Ilík Petr, Krchnák Pavel, Tomek Pavel, Naus Jan
Department of Experimental Physics, Laboratory of Biophysics, Palacký University, Tr. Svobody 26, 77146, Olomouc, Czech Republic.
J Biochem Biophys Methods. 2002 May 31;51(3):273-81. doi: 10.1016/s0165-022x(02)00029-5.
In this work, we present a home-made two-dimensional (2-D) CCD imaging system for the monochromatic densitometry of plane gels and its application to the imaging and densitometry of chlorophyll (Chl)-containing proteins separated by non-denaturing polyacrylamide gel electrophoresis. The monochromatic imaging of separated green bands at the wavelengths corresponding to their absorption band increases their contrast. This allows a better visualization of the faint-green bands in the gel and using of samples with lower Chl content for the electrophoresis. By the comparison of 2-D densitograms of the same gel illuminated with 670 and 650 nm lights, that is, at the red absorption maximum of Chl a and b, respectively, we achieved a selective imaging of the complexes with different Chl a/b ratio. This approach was used to specify an unknown band that appeared in the gel of the sample prepared from the thylakoid membranes of preheated barley leaves.