DNA electron transfer processes: Some theoretical notions

被引:114
作者
Berlin, YA
Kurnikov, IV
Beratan, D
Ratner, MA
Burin, AL
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Ctr Nanofabricat & Mol Self Assembly, Evanston, IL 60208 USA
[3] Northwestern Univ, Mat Res Ctr, Evanston, IL 60208 USA
[4] Duke Univ, Dept Chem, Durham, NC 27708 USA
[5] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
来源
LONG-RANGE CHARGE TRANSFER IN DNA II | 2004年 / 237卷
关键词
electron transfer; hole transport; hopping; superexchange; coupling to the molecular surroundings;
D O I
10.1007/b94471
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge motion within DNA stacks, probed by measurements of electric conductivity and by time-resolved and steady-state damage yield measurements, is determined by a complex mixture of electronic effects, coupling to quantum and classical degrees of freedom of the atomic motions in the bath, and the effects of static and dynamic disorder. The resulting phenomena are complex, and probably cannot be understood using a single integrated modeling viewpoint. We discuss aspects of the electronic structure and overlap among base pairs, the viability of simple electronic structure models including tight-binding band pictures, and the Condon approximation for electronic mixing. We also discuss the general effects of disorder and environmental coupling, resulting in motion that can span from the coherent regime through superexchange-type hopping to diffusion and gated transport. Comparison with experiment can be used to develop an effective phenomenological multiple-site hopping/superexchange model, but the microscopic understanding of the actual behaviors is not yet complete.
引用
收藏
页码:1 / 36
页数:36
相关论文
共 105 条
[81]   ELECTRON-TRANSFER IN DNA - PREDICTIONS OF EXPONENTIAL-GROWTH AND DECAY OF COUPLING WITH DONOR-ACCEPTOR DISTANCE [J].
RISSER, SM ;
BERATAN, DN ;
MEADE, TJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (06) :2508-2510
[82]  
Schiff L. I., 1968, QUANTUM MECH
[83]   Long-range charge transfer in DNA: Transient structural distortions control the distance dependence [J].
Schuster, GB .
ACCOUNTS OF CHEMICAL RESEARCH, 2000, 33 (04) :253-260
[84]   Estimate of the reorganization energy for charge transfer in DNA [J].
Siriwong, K ;
Voityuk, AA ;
Newton, MD ;
Rösch, N .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (11) :2595-2601
[85]   Insulating behavior for DNA molecules between nanoelectrodes at the 100 nm length scale [J].
Storm, AJ ;
van Noort, J ;
de Vries, S ;
Dekker, C .
APPLIED PHYSICS LETTERS, 2001, 79 (23) :3881-3883
[86]   SOLITON EXCITATIONS IN POLYACETYLENE [J].
SU, WP ;
SCHRIEFFER, JR ;
HEEGER, AJ .
PHYSICAL REVIEW B, 1980, 22 (04) :2099-2111
[87]   Theoretical studies of GC-specific photocleavage of DNA via electron transfer: Significant lowering of ionization potential and 5'-localization of HOMO of stacked GG bases in B-form DNA [J].
Sugiyama, H ;
Saito, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (30) :7063-7068
[88]   The DNA-mediated formation of supramolecular mono- and multilayered nanoparticle structures [J].
Taton, TA ;
Mucic, RC ;
Mirkin, CA ;
Letsinger, RL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (26) :6305-6306
[89]   Distance dependence of electron transfer in DNA: The role of the reorganization energy and free energy [J].
Tavernier, HL ;
Fayer, MD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (48) :11541-11550
[90]   Tunneling energy effects on GC oxidation in DNA [J].
Tong, GSM ;
Kurnikov, IV ;
Beratan, DN .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (09) :2381-2392