INTERNATIONAL INSTITUTE OF BIOPHYSICS
Conference on Biophotons 1999
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THE LOW FREQUENCY COHERENT ACTIVITY IN LIVING CELLS

V.P.Tychinsky*, T. Vyshenskaja, and D. G. Weiss+

*Moscow State Institute for Radioengineering, Electronics and Automation, Vernadskii Pr. 78, Moscow 117454, Russia, Moscow State University, Phys. Dpt.
+Institute of Cell Physiology and Cellular Biosystems, and Light Microscopy Centre, University of Rostock, Universitatsplatz 2, D-18051 Rostock, Germany

Co-operative processes have been suggested to be the physical grounds that profoundly influence space-temporal organization of cellular function. The degree of its general occurrence and the characteristics of such cooperativity are however poorly understood. Despite improvements in the resolution and sensitivity of commonly used DIC and fluorescence microscopy direct measurements of enzyme dynamics are not possible. Since ATPase function implicates conformational changes it is to be expected that these are accompanied by the changes of refractive index. Changes of refractive index when resulting from a sufficiently large number of molecules lead to detectable and space-temporally correlated changes of local Optical Path Difference (OPD). The OPD changes are measured with a novel method, Dynamic Phase Microscopy (DPM), providing spatial resolution up to 100 nm and temporal resolution of tens of milliseconds. Using this technique the co-operative activity of F1F0 ATPase complexes incorporated into liposomes was studied. The OPD fluctuations were measured with DPM when liposome aggregate were exposed to 1 mM ATP. The conformational transitions in ensembles of interacting ATPase molecules resulted in a specific type of synchronization of their movement and yielded locally restricted changes of refractive index and OPD. These and numerous measurements on blood cells, fibroblasts, neurons and other cellular and subcellular specimens showing similar co-operative effects led us to propose that the coherent states and co-operative processes are a common feature of living cells that can be adequately studied by DPM.
 

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