Biophysical mechanisms of phospholipase A2 activation and their use in liposome-based drug delivery

被引:90
作者
Jorgensen, K
Davidsen, J
Mouritsen, OG
机构
[1] Univ So Denmark, Ctr Biomembrane Phys, MEMPHYS, Dept Phys, DK-5230 Odense M, Denmark
[2] Tech Univ Denmark, LiPlasome Pharma AS, Ctr Biomembrane Phys, MEMPHYS, DK-2800 Lyngby, Denmark
关键词
phospholipase A2; lipid domain; stealth liposome; pro-drug; pro-enhancer; anti-cancer drug;
D O I
10.1016/S0014-5793(02)03408-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Secretory phospholipase A(2) (PLA(2)) is a ubiquitous water-soluble enzyme found in venom, pancreatic, and cancerous fluid. It is also known to play a role in membrane remodeling processes as well as in cellular signaling cascades. PLA(2) is interfacially active and functions mainly on organized types of substrate, e.g. micelles and lipid bilayers. Hence the activity of the enzyme is modulated by the lateral organization and the physical properties of the substrate, in particular the structure in the nanometer range. The evidence for nano-scale structure and lipid domains in bilayers is briefly reviewed. Results obtained from a variety of experimental and theoretical studies of PLA(2) activity on lipid-bilayer substrates are then presented which provide insight into the biophysical mechanisms of PLA(2) activation on lipid bilayers and liposomes of different composition. The insight into these mechanisms has been used to propose a novel principle for liposomal drug targeting, release, and absorption triggered by secretory PLA(2). (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:23 / 27
页数:5
相关论文
共 46 条
[1]  
Abe T, 1997, INT J CANCER, V74, P245, DOI 10.1002/(SICI)1097-0215(19970620)74:3<245::AID-IJC2>3.0.CO
[2]  
2-Z
[3]  
Andresen TL, 2002, BIOPHYS J, V82, p148A
[4]   Two photon fluorescence microscopy of coexisting lipid domains in giant unilamellar vesicles of binary phospholipid mixtures [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :290-305
[5]  
BELL JD, 1991, METHOD ENZYMOL, V197, P249
[6]   Interfacial enzymology:: The secreted phospholipase A2-paradigm [J].
Berg, OG ;
Gelb, MH ;
Tsai, MD ;
Jain, MK .
CHEMICAL REVIEWS, 2001, 101 (09) :2613-2653
[7]   MOLECULAR MECHANISM OF THE LIPID VESICLE LONGEVITY INVIVO [J].
BLUME, G ;
CEVC, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1146 (02) :157-168
[8]   LIPID BILAYER HETEROGENEITIES AND MODULATION OF PHOSPHOLIPASE A(2) ACTIVITY [J].
BURACK, WR ;
BILTONEN, RL .
CHEMISTRY AND PHYSICS OF LIPIDS, 1994, 73 (1-2) :209-222
[9]   Changes in vesicle morphology induced by lateral phase separation modulate phospholipase A(2) activity [J].
Burack, WR ;
Dibble, ARG ;
Allietta, MM ;
Biltonen, RL .
BIOCHEMISTRY, 1997, 36 (34) :10551-10557
[10]   Synergistic permeability enhancing effect of lysophospholipids and fatty acids on lipid membranes [J].
Davidsen, J ;
Mouritsen, OG ;
Jorgensen, K .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2002, 1564 (01) :256-262