Direct measurement of lateral transport in membranes by using time-resolved spatial photometry.
Open Access
- 1 June 1985
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 82 (12) , 4122-4126
- https://doi.org/10.1073/pnas.82.12.4122
Abstract
Spatially resolving light detectors allow, with proper calibration, quantitative analysis of the variations in two-dimensional intensity distributions over time. An ultrasensitive microfluorometer was assembled by using as a detector a microchannel plate-intensified video camera. The camera was interfaced with a software-based digital video analysis system to digitize, average, and process images and to directly control the timing of the experiments to minimize exposure of the specimen to light. The detector system has been characterized to allow its use as a photometer. A major application has been to perform fluorescence recovery after photobleaching measurements by using the camera in place of a photomultiplier tube (video-FRAP) with the goal of detecting possible anisotropic diffusion or convective flow. Analysis of the data on macromolecular diffusion in homogenous aqueous glycol solutions yielded diffusion constants in agreement with previous measurements. Results on lipid probe diffusion in dimyristoylphosphatidylcholine multibilayers indicated that at temperatures above the gel-to-liquid crystalline phase transition diffusion is isotropic, and analysis of video-FRAP data yielded diffusion coefficients consistent with those measured previously by using spot photobleaching. However, lipid probes in these multibilayers held just below the main phase transition temperature exhibited markedly anisotropic diffusive fluxes when the bleaching beam was positioned proximate to domain boundaries in the P beta' phase. Lipid probes and lectin receptor complexes diffused isotropically in fibroblast surface membranes with little evidence for diffusion channeled parallel to stress fibers. A second application was to trace the time evolution of cell surface reactions such as patching. The feasibility of following, on the optical scale, the growth of individual receptor clusters induced by the ligand wheat germ agglutinin was demonstrated.This publication has 18 references indexed in Scilit:
- Digital imaging fluorescence microscopy: spatial heterogeneity of photobleaching rate constants in individual cells.The Journal of cell biology, 1985
- Distribution of hematoporphyrin derivative in the rat 9L gliosarcoma brain tumor analyzed by digital video fluorescence microscopyJournal of Neurosurgery, 1984
- Distribution of receptors and functions on cell surfaces: quantitation of ligand-receptor mobility and a new model for the control of plasma membrane topographyPhilosophical Transactions of the Royal Society of London. B, Biological Sciences, 1982
- Fibronectins: multifunctional modular glycoproteins.The Journal of cell biology, 1982
- Lipid lateral diffusion in the surface membrane of cells and in multibilayers formed from plasma membrane lipidsBiochemistry, 1981
- Local measurement of lateral motion in erythrocyte membranes by photobleaching techniqueBiochimica et Biophysica Acta (BBA) - Biomembranes, 1980
- The visualization of fluorescent proteins in living cells by video intensification microscopy (VIM)Cell, 1978
- Measurement of the translation mobility of concanavalin a in glycerol-saline solutions and on the cell surface by fluorescence recovery after photobleachingBiochimica et Biophysica Acta (BBA) - Biomembranes, 1976
- Measurement of the lateral mobility of cell surface components in single living cells by fluorescence recovery after photobleachingJournal of Supramolecular Structure, 1976
- A microfluorimetric study of translational diffusion in erythrocyte membranesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1974