Proteins in action monitored by time-resolved FTIR spectroscopy

Chemphyschem. 2005 May;6(5):881-8. doi: 10.1002/cphc.200400504.

Abstract

In the post genome era proteins coming into the focus of life sciences. X-ray structure analysis and NMR spectroscopy are established methods to determine the geometry of proteins. In order to determine the molecular reaction mechanism of proteins, time-resolved FTIR (trFTIR) difference spectroscopy emerges as a valuable tool. In this Minireview we describe the trFTIR difference spectroscopy and show its application on the light-driven proton pump bacteriorhodopsin (bR), the photosynthetic reaction center and the GTPase Ras, which is crucial in signal transduction. The main principles of the technique are presented, including a summary of triggering techniques, scan modes and analysis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bacteriorhodopsins / chemistry*
  • GTP Phosphohydrolases / chemistry
  • Hydrogen Bonding
  • Kinetics
  • Light
  • Magnetic Resonance Spectroscopy / methods*
  • Models, Chemical
  • Models, Molecular
  • Models, Statistical
  • Molecular Conformation
  • Protein Conformation
  • Proteins / chemistry
  • Signal Transduction
  • Spectrophotometry
  • Spectrophotometry, Infrared
  • Spectroscopy, Fourier Transform Infrared / methods*
  • Time Factors
  • X-Rays

Substances

  • Proteins
  • Bacteriorhodopsins
  • GTP Phosphohydrolases