journal article·2013-01-22

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

Xin Chen, Xuejiao Zhou, Ting Han, Jiaying Wu, Jingyan Zhang, Shouwu Guo

ACS Nano· Volume 7· Issue 1
Publisher page

Abstract

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 GQDs 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.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Graphene and Nanomaterials Applications · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Shanghai Key Laboratory of New Drug Design, State Key Laboratory of Bioreactor Engineering, School of Pharmacy, East China University of Science and Technology, Shanghai, 200237, People's Republic of China

Key Laboratory of Thin Film and Microfabrication of the Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai Jiao Tong University, Shanghai, 200240, People's Republic of China

References (36)

Show source-provided references
1. Phan A. T. · Nucleic Acids Res. · 2002 · 30 · 461810.1093/nar/gkf597 ↗
2. Gehring K. · Nature · 1993 · 363 · 56110.1038/363561a0 ↗
3. Kim M. Y. · J. Am. Chem. Soc. · 2002 · 124 · 209810.1021/ja017308q ↗
4. Rosu F. · Chem. Commun. · 2003 · 270210.1039/b309394h ↗
5. Balasubramanian S. · Curr. Opin. Chem. Biol. · 2009 · 13 · 34510.1016/j.cbpa.2009.04.637 ↗
6. Gueron M. · Curr. Opin. Struct. Biol. · 2000 · 10 · 32610.1016/S0959-440X(00)00091-9 ↗
7. Guo K. · J. Am. Chem. Soc. · 2007 · 129 · 1022010.1021/ja072185g ↗
8. Brooks T. A. · FEBS J. · 2010 · 277 · 345910.1111/j.1742-4658.2010.07759.x ↗
9. Han H. Y. · Trends Pharmacol. Sci. · 2000 · 21 · 13610.1016/S0165-6147(00)01457-7 ↗
10. Fedoroff O. Y. · Biochemistry · 2000 · 39 · 1508310.1021/bi001528j ↗
11. Alberti P. · J. Biomol. Struct. Dyn. · 2001 · 19 · 50510.1080/07391102.2001.10506758 ↗
12. Teulade-Fichou M. P. · J. Am. Chem. Soc. · 2003 · 125 · 473210.1021/ja021299j ↗
13. Li X. · Proc. Natl. Acad. Sci. U. S. A. · 2006 · 103 · 1965810.1073/pnas.0607245103 ↗
14. Cowan J. A. · Cur. Opin. Chem. Biol. · 2001 · 5 · 63410.1016/S1367-5931(01)00259-9 ↗
15. Zhang J. · Chem. Commun. · 2010 · 46 · 111210.1039/B917705A ↗
16. Ren H. · ACS Nano · 2010 · 4 · 716910.1021/nn101696r ↗
17. Zheng B. · J. Phys. Chem. C · 2012 · 116 · 1583910.1021/jp3050324 ↗
18. Zhou X. · ACS Nano · 2012 · 8 · 659210.1021/nn301629v ↗
19. Wu J. · Chem. Rev. · 2007 · 107 · 71810.1021/cr068010r ↗
20. Zhu S. · Chem. Commun. · 2011 · 47 · 685810.1039/c1cc11122a ↗
21. Robinson J. T. · J. Am. Chem. Soc. · 2011 · 133 · 682510.1021/ja2010175 ↗
22. Phan A. T. · J. Mol. Biol. · 2000 · 299 · 12310.1006/jmbi.2000.3613 ↗
23. Sun D. · J. Med. Chem. · 2009 · 52 · 286310.1021/jm900055s ↗
24. Li W. · FEBS Lett. · 2002 · 526 · 7710.1016/S0014-5793(02)03118-6 ↗
25. Jin K. S. · J. Phys. Chem. B · 2009 · 113 · 185210.1021/jp808186z ↗
26. Mergny J.-L. · J. Am. Chem. Soc. · 1995 · 117 · 888710.1021/ja00140a001 ↗
27. Jin K. S. · J. Phys. Chem. B · 2010 · 114 · 478310.1021/jp9122453 ↗
28. Ward D. C. · J. Biol. Chem. · 1969 · 244 · 122810.1016/S0021-9258(18)91833-8 ↗
29. Kimura T. · Chem. Commun. · 2004 · 143810.1039/b403913k ↗
30. Rosu F. · Biochemistry · 2003 · 42 · 1036110.1021/bi034531m ↗
31. Monchaud D. · Nucleosides, Nucleotides Nucleic Acids · 2007 · 26 · 158510.1080/15257770701548212 ↗
32. Lu C.-H. · Platform Sensing Biomol. · 2009 · 48 · 4785
33. Kanaori K. · Biochemistry · 2004 · 43 · 567210.1021/bi035419r ↗
34. Brazier J. A. · Angew. Chem., Int. Ed. · 2006 · 45 · 11410.1002/anie.200503110 ↗
35. Dai J. X. · J. Am. Chem. Soc. · 2009 · 131 · 610210.1021/ja900967r ↗
36. Leroy J. L. · Nucleic Acids Res. · 2009 · 37 · 412710.1093/nar/gkp340 ↗