Stabilization and Induction of Oligonucleotide i-Motif Structure via Graphene Quantum Dots

被引:50
作者
Chen, Xin [1 ]
Zhou, Xuejiao [2 ]
Han, Ting [2 ]
Wu, Jiaying [1 ]
Zhang, Jingyan [1 ]
Guo, Shouwu [2 ]
机构
[1] E China Univ Sci & Technol, Shanghai Key Lab New Drug Design, State Key Lab Bioreactor Engn, Sch Pharm, Shanghai 200237, Peoples R China
[2] Shanghai Jiao Tong Univ, Key Lab Thin Film & Microfabricat, Minist Educ, Res Inst Micro Nano Sci & Technol, Shanghai 200240, Peoples R China
基金
美国国家科学基金会;
关键词
graphene quantum dots; i-motif; stabilization; induction; end-stacking; G-QUADRUPLEX; TELOMERIC DNA; FLUORESCENCE; 2-AMINOPURINE; TELOMESTATIN;
D O I
10.1021/nn304673a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
DNA i-motif structures have been found in telomeric, centromeric DNA and many in the promoter region of oncogenes; thus they might be attractive targets for gene-regulation processes and anticancer therapeutics. We demonstrate in this work that i-motif structures can be stabilized by graphene quantum dots (GQDs) under acidic conditions, and more importantly GODs can promote the formation of the i-motif structure under alkaline or physiological conditions. We Illustrate that the GQDs stabilize the i-motif structure through end-stacking of the bases at its loop regions, thus reducing its solvent-accessible area. Under physiological or alkaline conditions, the end-stacking of GQDs on the unfolded structure shifts the equilibrium between the I-motif and unfolded structure toward the i-motif structure, thus promoting its formation. The possibility of fine-tuning the stability of the I-motif and Inducing its formation would make GQDs useful in gene regulation and oligonucleotide-based therapeutics.
引用
收藏
页码:531 / 537
页数:7
相关论文
共 36 条
[1]   Interaction of an acridine dimer with DNA quadruplex structures [J].
Alberti, P ;
Ren, JS ;
Teulade-Fichou, MP ;
Guittat, L ;
Riou, JF ;
Chaires, JB ;
Hélène, C ;
Vigneron, JP ;
Lehn, JM ;
Mergny, JL .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2001, 19 (03) :505-513
[2]  
[Anonymous], 2002, JPEG2000 SIGNAL PROC
[3]   G-quadruplex nucleic acids as therapeutic targets [J].
Balasubramanian, Shankar ;
Neidle, Stephen .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2009, 13 (03) :345-353
[4]   Stabilization of the DNA I-motif structure by incorporation of 3′-S-phosphorothiolate linkages [J].
Brazier, JA ;
Fisher, J ;
Cosstick, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (01) :114-117
[5]   Making sense of G-quadruplex and i-motif functions in oncogene promoters [J].
Brooks, Tracy A. ;
Kendrick, Samantha ;
Hurley, Laurence .
FEBS JOURNAL, 2010, 277 (17) :3459-3469
[6]   Chemical nucleases [J].
Cowan, JA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2001, 5 (06) :634-642
[7]   A Direct and Nondestructive Approach To Determine the Folding Structure of the I-Motif DNA Secondary Structure by NMR [J].
Dai, Jixun ;
Ambrus, Attila ;
Hurley, Laurence H. ;
Yang, Danzhou .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (17) :6102-+
[8]   Cationic porphyrins promote the formation of i-motif DNA and bind peripherally by a nonintercalative mechanism [J].
Fedoroff, OY ;
Rangan, A ;
Chemeris, VV ;
Hurley, LH .
BIOCHEMISTRY, 2000, 39 (49) :15083-15090
[9]   A TETRAMERIC DNA-STRUCTURE WITH PROTONATED CYTOSINE.CYTOSINE BASE-PAIRS [J].
GEHRING, K ;
LEROY, JL ;
GUERON, M .
NATURE, 1993, 363 (6429) :561-565
[10]   The i-motif in nucleic acids [J].
Guéron, M ;
Leroy, JL .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (03) :326-331