Silver-Mediated Double Helix: Structural Parameters for a Robust DNA Building Block

被引:23
作者
Chen, Xi [1 ]
Karpenko, Alexander [1 ]
Lopez-Acevedo, Olga [1 ,2 ]
机构
[1] Aalto Univ, COMP Ctr Excellence, Dept Appl Phys, POB 11100, Aalto 00076, Finland
[2] Univ Medellin, Fac Ciencias Basicas, Carrera 87 30-65, Medellin 050026, Colombia
基金
芬兰科学院;
关键词
SILVER(I)-MEDIATED BASE-PAIR; NUCLEIC-ACIDS; FORCE-FIELD; SIMULATION; CRYSTAL; SHAPES;
D O I
10.1021/acsomega.7b01089
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The DNA double helix is a versatile building block used in DNA nanotechnology. To potentiate the discovery of new DNA nanoscale assemblies, recently, silver cations have been introduced to pair DNA strands by base-Ag+-base bonding rather than by Watson-Crick pairing. In this work, we study the classical dynamics of a parallel silvermediated homobase double helix and compare it to the dynamics of the antiparallel double helix. Our classical simulations show that only the parallel double helix is highly stable through the 100 ns simulation time. A new type of Hbond previously proposed by our collaboration and recently observed in crystal-determined helices drives the physicochemical stabilization. Compared to the natural B-DNA form, the metal-mediated helix has a contracted axial base pair rise and smaller numbers of base pairs per turn. These results open the path for the inclusion of this robust metal-mediated building block into new nanoscale DNA assemblies.
引用
收藏
页码:7343 / 7348
页数:6
相关论文
共 50 条
[1]  
[Anonymous], 2002, ENCY LIFE SCI, DOI [DOI 10.1038/MPG.ELS.0003122, 10.1038/mpg.els.0003122]
[2]   DNA nanomachines [J].
Bath, Jonathan ;
Turberfield, Andrew J. .
NATURE NANOTECHNOLOGY, 2007, 2 (05) :275-284
[3]   A WELL-BEHAVED ELECTROSTATIC POTENTIAL BASED METHOD USING CHARGE RESTRAINTS FOR DERIVING ATOMIC CHARGES - THE RESP MODEL [J].
BAYLY, CI ;
CIEPLAK, P ;
CORNELL, WD ;
KOLLMAN, PA .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (40) :10269-10280
[4]   DNA-protected silver emitters: charge dependent switching of fluorescence [J].
Berdakin, Matias ;
Taccone, Martin I. ;
Pino, Gustavo A. ;
Sanchez, Cristian G. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2017, 19 (08) :5721-5726
[5]   The Amber biomolecular simulation programs [J].
Case, DA ;
Cheatham, TE ;
Darden, T ;
Gohlke, H ;
Luo, R ;
Merz, KM ;
Onufriev, A ;
Simmerling, C ;
Wang, B ;
Woods, RJ .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2005, 26 (16) :1668-1688
[6]   Linear response time-dependent density functional theory for van der Waals coefficients [J].
Chu, X ;
Dalgarno, A .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (09) :4083-4088
[7]   Metal-base pairing in DNA [J].
Clever, Guido H. ;
Shionoya, Mitsuhiko .
COORDINATION CHEMISTRY REVIEWS, 2010, 254 (19-20) :2391-2402
[8]   A 2ND GENERATION FORCE-FIELD FOR THE SIMULATION OF PROTEINS, NUCLEIC-ACIDS, AND ORGANIC-MOLECULES [J].
CORNELL, WD ;
CIEPLAK, P ;
BAYLY, CI ;
GOULD, IR ;
MERZ, KM ;
FERGUSON, DM ;
SPELLMEYER, DC ;
FOX, T ;
CALDWELL, JW ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (19) :5179-5197
[9]   Rapid prototyping of 3D DNA-origami shapes with caDNAno [J].
Douglas, Shawn M. ;
Marblestone, Adam H. ;
Teerapittayanon, Surat ;
Vazquez, Alejandro ;
Church, George M. ;
Shih, William M. .
NUCLEIC ACIDS RESEARCH, 2009, 37 (15) :5001-5006
[10]   Self-assembly of DNA into nanoscale three-dimensional shapes [J].
Douglas, Shawn M. ;
Dietz, Hendrik ;
Liedl, Tim ;
Hoegberg, Bjoern ;
Graf, Franziska ;
Shih, William M. .
NATURE, 2009, 459 (7245) :414-418