Institute for Advanced Chemistry of Catalonia (IQAC), CSIC, Jordi Girona 18-26, 08034 Barcelona, Spain; Networking Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Jordi Girona 18-26, 08034 Barcelona, Spain.
Department of Food, Environmental and Nutritional Sciences (DEFENS), Section of Chemical and Biomolecular Sciences, University of Milan, Via Celoria 2, 20133 Milan, Italy.
Biochim Biophys Acta Gen Subj. 2017 May;1861(5 Pt B):1205-1212. doi: 10.1016/j.bbagen.2016.09.030. Epub 2016 Oct 2.
Guanine-rich oligonucleotides are capable of forming tetrahelical structures known as G-quadruplexes with interesting biological properties. We have investigated the effects of site-specific substitution in the loops and in the tetrads model G-quadruplexes using thymine glycol nucleic acid (GNA) units, l-thymidine and 8-Br-2'-deoxyguanosine.
Modified oligonucleotides were chemically synthesized and spectroscopic techniques were used to determine the relative stability of the modified G-quadruplex. The double 8-BrdG-modified quadruplexes were further characterized by Nuclear Magnetic Resonance. Binding to thrombin of selected quadruplex was analyzed by gel electrophoresis retention assay.
The most interesting results were found with a 8-bromoG substitution that had the larger stabilization of the quadruplex. NMR studies indicate a tight relationship between the loops and the tetrads to accommodate 8-bromoG modifications within the TBA.
The substitutions of loop positions with GNA T affect the TBA stability except for single modification in T7 position. Single l-thymidine substitutions produced destabilization of TBA. Larger changes on quadruplex stability are observed with the use of 8-bromoG finding a single substitution with the highest thermal stabilization found in thrombin binding aptamers modified at the guanine residues and having good affinity for thrombin. Double 8-BrdG modification in anti positions of different tetrads produce a conformational flip from syn to anti conformation of 8-Br-dG to favor loop-tetrad interaction and preserve the overall TBA stability.
Modified guanine-rich oligonucleotides are valuable tools for the search for G-quadruplex structures with higher thermal stability and may provide compounds with interesting protein-nucleic acid binding properties. This article is part of a Special Issue entitled "G-quadruplex" Guest Editor: Dr. Concetta Giancola and Dr. Daniela Montesarchio.
富含鸟嘌呤的寡核苷酸能够形成具有有趣生物学特性的四链体结构,称为 G-四链体。我们已经研究了胸腺嘧啶二醇核酸 (GNA) 单元、L-胸苷和 8-Br-2'-脱氧鸟苷在环和四联体模型 G-四链体中的定点取代对 G-四链体的影响。
化学合成修饰的寡核苷酸,并使用光谱技术确定修饰的 G-四链体的相对稳定性。进一步通过核磁共振对双 8-BrdG 修饰的四联体进行了表征。通过凝胶电泳保留试验分析了选定四联体与凝血酶的结合。
最有趣的结果是在 8-溴 G 取代时发现,四联体的稳定性有较大提高。NMR 研究表明,环与四联体之间存在紧密关系,以适应 TBA 内的 8-溴 G 修饰。
用 GNA T 取代环位置会影响 TBA 的稳定性,除了 T7 位置的单个修饰外。单个 L-胸苷取代会导致 TBA 失稳。使用 8-溴 G 会观察到四联体稳定性的更大变化,在修饰鸟嘌呤残基的凝血酶结合适体中发现单个取代具有最高的热稳定性,并与凝血酶具有良好的亲和力。不同四联体反位的双 8-BrdG 修饰会导致 8-Br-dG 从顺式到反式构象的构象翻转,有利于环-四联体相互作用并保持整体 TBA 稳定性。
修饰的富含鸟嘌呤的寡核苷酸是寻找具有更高热稳定性的 G-四链体结构的有价值工具,可能提供具有有趣的蛋白质-核酸结合特性的化合物。本文是题为“G-四链体”的特刊的一部分,客座编辑:Concetta Giancola 博士和 Daniela Montesarchio 博士。