AbstractActin polymerization has been studied in the absence of excess nucleotide. Using G-actin ATP monomers, it was shown that mechanical shearing stimulates ATP hydrolysis. The procedures used enabled the detection of differential effects of phalloidin and tetramethylrhodamine-phalloidin, on the Pi-release step of the actin ATPase. It is concluded that tetramethylrhodamine, in contrast to phalloidin, accelerates Pi-release from actin filaments
Actin performs its myriad cellular functions by the growth and disassembly of its filamentous form. ...
1. If, in solutions of stable G-actin, ATP is replaced by ITP, UTP, CTP, GTP, ADP, or IDP in concent...
1. If, in solutions of stable G-actin, ATP is replaced by ITP, UTP, CTP, GTP, ADP, or IDP in concent...
AbstractActin polymerization has been studied in the absence of excess nucleotide. Using G-actin ATP...
AbstractThe hydrolysis of ATP that accompanies the polymerization of actin occurs on the F-actin sub...
<div><p>(A–C) Remaining unhydrolyzed γ-<sup>32</sup>P-AzidoATP on Arp2 (closed circle) and Arp3 (ope...
AbstractATP and insulin stimulate increases in phosphatidylinositol (3,4,5)-trisphosphate levels in ...
The cyclic peptide phalloidin, one of the toxic components of Amanita phalloides prevented the drop ...
AbstractWe have addressed the question whether water is part of the G- to F-actin polymerization rea...
The cyclic peptide phalloidin, one of the toxic components of Amanita phalloides prevented the drop ...
tions made concerning the actin ATPase and its role in the biological activity of actinand actin fil...
Cellular ATP depletion in diverse cell types results in the net conversion of monomeric G-actin to p...
AbstractWe have investigated the binding of PI, PIP and PIP2 to talin and the effect of phosphoinosi...
Current theory and experiments describing actin polymerization suggest that site-specific cleavage o...
AbstractConformational changes in subdomain 2 of actin were investigated using fluorescence probes d...
Actin performs its myriad cellular functions by the growth and disassembly of its filamentous form. ...
1. If, in solutions of stable G-actin, ATP is replaced by ITP, UTP, CTP, GTP, ADP, or IDP in concent...
1. If, in solutions of stable G-actin, ATP is replaced by ITP, UTP, CTP, GTP, ADP, or IDP in concent...
AbstractActin polymerization has been studied in the absence of excess nucleotide. Using G-actin ATP...
AbstractThe hydrolysis of ATP that accompanies the polymerization of actin occurs on the F-actin sub...
<div><p>(A–C) Remaining unhydrolyzed γ-<sup>32</sup>P-AzidoATP on Arp2 (closed circle) and Arp3 (ope...
AbstractATP and insulin stimulate increases in phosphatidylinositol (3,4,5)-trisphosphate levels in ...
The cyclic peptide phalloidin, one of the toxic components of Amanita phalloides prevented the drop ...
AbstractWe have addressed the question whether water is part of the G- to F-actin polymerization rea...
The cyclic peptide phalloidin, one of the toxic components of Amanita phalloides prevented the drop ...
tions made concerning the actin ATPase and its role in the biological activity of actinand actin fil...
Cellular ATP depletion in diverse cell types results in the net conversion of monomeric G-actin to p...
AbstractWe have investigated the binding of PI, PIP and PIP2 to talin and the effect of phosphoinosi...
Current theory and experiments describing actin polymerization suggest that site-specific cleavage o...
AbstractConformational changes in subdomain 2 of actin were investigated using fluorescence probes d...
Actin performs its myriad cellular functions by the growth and disassembly of its filamentous form. ...
1. If, in solutions of stable G-actin, ATP is replaced by ITP, UTP, CTP, GTP, ADP, or IDP in concent...
1. If, in solutions of stable G-actin, ATP is replaced by ITP, UTP, CTP, GTP, ADP, or IDP in concent...