Scinovex
article Open AccessTop 1% cited

Fluorimetry Study of <i>N</i>‐(1‐Pyrenyl)iodoacetamide‐Labelled F‐Actin

European Journal of Biochemistry · 1981 · Vol. 114(1) · pp. 33–38
Tsutomu KouyamaKoshin Mihashi

Abstract

A fluorescent reagent, N ‐(1‐pyrenyl)iodoacetamide, was conjugated to rabbit skeletal muscle actin at the site of the most reactive sulfhydryl group, and fluorescence characteristics (excitation and emission spectra, quantum yields, lifetimes) of the conjugate were investigated. Associated with polymerization of labelled G‐actin, the fluorescence intensity at 407 nm, after excitation at 365 nm, was enhanced by a factor of about 25. It was reduced to about 25% on the binding of heavy meromyosin (or subfragment 1). The results suggest that binding of heavy meromyosin to the protomer of F‐actin alters the local structure of the protomer towards a G‐actin‐like one.

Lanthanide and Transition Metal ComplexesPolymer Surface Interaction StudiesAdvanced MRI Techniques and ApplicationsIodoacetamideHeavy meromyosinChemistryFluorescencePolymerizationActinConjugatePhotochemistryBiophysicsBiochemistry
Citations
716
FWCI
13.53
field-weighted impact
References
12
Percentile
100%
vs. same field & year
Citations per year
Cited by
Inhibition of actin polymerization by latrunculin A
FEBS Letters · 1987 · 836 citations
References
The Regulation of Rabbit Skeletal Muscle Contraction
Journal of Biological Chemistry · 1971 · 4,524 citations
Related articles
Fluorimetry Study of <i>N</i>‐(1‐Pyrenyl)iodoacetamide‐Labelled F‐Actin
European Journal of Biochemistry · 1981 · 716 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.