AbstractBinding of uniformly 13C labelled ATP to Na,K-ATPase was studied by 13C cross-polarization magic-angle spinning (CP-MAS) NMR. In the presence of 30mM Na+ , and with sample- and time-averaging, NMR spectra obtained at 4°C exhibited several resonances for the bound nucleotide. Chemical shifts suggested that site-specific changes in the micro-environment or conformation of the nucleotide occurred in the high affinity binding site. These experiments permit further studies of nucleotide dynamics, structure and binding under physiologically relevant conditions
A fluorescence ratiometric method utilising the probe eosin Y is presented for estimating the ATP bi...
International audienceThe detailed mechanism of ATP hydrolysis in ATP-binding cassette (ABC) transpo...
AbstractThe conformation of adenine nucleotides bound to bovine mitochondrial F1-ATPase was investig...
This paper addresses the question of long-range interactions between the intramembranous cation bind...
AbstractWhile an increasing number of structural biology studies successfully demonstrate the power ...
The Na, K-ATPase hydrolyzes ATP to drive the coupled extrusion and uptake of Na+ and K+ ions across ...
NMR relaxation enhancement by paramagnetic metals provides powerful restraints on the three-dimensio...
We demonstrate the use of dynamic nuclear polarization (DNP) to elucidate ligand binding to a membra...
AbstractThe rotational motion of an ouabain spin label with sheep kidney Na,K-ATPase has been measur...
AbstractA conformational transition between E2 and E1 forms of Na, K-ATPase induced by different nuc...
Using solid-state NMR approaches, it is now possible to define the structure and dynamics of binding...
NMR methods have been adopted to observe directly the characteristics of substrate binding to the ga...
We demonstrate the use of dynamic nuclear polarization (DNP) to elucidate ligand binding to a membra...
To investigate Na+ binding to the ion-binding sites presented on the cytoplasmic side of the Na,KATP...
AbstractWater proton nuclear relaxation measurements are used to detect and characterize four distin...
A fluorescence ratiometric method utilising the probe eosin Y is presented for estimating the ATP bi...
International audienceThe detailed mechanism of ATP hydrolysis in ATP-binding cassette (ABC) transpo...
AbstractThe conformation of adenine nucleotides bound to bovine mitochondrial F1-ATPase was investig...
This paper addresses the question of long-range interactions between the intramembranous cation bind...
AbstractWhile an increasing number of structural biology studies successfully demonstrate the power ...
The Na, K-ATPase hydrolyzes ATP to drive the coupled extrusion and uptake of Na+ and K+ ions across ...
NMR relaxation enhancement by paramagnetic metals provides powerful restraints on the three-dimensio...
We demonstrate the use of dynamic nuclear polarization (DNP) to elucidate ligand binding to a membra...
AbstractThe rotational motion of an ouabain spin label with sheep kidney Na,K-ATPase has been measur...
AbstractA conformational transition between E2 and E1 forms of Na, K-ATPase induced by different nuc...
Using solid-state NMR approaches, it is now possible to define the structure and dynamics of binding...
NMR methods have been adopted to observe directly the characteristics of substrate binding to the ga...
We demonstrate the use of dynamic nuclear polarization (DNP) to elucidate ligand binding to a membra...
To investigate Na+ binding to the ion-binding sites presented on the cytoplasmic side of the Na,KATP...
AbstractWater proton nuclear relaxation measurements are used to detect and characterize four distin...
A fluorescence ratiometric method utilising the probe eosin Y is presented for estimating the ATP bi...
International audienceThe detailed mechanism of ATP hydrolysis in ATP-binding cassette (ABC) transpo...
AbstractThe conformation of adenine nucleotides bound to bovine mitochondrial F1-ATPase was investig...