Metal-base pairing in DNA

被引：203

作者：

Clever, Guido H. ^{[1
]}

Shionoya, Mitsuhiko ^{[1
]}

机构：

[1] Univ Tokyo, Dept Chem, Grad Sch Sci, Bunkyo Ku, Tokyo 1130033, Japan

来源：

COORDINATION CHEMISTRY REVIEWS | 2010年 / 254卷 / 19-20期

关键词：

DNA; Metal-base pair; Double strand; Nanoarchitecture; Metal stack; Hydroxypyridone; NUCLEIC-ACIDS; ELECTRON-TRANSFER; HG-II; MAGNETIC-INTERACTIONS; DUPLEX; IONS; NANOSCALE; OLIGONUCLEOTIDES; MERCURY(II); BINDING;

D O I：

10.1016/j.ccr.2010.04.014

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The use of DNA as a molecular wire in nanoscale electronic architectures would greatly benefit from its capability of sequence-specific self-assembly Although single electrons and positive charges have been shown to be transmitted by natural DNA over a distance of several base pans, the high ohmic resistance of unmodified oligonucleotides imposes a serious obstacle Exchanging some or all of the Watson-Crick base pairs in DNA by metal complexes may solve this problem and evolve DNA-like materials with superior conductivity for future nano-electronic applications The so-called metal-base pairs are formed from suitable transition metal ions and ligand-like nucleosides which are introduced into both of the two pairing strands by automated DNA synthesis This review illustrates the basic concepts of metal-base pairing and highlights recent developments in the field (C) 2010 Elsevier B V All rights reserved.

引用

页码：2391 / 2402

页数：12

共 100 条

[1] M-DNA:: A complex between divalent metal ions and DNA which behaves as a molecular wire [J].

Aich, P ;

Labiuk, SL ;

Tari, LW ;

Delbaere, LJT ;

Roesler, WJ ;

Falk, KJ ;

Steer, RP ;

Lee, JS .

JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (02) :477-485

[2] Assembling materials with DNA as the guide [J].

Aldaye, Faisal A. ;

Palmer, Alison L. ;

Sleiman, Hanadi F. .

SCIENCE, 2008, 321 (5897) :1795-1799

[3]

Aldaye FA, 2009, NAT NANOTECHNOL, V4, P349, DOI [10.1038/nnano.2009.72, 10.1038/NNANO.2009.72]

[4] Self-assembly of a nanoscale DNA box with a controllable lid [J].

Andersen, Ebbe S. ;

Dong, Mingdong ;

Nielsen, Morten M. ;

Jahn, Kasper ;

Subramani, Ramesh ;

Mamdouh, Wael ;

Golas, Monika M. ;

Sander, Bjoern ;

Stark, Holger ;

Oliveira, Cristiano L. P. ;

Pedersen, Jan Skov ;

Birkedal, Victoria ;

Besenbacher, Flemming ;

Gothelf, Kurt V. ;

Kjems, Jorgen .

NATURE, 2009, 459 (7243) :73-U75

[5]

[Anonymous], 1965, Electronics

[6] Structure of a copper-mediated base pair in DNA [J].

Atwell, S ;

Meggers, E ;

Spraggon, G ;

Schultz, PG .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (49) :12364-12367

[7] Understanding nucleic acids using synthetic chemistry [J].

Benner, SA .

ACCOUNTS OF CHEMICAL RESEARCH, 2004, 37 (10) :784-797

[8] Conformational change induced by metal-ion-binding to DNA containing the artificial 1,2,4-triazole nucleoside [J].

Bohme, Dominik ;

Dupre, Nicole ;

Megger, Dominik A. ;

Muller, Jens .

INORGANIC CHEMISTRY, 2007, 46 (24) :10114-10119

[9] Investigation of the pathways of excess electron transfer in DNA with flavin-donor and oxetane-acceptor modified DNA hairpins [J].

Breeger, Sascha ;

von Meltzer, Martin ;

Hennecke, Ulrich ;

Carell, Thomas .

CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (25) :6469-6477

[10] METAL ION-BIOMOLECULE INTERACTIONS .12. H-1 AND C-13 NMR EVIDENCE FOR THE PREFERRED REACTION OF THYMIDINE OVER GUANOSINE IN EXCHANGE AND COMPETITION REACTIONS WITH MERCURY(II) AND METHYLMERCURY(II) [J].

BUNCEL, E ;

BOONE, C ;

JOLY, H ;

KUMAR, R ;

NORRIS, AR .

JOURNAL OF INORGANIC BIOCHEMISTRY, 1985, 25 (01) :61-73

← 1 2 3 4 5 6 7 8 9 10 →