功能增益突变,尽管适配体不能分解预形成的 C3 转化酶。这些研究结果表明,FB结合适配体可进一步开发为治疗某些非典型溶血性尿毒症患者或其他补体活性过高疾病的潜在疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Inhibitory Effects of a Factor B-Binding DNA Aptamer Family Supersede the Gain of Function of Factor B Variants Associated with Atypical Hemolytic Uremic Syndrome.

Aptamers are short, single-stranded oligonucleotides that selectively bind to target biomolecules. Although they generally exhibit good binding specificity, their affinities are often limited because of the relative lack of hydrophobic groups in nucleic acids. Chemically modified nucleotides incorporating hydrophobic structures into uracil have been synthesized to address this obstacle. Modified DNA aptamers containing such nonstandard nucleotides have been developed for >20 different complement proteins. These modified aptamers show increased affinity and enhanced serum stability and have potential value as therapeutic agents. We recently conducted a structure/function study on a family of modified DNA aptamers that bind specifically to complement Factor B (FB). This work revealed that these aptamers selectively inhibit the complement alternative pathway (AP) by preventing the formation of the AP complement component C3 (C3) proconvertase complex, C3bB. Certain patients with atypical hemolytic uremic syndrome express gain-of-function variants of FB that enhance the formation of the proconvertase complex and/or decrease the efficacy of endogenous regulators against the C3 convertases they form. To investigate whether these FB-binding aptamers could override the effects of disease-causing mutations in FB, we examined how they interacted with several FB variants, including D279G, F286L, K323E, and K350N, in various assays of complement function. We found that the inhibitory effect of the FB-binding aptamers superseded the gain-of-function mutations in FB, although the aptamers could not dissociate preformed C3 convertases. These findings suggest that FB-binding aptamers could be further developed as a potential treatment for certain atypical hemolytic uremic syndrome patients or those with other diseases characterized by excessive complement activity.

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来源期刊
Journal of immunology
Journal of immunology 医学-免疫学
CiteScore
8.20
自引率
2.30%
发文量
495
审稿时长
1 months
期刊介绍: The JI publishes novel, peer-reviewed findings in all areas of experimental immunology, including innate and adaptive immunity, inflammation, host defense, clinical immunology, autoimmunity and more. Special sections include Cutting Edge articles, Brief Reviews and Pillars of Immunology. The JI is published by The American Association of Immunologists (AAI)
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