Direct voltammetry of cytochrome c at trace concentrations with nanoelectrode ensembles

Gold nanoelectrode ensembles (NEEs) are prepared by electroless plating of Au nanoelectrode elements within the pores of a microporous polycarbonate template membrane. The surfaces of these NEEs and also the inner morphology of the gold nanofibers inside the membrane pores are imaged by scanning and transmission electron microscopy. The use of NEEs in micromolar cytochrome c (cyt c) solutions reveals the possibility of observing the direct electrochemistry of the protein, without the need of any promoter or mediator. Cyt c detection limits at NEEs are 1.0 μM by cyclic voltammetry and 0.03 μM by differential pulse voltammetry. The main difference between the voltammetric signals recorded at NEEs in the absence and in the presence of the promoter 4,4′-bipyridyl is the more extended dynamic range obtained in the latter case. Quartz crystal microbalance measurements at gold-coated quartz crystals show that, in the absence of promoter, adsorption problems are responsible for the poisoning of the electrode surface. Such adsorption is, however, concentration dependent, so that in diluted solutions (cyt c concentration ⩽20 μM) it becomes negligible. Experimental evidence indicates that the capability of NEEs to detect the direct electrochemistry of cyt c even in the absence of promoters is related to their peculiar property of furnishing well-resolved voltammetric signals in diluted solutions, where this unwanted adsorption is eliminated.

[1]  R. Crooks,et al.  Interactions between organized, surface-confined monolayers and vapor-phase probe molecules. 7. Comparison of self-assembling n-alkanethiol monolayers deposited on gold from liquid and vapor phases , 1993 .

[2]  Charles R. Martin,et al.  Electrochemistry of phenothiazine and methylviologen biosensor electron-transfer mediators at nanoelectrode ensembles , 2000 .

[3]  A. Bond,et al.  Relationship of two electroactive forms of horse heart cytochrome c at gold and glassy carbon electrodes in water and methanol , 1987 .

[4]  Jonathan M. Cooper,et al.  Direct electron transfer reactions between immobilized cytochrome c and modified gold electrodes , 1993 .

[5]  C. Brett,et al.  Electrochemical behaviour of cytochrome c at electrically heated microelectrodes. , 1999, Journal of pharmaceutical and biomedical analysis.

[6]  P. Ugo,et al.  Ionomer-coated electrodes and nanoelectrode ensembles as electrochemical environmental sensors: recent advances and prospects. , 2002, Chemphyschem : a European journal of chemical physics and physical chemistry.

[7]  P. Dobson,et al.  Electron transfer processes of redox proteins at inherently modified microelectrode array devices , 2000 .

[8]  Jan F. Chlebowski,et al.  Cyclic voltammetry and derivative cyclic voltabsorptometry of purified horse heart cytochrome c at tin-doped indium oxide optically transparent electrodes , 1982 .

[9]  A. Bond Chemical and electrochemical approaches to the investigation of redox reactions of simple electron transfer metalloproteins , 1994 .

[10]  J. Hart,et al.  Direct electrochemistry of cytochrome c at plain and membrane modified screen-printed carbon electrodes , 2001 .

[11]  Á. Szűcs,et al.  Stable and reversible electrochemistry of cytochrome c on bare electrodes Part II: Effects of experimental conditions , 1995 .

[12]  D. Walt,et al.  Fabrication of an optoelectrochemical microring array. , 2002, Analytical chemistry.

[13]  I. Taniguchi,et al.  722-The effect of pH on the temperature dependence of the redox potential of horse heart cytochrome c at a bis(4-pyridyl)disulfide-modified gold electrode , 1984 .

[14]  Rupert Huber,et al.  TEMPLATE SYNTHESIS OF NANOWIRES IN POROUS POLYCARBONATE MEMBRANES: ELECTROCHEMISTRY AND MORPHOLOGY , 1997 .

[15]  T. Cotton,et al.  An electrochemical approach to investigate gated electron transfer using a physiological model system: Cytochrome c immobilized on carboxylic acid-terminated alkanethiol self-assembled monolayers on gold electrodes , 2000 .

[16]  Redox reactions of heme-containing metalloproteins: dynamic effects of self-assembled monolayers on thermodynamics and kinetics of cytochrome c electron-transfer reactions , 2000 .

[17]  C. R. Martin,et al.  Template preparation of nanoelectrode ensembles. Achieving the ‘pure-radial’ electrochemical-response limiting case , 1996 .

[18]  M. Natan,et al.  MORPHOLOGY-DEPENDENT ELECTROCHEMISTRY OF CYTOCHROME C AT AU COLLOID-MODIFIED SNO2 ELECTRODES , 1996 .

[19]  A. Bond,et al.  A microscopic model of electron transfer at electroactive sites of molecular dimensions for reduction of cytochrome c at basal- and edge-plane graphite electrodes , 1989 .

[20]  J. Savéant,et al.  Charge transfer at partially blocked surfaces , 1983 .

[21]  F. M. Hawkridge,et al.  Temperature and electrolyte effects on the electron-transfer reactions of cytochrome c , 1985 .

[22]  C. R. Martin,et al.  Ultramicroelectrode ensembles. Comparison of experimental and theoretical responses and evaluation of electroanalytical detection limits , 1989 .

[23]  Katsumi Niwa,et al.  Redox reaction mechanism of cytochrome c at modified gold electrodes , 1990 .

[24]  V. Rotello,et al.  Fabrication and characterization of nanoelectrode arrays formed via block copolymer self-assembly , 2001 .

[25]  Henry N. Blount,et al.  Interfacial electrochemistry of cytochrome c at tin oxide, indium oxide, gold, and platinum electrodes , 1984 .

[26]  Stanley Bruckenstein,et al.  Experimental aspects of use of the quartz crystal microbalance in solution , 1985 .

[27]  Á. Szűcs,et al.  Stable and reversible electrochemistry of cytochrome c on bare electrodes Part 1. Effect of ionic strength , 1995 .

[28]  I. Rubinstein,et al.  Organized self-assembling monolayers on electrodes. 2. Monolayer-based ultramicroelectrodes for the study of very rapid electrode kinetics , 1987 .

[29]  H. Hill,et al.  Novel method for the investigation of the electrochemistry of metalloproteins: cytochrome c , 1977 .

[30]  Nicholas J. Walton,et al.  Surface modifiers for the promotion of direct electrochemistry of cytochrome c , 1984 .

[31]  Frieder W. Scheller,et al.  Electrochemistry of Cytochrome c Immobilized on Colloidal Gold Modified Carbon Paste Electrodes and Its Electrocatalytic Activity , 2002 .

[32]  Isao Taniguchi,et al.  Reversible electrochemical reduction and oxidation of cytochrome c at a bis(4-pyridyl) disulphide-modified gold electrode , 1982 .

[33]  N. Giordano,et al.  Fabrication of 80 Å metal wires , 1984 .

[34]  V. Massey The microestimation of succinate and the extinction coefficient of cytochrome c. , 1959, Biochimica et biophysica acta.

[35]  R. Compton,et al.  Voltammetry in the Presence of Ultrasound: Sonovoltammetric Detection of Cytochrome c under Very Fast Mass Transport Conditions , 1996 .

[36]  George E. Possin,et al.  A method for forming very small diameter wires (Notes) , 1970 .

[37]  Á. Szűcs,et al.  Ellipsometry of cytochrome c on gold surfaces: effect of 4,4′-dipyridyl disulfide , 1992 .

[38]  G. Che,et al.  Molecular recognition based on (3-mercaptopropyl) trimethoxysilane modified gold electrodes , 1996 .

[39]  Charles R. Martin,et al.  FABRICATION AND EVALUATION OF NANOELECTRODE ENSEMBLES , 1995 .

[40]  P. Hildebrandt,et al.  Cytochrome c at charged interfaces. 1. Conformational and redox equilibria at the electrode/electrolyte interface probed by surface-enhanced resonance Raman spectroscopy. , 1989, Biochemistry.

[41]  E. Lojou,et al.  Poly(ester-sulfonic acid) : modified carbon electrodes for the electrochemical study of c-type cytochromes , 1999 .

[42]  P. Ugo,et al.  Ion-exchange voltammetry and electrocatalytic sensing capabilities of cytochrome c at polyestersulfonated ionomer coated glassy carbon electrodes. , 2002, Biosensors & bioelectronics.

[43]  V. Menon,et al.  Ion-exchange voltammetry at polymer film-coated nanoelectrode ensembles. , 1996, Analytical chemistry.

[44]  H. Hill,et al.  Electrochemistry of horse heart cytochrome c , 1979 .

[45]  Takamasa Sagara,et al.  Spectroelectrochemical study of the redox reaction mechanism of cytochrome c at a gold electrode in a neutral solution in the presence of 4,4'-bipyridyl as a surface modifier , 1991 .

[46]  A. Bond,et al.  Interpretation of the electrochemistry of cytochrome c at macro and micro sized carbon electrodes using a microscopic model based on a partially blocke , 1991 .