Literature DB >> 7578091

Modulation of phospholipase A2: identification of an inactive membrane-bound state.

W R Burack1, M E Gadd, R L Biltonen.   

Abstract

Phospholipase A2-catalyzed hydrolysis of vesicular phospholipid has been used to model the modulation of an enzyme's function by membrane properties. Phospholipase A2's (PLA2) kinetics toward large unilamellar vesicles (LUV) composed of dipalmitoylphosphatidylcholine (DPPC) are anomalous; these is a slow initial phase of catalysis (a lag) which ends abruptly with a sudden increase in the catalytic rate (a burst). The sudden increase in activity due to the accumulation of a critical mole fraction of reaction products and substrate undergoes compositional phase separation. In this work, we address the molecular details of the coupling between compositional phase separation and activation of PLA2. A prominent model for this coupling is that compositional phase separation leads to a surface for which PLA2 has increased affinity, resulting in the recruitment of PLA2 from solution to the surface. Here, we show that the bulk of PLA2 is associated with the membrane at a time well before the abrupt increase in catalytic rate. This finding indicates that there must be a relatively inactive, membrane-bound state. Furthermore, PLA2's kinetics are anomalous even when the substrate comprises a surface to which PLA2 is bound throughout the time course. With DPPC LUV as the substrate, detailed time courses show that the description of the time course as a lag and a burst is inadequate. Instead, the time course consists of multiple phases of acceleration and deceleration. The data presented here suggest that all these various changes in catalytic rate may be due to product-induced changes in membrane properties. In particular, we suggest that nonequilibrium, microheterogeneities of lipid composition may underlie these very complicated kinetics.

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Year:  1995        PMID: 7578091     DOI: 10.1021/bi00045a024

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  7 in total

1.  In vitro behavior of marine lipid-based liposomes. Influence of pH, temperature, bile salts, and phospholipase A2.

Authors:  F Nacka; M Cansell; B Entressangles
Journal:  Lipids       Date:  2001-01       Impact factor: 1.880

2.  Influence of product phase separation on phospholipase A(2) hydrolysis of supported phospholipid bilayers studied by force microscopy.

Authors:  Lars K Nielsen; Konstatin Balashev; Thomas H Callisen; Thomas Bjørnholm
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

3.  Importance of membrane structural integrity for RPE65 retinoid isomerization activity.

Authors:  Marcin Golczak; Philip D Kiser; David T Lodowski; Akiko Maeda; Krzysztof Palczewski
Journal:  J Biol Chem       Date:  2010-01-25       Impact factor: 5.157

4.  Changes in a phospholipid bilayer induced by the hydrolysis of a phospholipase A2 enzyme: a molecular dynamics simulation study.

Authors:  M T Hyvönen; K Oörni; P T Kovanen; M Ala-Korpela
Journal:  Biophys J       Date:  2001-02       Impact factor: 4.033

5.  Toward understanding interfacial activation of secretory phospholipase A2 (PLA2): membrane surface properties and membrane-induced structural changes in the enzyme contribute synergistically to PLA2 activation.

Authors:  S A Tatulian
Journal:  Biophys J       Date:  2001-02       Impact factor: 4.033

6.  A two-photon view of an enzyme at work: Crotalus atrox venom PLA2 interaction with single-lipid and mixed-lipid giant unilamellar vesicles.

Authors:  Susana A Sanchez; Luis A Bagatolli; Enrico Gratton; Theodore L Hazlett
Journal:  Biophys J       Date:  2002-04       Impact factor: 4.033

7.  Amyloid-type fiber formation in control of enzyme action: interfacial activation of phospholipase A2.

Authors:  Christian Code; Yegor Domanov; Arimatti Jutila; Paavo K J Kinnunen
Journal:  Biophys J       Date:  2008-03-13       Impact factor: 4.033

  7 in total

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