AbstractThe lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayers is for the first time demonstrated in an atomic force microscopy (AFM) study. Simultaneous AFM measurements of the degree of bilayer degradation and the physical-chemical state of the membrane reveals growing nanoscale indentations in the membrane during the lag phase. It is argued that these indentations are domains of hydrolysis products (lysoPC/PC) which eventually trigger the burst. The rate of the rapid hydrolysis following the burst is found to be proportional to the length of the edge between membrane adsorbed and desorbed to the mica base. The observed maximal rate of membrane degradation is approx. 0.2 mmol lipid/min/mol lipase in ...
AbstractThe lipid-loss process has been studied with in situ atomic force microscopy (AFM) at six di...
AbstractAn important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme...
Recent advances in biomolecular design require accurate measurements performed in native or near-nat...
AbstractThe lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayer...
The lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayers is for...
AbstractIn situ atomic force microscopy studies reveal a marked influence of the initial presence of...
AbstractWe have investigated the time course of the degradation of a supported dipalmitoylphosphatid...
AbstractIn this paper we used AFM as an analytical tool to visualize the degradation of a phospholip...
AbstractThe sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by monit...
AbstractAtomic force microscopy (AFM) is employed to reveal the morphological changes of the support...
AbstractPhospholipase D from Streptomyces chromofuscus (PLDSc) is a soluble enzyme known to be activ...
ABSTRACT The sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by moni...
AbstractWe have monitored the composition of supported phospholipid bilayers during phospholipase A2...
AbstractWe monitored the action of phospholipase A2 (PLA2) on L- and D-dipalmitoyl-phosphatidylcholi...
AbstractThe behavior of a fluid supported membrane during hydrolysis by phospholipase A2 is for the ...
AbstractThe lipid-loss process has been studied with in situ atomic force microscopy (AFM) at six di...
AbstractAn important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme...
Recent advances in biomolecular design require accurate measurements performed in native or near-nat...
AbstractThe lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayer...
The lag-burst phenomenon in the phospholipase A2 mediated hydrolysis of phospholipid bilayers is for...
AbstractIn situ atomic force microscopy studies reveal a marked influence of the initial presence of...
AbstractWe have investigated the time course of the degradation of a supported dipalmitoylphosphatid...
AbstractIn this paper we used AFM as an analytical tool to visualize the degradation of a phospholip...
AbstractThe sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by monit...
AbstractAtomic force microscopy (AFM) is employed to reveal the morphological changes of the support...
AbstractPhospholipase D from Streptomyces chromofuscus (PLDSc) is a soluble enzyme known to be activ...
ABSTRACT The sensitivity of phospholipase A2 (PLA2) for lipid membrane curvature is explored by moni...
AbstractWe have monitored the composition of supported phospholipid bilayers during phospholipase A2...
AbstractWe monitored the action of phospholipase A2 (PLA2) on L- and D-dipalmitoyl-phosphatidylcholi...
AbstractThe behavior of a fluid supported membrane during hydrolysis by phospholipase A2 is for the ...
AbstractThe lipid-loss process has been studied with in situ atomic force microscopy (AFM) at six di...
AbstractAn important application of liquid cell Atomic Force Microscopy (AFM) is the study of enzyme...
Recent advances in biomolecular design require accurate measurements performed in native or near-nat...