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From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope
Published on: October 9, 2014
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.
Abstract:
The movement of individual molecules inside living cells has recently been resolved by single particles tracking (SPT) method which is a powerful tool for probing the organization and dynamics of the plasma membrane constituents. Effective treatment of metastatic cancers requires the toxic chemotherapy, however this therapy leads to the multidrug resistance phenomenon of the cancer cells, in which the cancer cells resist simultaneously to different drugs with different targets and chemical structures. P-glycoprotein molecules which are responsible for multidrug resistance of many cancer cells have been studied by cancer biologists during past haft of century. Recently, advances in laser and detector technologies have enabled single fluorophores to be visualized in aqueous solution. The development of the total internal reflection fluorescent microscope (TIRFM) provided means to monitor dynamic molecular localization in living cells. In this paper, P-glycoproteins (PGP) were labeled with green fluorescent protein (GFP) in living cell membrane of Madin-Darby canine kidney (MDCK) and the TIRFM method was used to characterize the dynamics of individual protein molecules on the surface of living cells. An evanescent field was produced by a totally internally reflected and a laser beam was illuminated the glass-water interface. GFP-PGP proteins that entered the evanescent field appeared as individual spots of light which were slighter than background fluorescence. We obtained high-resolution images and diffusion maps of membrane proteins on cell surface and showed the local diffusion properties of specific proteins on single cells. We also determined the diffusion coefficient, the mean square displacement and the average velocity of the tracked particles, as well as the heterogeneity of the cell environment. This study enabled us to understand single-molecule features in living cell and measure the diffusion kinetics of membrane-bound molecules.
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.
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