Mechanisms for the Direct Electron Transfer of Cytochrome c Induced by Multi-Walled Carbon Nanotubes

Multi-walled carbon nanotube (MWCNT)-modified electrodes can promote the direct electron transfer (DET) of cytochrome c (Cyt c). There are several possible mechanisms that explain the DET of Cyt c. In this study, several experimental methods, including Fourier transform infrared spectroscopy, circular dichroism, ultraviolet-visible absorption spectroscopy, and electron paramagnetic resonance spectroscopy were utilized to investigate the conformational changes of Cyt c induced by MWCNTs. The DET mechanism was demonstrated at various nano-levels: secondary structure, spatial orientation, and spin state. In the presence of MWCNTs, the secondary structure of Cyt c changes, which exposes the active site, then, the orientation of the heme is optimized, revolving the exposed active center to the optimum spatial orientation for DET; and finally, a transition of spin states is induced, providing relatively high energy and a more open microenvironment for electron transfer. These changes at different nano-levels are closely connected and form a complex process that promotes the electron transfer of Cyt c.

[1]  Abhay Vaze,et al.  Biocatalytic anode for glucose oxidation utilizing carbon nanotubes for direct electron transfer with glucose oxidase. , 2009, Electrochemistry communications.

[2]  Jing-Yuan Wang,et al.  Carbon nanotubes as electrode modifier promoting direct electron transfer from Shewanella oneidensis. , 2010, Biosensors & bioelectronics.

[3]  Richard J. Coles,et al.  Protein electrochemistry at carbon nanotube electrodes , 1997 .

[4]  Isao Taniguchi,et al.  The Direct Electron Transfer Reactions of Cytochrome c at Electrode Surfaces , 1995 .

[5]  Ji Liang,et al.  Electrocatalytic Reduction of Nitrite Using a Carbon Nanotube Electrode in the Presence of Cupric Ions , 2004 .

[6]  S. Sligar,et al.  Coupling of spin, substrate, and redox equilibria in cytochrome P450. , 1976, Biochemistry.

[7]  T. Rush,et al.  IR spectra of cytochrome c denatured with deuterated guanidine hydrochloride show increase in beta sheet. , 2003, Biopolymers.

[8]  Zhihui Dai,et al.  Direct electron transfer of cytochrome c immobilized on a NaY zeolite matrix and its application in biosensing , 2004 .

[9]  Hermas R. Jiménez,et al.  Protein Unfolding: 1H‐NMR Studies of Paramagnetic Ferricytochrome c‐550 from Horse Heart , 2005 .

[10]  Arunas Ramanavicius,et al.  Hemoproteins in Design of Biofuel Cells , 2009 .

[11]  Shaojun Dong,et al.  pH-dependent conformational changes of ferricytochrome c induced by electrode surface microstructure. , 2004, Biophysical chemistry.

[12]  J Turner,et al.  Coupled electron-transfer and spin-exchange reactions , 2001 .

[13]  A. Hagarman,et al.  The conformational manifold of ferricytochrome c explored by visible and far-UV electronic circular dichroism spectroscopy. , 2008, Biochemistry.

[14]  Jingbo Hu,et al.  Direct Electrochemistry and Electrocatalysis of Myoglobin Immobilized on Gold Nanoparticles/Carbon Nanotubes Nanohybrid Film , 2008 .

[15]  A. Salimi,et al.  Direct electrochemistry and electrocatalytic activity of catalase incorporated onto multiwall carbon nanotubes-modified glassy carbon electrode. , 2005, Analytical biochemistry.

[16]  Y H Chen,et al.  Determination of the secondary structures of proteins by circular dichroism and optical rotatory dispersion. , 1972, Biochemistry.

[17]  J. Gaillard,et al.  Electron transfer across the O2- generating flavocytochrome b of neutrophils. Evidence for a transition from a low-spin state to a high-spin state of the heme iron component. , 1996, Biochemistry.

[18]  J. Justin Gooding,et al.  Achieving Direct Electrical Connection to Glucose Oxidase Using Aligned Single Walled Carbon Nanotube Arrays , 2005 .

[19]  Andreas Offenhäusser,et al.  Electrochemical characterization of the effect of gold nanoparticles on the electron transfer of cytochrome c , 2009 .

[20]  J L Hoard,et al.  Stereochemistry of hemes and other metalloporphyrins. , 1971, Science.

[21]  Qi-long Li,et al.  Studies on electrochemical behaviour of cephalexin , 1993 .

[22]  Ray H. Baughman,et al.  Direct electron transfer of glucose oxidase on carbon nanotubes , 2002 .

[23]  Ulrich Zerweck,et al.  The effect of molecular orientation on the potential of porphyrin-metal contacts. , 2008, Nano letters.

[24]  P. George,et al.  A spectrophotometric study of ionizations in methaemoglobin. , 1953, The Biochemical journal.

[25]  K. Vengatajalabathy Gobi,et al.  Efficient mediatorless superoxide sensors using cytochrome c-modified electrodes : surface nano-organization for selectivity and controlled peroxidase activity , 2000 .

[26]  Jing Li,et al.  The direct electrochemistry behavior of Cyt c on the modified glassy carbon electrode by SBA-15 with a high-redox potential , 2008 .

[27]  Steven S Saavedra,et al.  Adsorptive immobilization of cytochrome c on indium/tin oxide (ITO): electrochemical evidence for electron transfer-induced conformational changes , 2002 .

[28]  Zhonghua Lin,et al.  Time-resolved UV-vis spectroelectrochemical studies of the electron transfer process of cytochrome c , 2000 .

[29]  Jing-Juan Xu,et al.  Direct electrochemistry and electrocatalysis of heme proteins immobilized on gold nanoparticles stabilized by chitosan. , 2005, Analytical biochemistry.

[30]  Ping Wu,et al.  Immobilization and direct electrochemistry of cytochrome c at a single-walled carbon nanotube-modified electrode , 2006 .

[31]  Thomas G. Spiro,et al.  A conformational switch to beta-sheet structure in cytochrome c leads to heme exposure. Implications for cardiolipin peroxidation and apoptosis. , 2007, Journal of the American Chemical Society.

[32]  Ping Wu,et al.  Direct Electrochemistry and Bioelectrocatalysis of Myoglobin at a Carbon Nanotube-Modified Electrode , 2007 .

[33]  Zifeng Deng,et al.  Morphology-dependent electrochemistry and electrocatalytical activity of cytochrome c. , 2007, Langmuir : the ACS journal of surfaces and colloids.

[34]  C. Hackenbrock,et al.  Multiple conformations of physiological membrane-bound cytochrome c. , 1998, Biochemistry.

[35]  Shaojun Dong,et al.  Effect of electrode surface microstructure on electron transfer induced conformation changes in cytochrome c monitored by in situ UV and CD spectroelectrochemistry. , 2005, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[36]  Hua-Zhang Zhao,et al.  Direct electron transfer and conformational change of glucose oxidase on carbon nanotube-based electrodes , 2010 .

[37]  Zhennan Gu,et al.  Direct electrochemistry of cytochrome c at a glassy carbon electrode modified with single-wall carbon nanotubes. , 2002, Analytical chemistry.

[38]  B. A. Kuznetsov,et al.  The effect of the orientation of cytochrome c molecules covalently attached to the electrode surface upon their electrochemical activity , 1994 .

[39]  Yufeng Zheng,et al.  Electrochemistry of bilirubin oxidase at carbon nanotubes , 2010 .

[40]  Dusan Losic,et al.  Protein electrochemistry using aligned carbon nanotube arrays. , 2003, Journal of the American Chemical Society.

[41]  H. Mantsch,et al.  The use and misuse of FTIR spectroscopy in the determination of protein structure. , 1995, Critical reviews in biochemistry and molecular biology.

[42]  M. Fabian,et al.  Influence of NaCl and sorbitol on the stability of conformations of cytochrome c. , 2008, Biophysical chemistry.

[43]  An Xue,et al.  A novel layer-by-layer self-assembled carbon nanotube-based anode: Preparation, characterization, and application in microbial fuel cell , 2010 .

[44]  M. Perutz Stereochemistry of cooperative effects in haemoglobin. , 1970, Nature.

[45]  Kohei Uosaki,et al.  Electrochemistry of cytochrome c. Comparison of the electron transfer at a surface-modified gold electrode with that to cytochrome oxidase , 1979 .

[46]  Li Zhang,et al.  Direct electrochemistry of cytochrome c on a multi-walled carbon nanotubes modified electrode and its electrocatalytic activity for the reduction of H2O2 , 2005 .