| Literature DB >> 8902620 |
S Saito1, S Watabe, H Ozaki, H Kigoshi, K Yamada, N Fusetani, H Karaki.
Abstract
Aplyronine A is a macrolide isolated from Aplysia kurodai. By monitoring fluorescent intensity of pyrenyl-actin, it was found that aplyronine A inhibited both the velocity and the degree of actin polymerization. Aplyronine A also quickly depolymerized F-actin. The kinetics of depolymerization suggest that aplyronine A severs F-actin. The relationship between the concentration of total actin and F-actin at different concentrations of aplyronine A suggests that aplyronine A forms a 1:1 complex with G-actin. From these results, it is concluded that aplyronine A inhibits actin polymerization and depolymerizes F-actin by nibbling. Comparison of the chemical structure of aplyronine A and another actin-depolymerizing macrolide, mycalolide B, suggests that the side-chain but not the macrolide ring of aplyronine A may account for its actin binding and severing activity.Entities:
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Year: 1996 PMID: 8902620 DOI: 10.1093/oxfordjournals.jbchem.a021449
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387