Measuring Phagosomal pH by Fluorescence Microscopy

Methods Mol Biol. 2023:2692:153-169. doi: 10.1007/978-1-0716-3338-0_11.

Abstract

Dual-wavelength and dual-fluorophore ratiometric imaging has become a powerful tool for the study of pH in intracellular compartments. It allows for the dynamic imaging of live cells while accounting for changes in the focal plane, differential loading of the fluorescent probe, and photobleaching caused by repeated image acquisitions. Ratiometric microscopic imaging has the added advantage over whole-population methods of being able to resolve individual cells and even individual organelles. In this chapter, we provide a detailed discussion of the basic principles of ratiometric imaging and its application to the measurement of phagosomal pH, including probe selection, the necessary instrumentation, and calibration methods.

Keywords: CypHer5e; Dual-fluorophore ratio imaging; Dual-wavelength ratio imaging; Fluorescein; Fluorescence microscopy; Oregon Green; Phagosome; SNARF1; pH; pHrodo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fluorescent Dyes*
  • Hydrogen-Ion Concentration
  • Ionophores
  • Microscopy, Fluorescence / methods
  • Phagosomes*
  • Spectrometry, Fluorescence

Substances

  • Fluorescent Dyes
  • Ionophores