TENSION-STABILIZED PORES IN GIANT VESICLES - DETERMINATION OF PORE-SIZE AND PORE LINE TENSION

被引:270
作者
ZHELEV, DV
NEEDHAM, D
机构
[1] DUKE UNIV, DEPT MECH ENGN & MAT SCI, DURHAM, NC 27708 USA
[2] DUKE UNIV, CTR BIOCHEM ENGN, DURHAM, NC 27708 USA
[3] BULGARIAN ACAD SCI, CENT LAB BIOPHYS, BU-1113 SOFIA, BULGARIA
关键词
LIPOSOME; ELECTROPORATION; PORE SIZE; LINE TENSION;
D O I
10.1016/0005-2736(93)90319-U
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
We present the first observations of giant, long-existing, stabilized pores in vesicle membranes. Using a new experimental technique for studying the electropermeabilization of lipid membranes, giant liposomes (from 25 to 56 mum in diameter) were subjected to single, square, electric pulses (duration 150 mus and electric field strength from 63 to 126 kV/m). The liposomes were held by a micropipet and small membrane tensions were created by controlling the pipet suction pressure. The liposomes were loaded with media having different refractive index from the outside solution, and, under these conditions, the formation of pores in the pressurized liposome could be visualized by the jet of inside solution that flowed out from the membrane pore. By adjusting the membrane tension, pores were kept open, and pore lifetimes could be varied from tenths of a second to several seconds. The pore size was determined from the volumetric flow in the pore region and the measured pressure differences across the bilayer. It was clear from the experiments that only one pore remained opened after the pulse. The estimated pore radii were on the order of one micrometer. The pores were in a quasi-stationary state and when they closed they did so spontaneously in a quick process (in milliseconds). The isotropic membrane tension was determined for the same measurements and from determinations of both pore size and dynamic membrane tension the pore line tension was found. The line tension of the pore region was determined for two lipid compositions, stearoyloleoylphosphatidylcholine and stearoyloleoylphosphatidylcholine with 50 mol% cholesterol, and the obtained values for single bilayers were (0.92 +/- 0.07) - 10(-11) N and (3.05 +/- 0.12) . 10(-11) N, respectively.
引用
收藏
页码:89 / 104
页数:16
相关论文
共 43 条
[1]  
ABIDOR IG, 1979, BIOELECTROCH BIOENER, V6, P37
[2]   ELECTROPORATION - A UNIFIED, QUANTITATIVE THEORY OF REVERSIBLE ELECTRICAL BREAKDOWN AND MECHANICAL RUPTURE IN ARTIFICIAL PLANAR BILAYER-MEMBRANES [J].
BARNETT, A ;
WEAVER, JC .
BIOELECTROCHEMISTRY AND BIOENERGETICS, 1991, 25 (02) :163-182
[3]   THE RESEALING PROCESS OF LIPID BILAYERS AFTER REVERSIBLE ELECTRICAL BREAKDOWN [J].
BENZ, R ;
ZIMMERMANN, U .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 640 (01) :169-178
[4]   PRESSURE DROP DUE TO MOTION OF NEUTRALLY BUOYANT PARTICLES IN DUCT FLOWS [J].
BRENNER, H .
JOURNAL OF FLUID MECHANICS, 1970, 43 :641-&
[5]   PRESSURE DROP DUE TO MOTION OF NEUTRALLY BUOYANT PARTICLES IN DUCT FLOWS .2. SPHERICAL DROPLETS AND BUBBLES [J].
BRENNER, H .
INDUSTRIAL & ENGINEERING CHEMISTRY FUNDAMENTALS, 1971, 10 (04) :537-&
[6]   CHANGES IN MEMBRANE-STRUCTURE INDUCED BY ELECTROPORATION AS REVEALED BY RAPID-FREEZING ELECTRON-MICROSCOPY [J].
CHANG, DC ;
REESE, TS .
BIOPHYSICAL JOURNAL, 1990, 58 (01) :1-12
[7]   THE ELECTRICAL BREAKDOWN OF CELL AND LIPID-MEMBRANES - THE SIMILARITY OF PHENOMENOLOGIES [J].
CHERNOMORDIK, LV ;
SUKHAREV, SI ;
POPOV, SV ;
PASTUSHENKO, VF ;
SOKIRKO, AV ;
ABIDOR, IG ;
CHIZMADZHEV, YA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 902 (03) :360-373
[8]   THE SHAPE OF LIPID MOLECULES AND MONOLAYER MEMBRANE-FUSION [J].
CHERNOMORDIK, LV ;
KOZLOV, MM ;
MELIKYAN, GB ;
ABIDOR, IG ;
MARKIN, VS ;
CHIZMADZHEV, YA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 812 (03) :643-655
[9]   BREAKDOWN OF LIPID BILAYER-MEMBRANES IN AN ELECTRIC-FIELD [J].
CHERNOMORDIK, LV ;
SUKHAREV, SI ;
ABIDOR, IG ;
CHIZMADZHEV, YA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 736 (02) :203-213
[10]   STABILITY OF MEMBRANE SYSTEMS MODELED AS MULTILAYERED VISCOELASTIC FILMS [J].
DIMITROV, DS ;
ZHFLEV, DV ;
JAIN, RK .
JOURNAL OF THEORETICAL BIOLOGY, 1985, 113 (02) :353-377