Evaluation of diffusion coefficient of P-glycoprotein molecules labeled with green fluorescent protein in living cell

Xuan Hoa Vu1, Nguyen Dac Dien2, Thi Thu Ha Pham3

  • 1Institute of Science and Technology, TNU- University of Sciences (TNUS), Tan Thinh ward, Thai Nguyen city, Viet Nam.

Insights

Single Particle Tracking (SPT) and Total Internal Reflection Fluorescence Microscopy (TIRFM) visualize P-glycoprotein (PGP) dynamics in living cell membranes. This reveals molecular movement and cell environment heterogeneity, aiding cancer drug resistance research.

Area of Science:

  • Cell biology
  • Biophysics
  • Molecular dynamics

Background:

  • Metastatic cancers require chemotherapy, but cancer cells develop multidrug resistance.
  • P-glycoprotein (PGP) is a key factor in multidrug resistance, studied for decades.
  • Advances in microscopy enable visualization of single molecules in living cells.

Purpose of the Study:

  • To characterize the dynamics of individual P-glycoprotein (PGP) molecules in living cell membranes.
  • To utilize Total Internal Reflection Fluorescence Microscopy (TIRFM) for single-molecule analysis.
  • To understand single-molecule features and diffusion kinetics of membrane-bound molecules.

Main Methods:

  • Labeling P-glycoproteins (PGP) with green fluorescent protein (GFP) in Madin-Darby canine kidney (MDCK) cells.
  • Employing Total Internal Reflection Fluorescence Microscopy (TIRFM) to monitor GFP-PGP dynamics.
  • Analyzing single fluorescent spots to obtain diffusion maps and kinetic parameters.

Main Results:

  • High-resolution images and diffusion maps of membrane proteins on cell surfaces were obtained.
  • Local diffusion properties of specific proteins on single cells were characterized.
  • Diffusion coefficient, mean square displacement, average velocity, and cell environment heterogeneity were determined.

Conclusions:

  • TIRFM allows detailed characterization of individual membrane protein dynamics in living cells.
  • Understanding PGP molecule movement provides insights into multidrug resistance mechanisms.
  • This approach enhances the study of molecular behavior within the complex cellular environment.