Differential absorption measurements of Cr4+-doped forsterite under picosecond excitation

1997 ◽  
Author(s):  
Konstantin V. Yumashev ◽  
Nickolai V. Kuleshov ◽  
P. V. Prokoshin ◽  
Alexander M. Malyarevich ◽  
Victor P. Mikhailov
Keyword(s):  
Differential Absorption ◽  
Picosecond Excitation ◽  
Absorption Measurements

Fluorescence and differential light absorption recordings with calcium probes and potential-sensitive dyes in skinned cardiac cells

1982 ◽  
Vol 60 (4) ◽  
pp. 556-567 ◽  
Author(s):  
Alexandre Fabiato
Keyword(s):  
Cardiac Cells ◽  
Arsenazo Iii ◽  
Optical Methods ◽  
Cardiac Cell ◽  
Differential Absorption ◽  
Fluorescence Measurements ◽  
Merocyanine 540 ◽  
Inverted Microscope ◽  
Optimum Wavelength ◽  
Absorption Measurements

This report describes an optical system for microspectrophotometry in a single cardiac cell from which the sarcolemma has been removed by microdissection (skinned cardiac cell). This system is attached to the high power inverted microscope used for the microdissection and includes (a) a single variable wavelength microspectrophotometer used to define the spectrum of a given dye or Ca2+ probe; and (b) a dual wavelength, differential microspectrophotometer used to record differentially between the optimum wavelength and a wavelength separated by 25–30 nm. Results are presented using the following optical methods: (a) fluorescence measurements with chlorotetracycline to monitor the amount of Ca2+ bound to the inner face of the sarcoplasmic reticulum (SR) membrane; (b) differential absorption measurements with arsenazo III to measure changes of myoplasmic [Ca2+]free resulting from Ca2+ release from the SR; (c) fluorescence and (or) differential absorption measurements with the potential-sensitive dyes merocyanine 540, NK 2367, and di-S-C3(5) to monitor changes of charge distribution on the SR membrane during Ca2+ accumulation in the SR, as well as before and during Ca2+-induced release of Ca2+ from the SR. A small and rapid signal is observed which precedes the Ca2+-induced release of Ca2+ from the SR. It is detected as an increase of Ca2+ binding inside the SR with chlorotetracycline and as a "hyperpolarization" with potential-sensitive dyes, while no transient change of myoplasmic [Ca2+]free is detected with arsenazo III. This small and rapid signal preceding the Ca2+ release may be a first hint to an understanding of the mechanism whereby a small increase of [Ca2+]free outside the SR triggers Ca2+ release from the SR.

scholarly journals The preparation of iodinated vancomycin and its distribution in bacteria treated with the antibiotic

1970 ◽  
Vol 116 (1) ◽  
pp. 83-92 ◽  
Author(s):  
H. R. Perkins ◽  
M. Nieto
Keyword(s):  
Cell Walls ◽  
Membrane Fraction ◽  
Living Cells ◽  
Differential Absorption ◽  
Micrococcus Lysodeikticus ◽  
Labelled Compound ◽  
Isolated Cell ◽  
Specific Peptide ◽  
Absorption Measurements

Vancomycin was radioactively labelled by iodination with 125I. Iodinated vancomycin was only a little less potent as an antibiotic than vancomycin itself. It was shown, both by chromatography and differential absorption measurements, to combine with acyl-d-alanyl-d-alanine residues. Radioactive vancomycin was used to follow the fate of the antibiotic in bacteria that had been subjected to the least concentration required to inhibit growth. Most of the radioactivity was in the cell walls, although some was found in the membrane fraction. The latter proportion increased during longer incubations with the antibiotic. Pre-formed protoplasts adsorbed very little vancomycin. Mg2+ removed labelled vancomycin from the mucopeptide of Bacillus licheniformis, but had little effect on the antibiotic adsorbed on Micrococcus lysodeikticus, either in vivo or on previously isolated cell walls. Specific peptide was shown to compete with cell walls for vancomycin and it also extracted from cell-wall samples the labelled compound that had been adsorbed on M. lysodeikticus living cells.

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