Surface-Enhanced Resonance Raman Spectroscopy Signals from Single Myoglobin Molecules

The extremely large cross-section available from metallic surface enhancement has been exploited to investigate the Raman spectrum of heme myoglobin adsorbed on silver colloidal nanoparticles at very low concentrations. The study has been performed on particles both in solution and immobilized onto a polymer-coated glass surface. In both the cases, we have observed striking temporal fluctuations in the surface-enhanced resonance Raman spectroscopy (SERRS) spectra collected at short times. A statistical analysis of the temporal intensity fluctuations and of the associated correlations of the Raman signals has allowed us to verify that the single molecule limit is approached. The possible connections of these fluctuations with the entanglement of the biomolecule within the local minima of its rough energy landscape is discussed.

[1]  R. Dasari,et al.  Ultrasensitive chemical analysis by Raman spectroscopy. , 1999, Chemical reviews.

[2]  S. Simon,et al.  Tracking single proteins within cells. , 2000, Biophysical journal.

[3]  C. Seidel,et al.  Homogeneity, transport and signal properties of single Ag particles studied by single-molecule surface-enhanced resonance Raman scattering. , 2001 .

[4]  S. Cannistraro,et al.  Solvent modulation of the structural heterogeneity in FeIII myoglobin samples: a low temperature EPR investigation , 2004, European Biophysics Journal.

[5]  N. F. Hulst,et al.  Analysis of individual (macro)molecules and proteins using near-field optics , 2000 .

[6]  G. Loppnow,et al.  EXCITED-STATE CHARGE-TRANSFER DYNAMICS OF AZURIN, A BLUE COPPER PROTEIN, FROM RESONANCE RAMAN INTENSITIES , 1997 .

[7]  M. Natan,et al.  Self-Assembled Metal Colloid Monolayers: An Approach to SERS Substrates , 1995, Science.

[8]  S. Cannistraro,et al.  Intensity fluctuations of the copper site resonant vibrational modes as observed by MD simulation in single plastocyanin molecule , 2001 .

[9]  M. Brunori,et al.  Enzyme Proteins. (Book Reviews: Hemoglobin and Myoglobin in Their Reactions with Ligands) , 1971 .

[10]  Thomas G. Spiro,et al.  Assignment of Protoheme Resonance Raman Spectrum by Heme Labeling in Myoglobin , 1996 .

[11]  N. F. van Hulst,et al.  Time-varying triplet state lifetimes of single molecules , 1999 .

[12]  S. Nie,et al.  Single-Molecule and Single-Nanoparticle SERS: Examining the Roles of Surface Active Sites and Chemical Enhancement , 2002 .

[13]  G. A. Blab,et al.  Autofluorescent proteins in single-molecule research: applications to live cell imaging microscopy. , 2001, Biophysical journal.

[14]  Ramasamy Manoharan,et al.  Detection and identification of a single DNA base molecule using surface-enhanced Raman scattering (SERS) , 1998 .

[15]  Hongxing Xu,et al.  Spectroscopy of Single Hemoglobin Molecules by Surface Enhanced Raman Scattering , 1999 .

[16]  M. Moskovits Surface-enhanced spectroscopy , 1985 .

[17]  Gilad Haran,et al.  Time-Dependent Single-Molecule Raman Scattering as a Probe of Surface Dynamics , 2001 .

[18]  Steven R. Emory,et al.  Probing Single Molecules and Single Nanoparticles by Surface-Enhanced Raman Scattering , 1997, Science.

[19]  H. Frauenfelder,et al.  Conformational substates in proteins. , 1988, Annual review of biophysics and biophysical chemistry.

[20]  D. Meisel,et al.  Adsorption and surface-enhanced Raman of dyes on silver and gold sols , 1982 .

[21]  Louis E. Brus,et al.  Ag Nanocrystal Junctions as the Site for Surface-Enhanced Raman Scattering of Single Rhodamine 6G Molecules , 2000 .

[22]  Mikael Käll,et al.  Single-molecule surface-enhanced Raman and fluorescence correlation spectroscopy of horseradish peroxidase , 2002 .

[23]  Louis E. Brus,et al.  Surface Enhanced Raman Spectroscopy of Individual Rhodamine 6G Molecules on Large Ag Nanocrystals , 1999 .

[24]  R. Dasari,et al.  Single Molecule Detection Using Surface-Enhanced Raman Scattering (SERS) , 1997 .

[25]  Champion,et al.  Spectral broadening in biomolecules. , 1986, Physical review letters.