Proton-induced permeability and fusion of large unilamellar vesicles by covalently conjugated poly(2-ethylacrylic acid)

被引:28
作者
Chen, T
Choi, LS
Einstein, S
Klippenstein, MA
Scherrer, P
Cullis, PR
机构
[1] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
[2] Inex Pharmaceut Corp, Burnaby, BC V5J 5J8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
liposome; intracellular delivery; carrier system; membrane fusion; polyelectrolyte;
D O I
10.3109/08982109909018658
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
Proton sensitive large unilamellar vesicles (LUV) were constructed by immobilization of the pH sensitive synthetic polymer poly(2-ethylacrylic acid) onto the outer monolayer. Thiolated poly(2-ethylacrylic acid) (PEAA-SH) was covalently conjugated to the surface of LUVs composed of egg phosphatidylcholine (EPC) and cholesterol (Chol) through the thiol-reactive maleimide lipid MPB-DSPE (N-(4-(p-maleimidophenyl)butyryl)-1,2-distearoyl-sn-glycero-3-phosphoethanolamine). The resulting PEAA-LUVs were shown to be stable at neutral pH (pH 7.0 to 8.0). Under acidic conditions, however, protonation of PEAA resulted in interaction with both the membrane it was linked to and the membrane of target vesicles, causing membrane destabilization and release of vesicle contents. Moreover, conjugated PEAA is shown to mediate fusion with target membranes in a pH dependent manner. PEAA-mediated permeabilization and vesicle-vesicle fusion occurred only when the polymer was covalently linked to the LUV surface. Proton dependent fusion of PEAA-LUVs was also observed with erythrocyte ghosts. This pH-dependent release of vesicle contents and fusion of PEAA-LUVs occurred below pH 6.8, which is well within the pH range expected to be encountered inside the endosomes in the endocytic pathway, indicating the potential of PEAA-LUVs as a drug carrier system for intracellular drug delivery.
引用
收藏
页码:387 / 405
页数:19
相关论文
共 48 条
[1]  
BAILEY AL, 1997, BIOCHIM BIOPHYS ACTA, V1342, P232
[2]   PENETRATION OF A CARDIOTOXIN INTO CARDIOLIPIN MODEL MEMBRANES AND ITS IMPLICATIONS ON LIPID ORGANIZATION [J].
BATENBURG, AM ;
BOUGIS, PE ;
ROCHAT, H ;
VERKLEIJ, AJ ;
DEKRUIJFF, B .
BIOCHEMISTRY, 1985, 24 (25) :7101-7110
[3]  
BLUMENTHAL R, 1983, J BIOL CHEM, V258, P3409
[4]   PREPARATION, PROPERTIES, AND APPLICATIONS OF RECONSTITUTED INFLUENZA-VIRUS ENVELOPES (VIROSOMES) [J].
BRON, R ;
ORTIZ, A ;
DIJKSTRA, J ;
STEGMANN, T ;
WILSCHUT, J .
METHODS IN ENZYMOLOGY, 1993, 220 :313-331
[5]   RECENT ADVANCES IN LIPOSOMAL DRUG-DELIVERY SYSTEMS [J].
CHONN, A ;
CULLIS, PR .
CURRENT OPINION IN BIOTECHNOLOGY, 1995, 6 (06) :698-708
[6]   BIODISTRIBUTION OF PH-SENSITIVE IMMUNOLIPOSOMES [J].
CONNOR, J ;
NORLEY, N ;
HUANG, L .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 884 (03) :474-481
[7]   PH-SENSITIVE LIPOSOMES - ACID-INDUCED LIPOSOME FUSION [J].
CONNOR, J ;
YATVIN, MB ;
HUANG, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (06) :1715-1718
[8]   EFFECTS OF FUSOGENIC AGENT ON MEMBRANE STRUCTURE OF ERYTHROCYTE-GHOSTS AND MECHANISM OF MEMBRANE-FUSION [J].
CULLIS, PR ;
HOPE, MJ .
NATURE, 1978, 271 (5646) :672-674
[9]   A PHASE-I/II STUDY OF INTRAPERITONEALLY ADMINISTERED DOXORUBICIN ENTRAPPED IN CARDIOLIPIN LIPOSOMES IN PATIENTS WITH OVARIAN-CANCER [J].
DELGADO, G ;
POTKUL, RK ;
TREAT, JA ;
LEWANDOWSKI, GS ;
BARTER, JF ;
FORST, D ;
RAHMAN, A .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1989, 160 (04) :812-819
[10]   STUDIES ON THE MECHANISM OF MEMBRANE-FUSION - ROLE OF HEADGROUP COMPOSITION IN CALCIUM-INDUCED AND MAGNESIUM-INDUCED FUSION OF MIXED PHOSPHOLIPID-VESICLES [J].
DUZGUNES, N ;
WILSCHUT, J ;
FRALEY, R ;
PAPAHADJOPOULOS, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 642 (01) :182-195