Self-assembled G-quadruplex nanostructures: AFM and voltammetric characterization

被引:46
作者
Chiorcea-Paquim, Ana-Maria [1 ]
Santos, Paulina Viegas [1 ]
Eritja, Ramon [2 ]
Oliveira-Brett, Ana Maria [1 ]
机构
[1] Univ Coimbra, Dept Quim, Fac Ciencias & Tecnol, Coimbra, Portugal
[2] CIBER BBN Networking Ctr Bioengn Biomat & Nanomed, IQAC CSIC, Inst Res Biomed, Barcelona, Spain
关键词
TETRAMOLECULAR G-QUADRUPLEXES; ATOMIC-FORCE MICROSCOPY; CRYSTAL-STRUCTURE; DNA-SEQUENCES; ADSORPTION;
D O I
10.1039/c3cp50866h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
G-rich oligodeoxynucleotides (ODNs) have great medical and nanotechnological potential, because they can self-assemble into G-quadruplexes and higher-order nanostructures. The folding properties of d(G)(10), d(TG(9)) and d(TG(8)T) ODNs were studied using atomic force microscopy (AFM) and voltammetry at carbon electrodes. Single-stranded ODNs, in Na+ containing solutions and for short incubation times, were detected using AFM as network films and polymeric structures and using voltammetry by the occurrence of only the guanine oxidation peak. G-quadruplexes, in Na+ containing solutions and long incubation times, or in K+ containing solutions, were detected using AFM as spherical aggregates and using voltammetry by the decrease of the guanine oxidation peak and the occurrence of the G-quartet oxidation peak. Concerning the self-assembling into higher-order nanostructures, d(G)(10) was the only sequence forming G-nanowires observed using AFM, d(TG(9)) formed short G-based super-structures that adsorbed as rod-like shape aggregates, and d(TG(8)T) formed no nanostructures, due to the presence of thymine residues at both 5' and 3' ends.
引用
收藏
页码:9117 / 9124
页数:8
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