Direct electron transfer of glucose oxidase on carbon nanotubes

被引:493
作者
Guiseppi-Elie, A
Lei, CH
Baughman, RH
机构
[1] Virginia Commonwealth Univ, Dept Chem Engn, Richmond, VA 23284 USA
[2] Virginia Commonwealth Univ, Ctr Bioelect Biosensors & Biochips, Richmond, VA 23284 USA
[3] Honeywell Corp, Res Technol Ctr, Morristown, NJ 07962 USA
关键词
D O I
10.1088/0957-4484/13/5/303
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this report, exploitation of the unique properties of single-walled carbon nanotubes (SWNT) leads to the achievement of direct electron transfer with the redox active centres of adsorbed oxidoreductase enzymes. Flavin adenine dinucleotide (FAD), the redox active prosthetic group of flavoenzymes that catalyses important biological redox reactions and the flavoenzyme glucose oxidase (GOx), were both found to spontaneously adsorb onto carbon nanotube bundles. Both FAD and GOx were found to spontaneously adsorb to unannealed carbon nanotubes that were cast onto glassy carbon electrodes and to display quasi-reversible one-electron transfer. Similarly, GOx was found to spontaneously adsorb to annealed, single-walled carbon nanotube paper and to display quasi-reversible one-electron transfer. In particular, GOx immobilized in this way was shown, in the presence of glucose, to maintain its substrate-specific enzyme activity. It is believed that the tubular fibrils become positioned within tunnelling distance of the cofactors with little consequence to denaturation. The combination of SWNT with redox active enzymes would appear to offer an excellent and convenient platform for a fundamental understanding of biological redox reactions as well as the development of reagentless biosensors and nanobiosensors.
引用
收藏
页码:559 / 564
页数:6
相关论文
共 23 条
[1]  
Balavoine F, 1999, ANGEW CHEM INT EDIT, V38, P1912, DOI 10.1002/(SICI)1521-3773(19990712)38:13/14<1912::AID-ANIE1912>3.0.CO
[2]  
2-2
[3]   Carbon nanotube actuators [J].
Baughman, RH ;
Cui, CX ;
Zakhidov, AA ;
Iqbal, Z ;
Barisci, JN ;
Spinks, GM ;
Wallace, GG ;
Mazzoldi, A ;
De Rossi, D ;
Rinzler, AG ;
Jaschinski, O ;
Roth, S ;
Kertesz, M .
SCIENCE, 1999, 284 (5418) :1340-1344
[4]   Multiprobe transport experiments on individual single-wall carbon nanotubes [J].
Bezryadin, A ;
Verschueren, ARM ;
Tans, SJ ;
Dekker, C .
PHYSICAL REVIEW LETTERS, 1998, 80 (18) :4036-4039
[5]   Noncovalent sidewall functionalization of single-walled carbon nanotubes for protein immobilization [J].
Chen, RJ ;
Zhang, YG ;
Wang, DW ;
Dai, HJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (16) :3838-3839
[6]   FULLY COLLAPSED CARBON NANOTUBES [J].
CHOPRA, NG ;
BENEDICT, LX ;
CRESPI, VH ;
COHEN, ML ;
LOUIE, SG ;
ZETTL, A .
NATURE, 1995, 377 (6545) :135-138
[7]   The immobilisation of proteins in carbon nanotubes [J].
Davis, JJ ;
Green, MLH ;
Hill, HAO ;
Leung, YC ;
Sadler, PJ ;
Sloan, J ;
Xavier, AV ;
Tsang, SC .
INORGANICA CHIMICA ACTA, 1998, 272 (1-2) :261-266
[8]  
Dong LW, 1996, J MOL RECOGNIT, V9, P383, DOI 10.1002/(SICI)1099-1352(199634/12)9:5/6<383::AID-JMR269>3.0.CO
[9]  
2-Z
[10]  
Dryhurst G, 1982, BIOL ELECTROCHEMISTR