AbstractIn situ atomic force microscopy studies reveal a marked influence of the initial presence of hydrolysis products on the hydrolysis of supported phospholipid bilayers by phospholipase A2. By analysis of the nano-scale topography of a number of supported bilayers with different initial product concentrations, made by Langmuir-Blodgett deposition, we show that small depressions enriched in products are efficiently promoting enzyme degradation of the bilayer. These small depressions, which are indicative of phase separation, are initially present in samples with 75% products. The kinetics of phospholipase A2 exhibit under certain conditions an initial phase of slow hydrolysis, termed the latency phase, followed by a marked increase in t...
We monitored the action of phospholipase A(2) (PLA(2)) on L- and D-dipalmitoyl-phosphatidylcholine (...
AbstractAn important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme...
AbstractPhospholipase A2, a ubiquitous lipolytic enzyme that actively catalyses hydrolysis of phosph...
AbstractIn situ atomic force microscopy studies reveal a marked influence of the initial presence of...
AbstractAtomic force microscopy (AFM) is employed to reveal the morphological changes of the support...
AbstractWe have investigated the time course of the degradation of a supported dipalmitoylphosphatid...
The lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayers is for...
AbstractThe lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayer...
AbstractThe sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by monit...
ABSTRACT The sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by moni...
AbstractIn this paper we used AFM as an analytical tool to visualize the degradation of a phospholip...
AbstractSecretory phospholipase A2 (sPLA2) catalyzes the hydrolysis of glycerophospholipids. This en...
AbstractWe monitored the action of phospholipase A2 (PLA2) on L- and D-dipalmitoyl-phosphatidylcholi...
AbstractPhospholipase D from Streptomyces chromofuscus (PLDSc) is a soluble enzyme known to be activ...
We have monitored the composition of supported phospholipid bilayers during phospholipase A(2) hydro...
We monitored the action of phospholipase A(2) (PLA(2)) on L- and D-dipalmitoyl-phosphatidylcholine (...
AbstractAn important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme...
AbstractPhospholipase A2, a ubiquitous lipolytic enzyme that actively catalyses hydrolysis of phosph...
AbstractIn situ atomic force microscopy studies reveal a marked influence of the initial presence of...
AbstractAtomic force microscopy (AFM) is employed to reveal the morphological changes of the support...
AbstractWe have investigated the time course of the degradation of a supported dipalmitoylphosphatid...
The lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayers is for...
AbstractThe lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayer...
AbstractThe sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by monit...
ABSTRACT The sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by moni...
AbstractIn this paper we used AFM as an analytical tool to visualize the degradation of a phospholip...
AbstractSecretory phospholipase A2 (sPLA2) catalyzes the hydrolysis of glycerophospholipids. This en...
AbstractWe monitored the action of phospholipase A2 (PLA2) on L- and D-dipalmitoyl-phosphatidylcholi...
AbstractPhospholipase D from Streptomyces chromofuscus (PLDSc) is a soluble enzyme known to be activ...
We have monitored the composition of supported phospholipid bilayers during phospholipase A(2) hydro...
We monitored the action of phospholipase A(2) (PLA(2)) on L- and D-dipalmitoyl-phosphatidylcholine (...
AbstractAn important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme...
AbstractPhospholipase A2, a ubiquitous lipolytic enzyme that actively catalyses hydrolysis of phosph...