Resonance Raman microspectroscopy of myeloperoxidase and cytochrome b558 in human neutrophilic granulocytes

Biophys J. 1998 Jun;74(6):3250-5. doi: 10.1016/S0006-3495(98)78031-2.

Abstract

With (resonance) Raman microscospectroscopy, it is possible to investigate the chemical constitution of a very small volume (0.5 fl) in a living cell. We have measured resonance Raman spectra in the cytoplasm of living normal, myeloperoxidase (MPO)-deficient, and cytochrome b558-deficient neutrophils and in isolated specific and azurophilic granule fractions, using an excitation wavelength of 413.1 nm. Similar experiments were performed after reduction of the redox centers by the addition of sodium dithionite. The specific and azurophilic granules in both redox states appeared to have clearly distinguishable Raman spectra when exciting at a wavelength of 413.1 nm. The azurophilic granules and the cytochrome b558-deficient neutrophils showed Raman spectra similar to that of the isolated MPO. The spectra of the specific granules and the MPO-deficient neutrophils corresponded very well to published cytochrome b558 spectra. The resonance Raman spectrum of the cytoplasmic region of normal neutrophilic granulocytes could be fitted with a combination of the spectra of the specific and azurophilic granules, which shows that the Raman signal of neutrophilic granulocytes mainly originates from MPO and cytochrome b558, at an excitation wavelength of 413.1 nm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytochrome b Group / blood*
  • Cytochrome b Group / deficiency
  • Cytoplasmic Granules / metabolism
  • Humans
  • In Vitro Techniques
  • Microchemistry
  • NADPH Oxidases*
  • Neutrophils / metabolism*
  • Peroxidase / blood*
  • Peroxidase / deficiency
  • Sensitivity and Specificity
  • Spectrum Analysis, Raman / instrumentation
  • Spectrum Analysis, Raman / methods

Substances

  • Cytochrome b Group
  • cytochrome b558
  • Peroxidase
  • NADPH Oxidases