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G-rich VEGF aptamer with locked and unlocked nucleic acid modifications exhibits a unique G-quadruplex fold

机译:具有锁定和未锁定核酸修饰的富含G的VEGF适体表现出独特的G-四链体折叠

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摘要

The formation of a single G-quadruplex structure adopted by a promising 25 nt G-rich vascular endothelial growth factor aptamer in a K+ rich environment was facilitated by locked nucleic acid modifications. An unprecedented all parallel-stranded monomeric G-quadruplex with three G-quartet planes exhibits several unique structural features. Five consecutive guanine residues are all involved in G-quartet formation and occupy positions in adjacent DNA strands, which are bridged with a no-residue propeller-type loop. A two-residue D-shaped loop facilitates inclusion of an isolated guanine residue into the vacant spot within the G-quartet. The remaining two G-rich tracts of three residues each adopt parallel orientation and are linked with edgewise and propeller loops. Both 5′ with 3 nt and 3′ with 4 nt overhangs display well-defined conformations, with latter adopting a basket handle topology. Locked residues contribute to thermal stabilization of the adopted structure and formation of structurally pre-organized intermediates that facilitate folding into a single G-quadruplex. Understanding the impact of chemical modifications on folding, thermal stability and structural polymorphism of G-quadruplexes provides means for the improvement of vascular endothelial growth factor aptamers and advances our insights into driving nucleic acid structure by locking or unlocking the conformation of sugar moieties of nucleotides in general.
机译:锁定的核酸修饰促进了有希望的25 nt富含G的血管内皮生长因子适体在富K + s的环境中采用的单个G-四链体结构的形成。前所未有的全平行单链单体G-四联体与三个G-四联体平面表现出几个独特的结构特征。五个连续的鸟嘌呤残基均参与G四联体的形成并占据相邻DNA链中的位置,这些DNA链与无残基的螺旋桨型环桥接。两个残基的D形环有助于将孤立的鸟嘌呤残基包含到G四重奏的空位中。其余的三个残基的两个富含G的区域均采用平行方向,并与边环和螺旋桨环相连。具有3 nt的5'和具有4 nt的3'突出端均显示良好定义的构型,后者采用篮状手柄拓扑。锁定的残基有助于所采用结构的热稳定和结构上预先组织好的中间体的形成,这些中间体有利于折叠成单个G-四链体。了解化学修饰对G-四链体的折叠,热稳定性和结构多态性的影响为改善血管内皮生长因子适体提供了手段,并通过锁定或解锁核苷酸中糖基部分的构象来推动我们对驱动核酸结构的见解。一般。

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