Gramicidin A aggregation in supported gel state phosphatidylcholine bilayers

被引:103
作者
Mou, JX
Czajkowsky, DM
Shao, ZF
机构
[1] UNIV VIRGINIA,HLTH SCI CTR,DEPT MOL PHYSIOL & BIOL PHYS,CHARLOTTESVILLE,VA 22908
[2] UNIV VIRGINIA,HLTH SCI CTR,BIOPHYS PROGRAM,CHARLOTTESVILLE,VA 22908
关键词
D O I
10.1021/bi9520242
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
Using an atomic force microscope, supported bilayers of saturated phosphatidylcholine (in the gel state) containing various amounts of gramicidin A (gA) were imaged in aqueous solutions and at room temperature. gA clusters were directly observed for the first time under these conditions. It was found that, at a lower gA concentration, gA aggregated into domains, composed of small clusters along with a considerable amount of lipids. This basic aggregation unit. most likely a hexamer, remained the same for acyl chain lengths from 14 to 18 carbons. These small clusters were observed to form elongated aggregates (line type) but never into extended pure gA domains. When gA concentrations were increased, for bilayers with 16 carbons or less, gA aggregated into larger domains but the basic unit remained separated by lipid molecules. At about 5 mol % gA, a percolation-like transition occurred at which the line type aggregates were connected to each other. However, for bilayers with more than 16 carbons, multiple lamellar strucutres were formed at higher gA fractions and the top layer had a ripple-like surface morphology. The molecular mechanism for the formation of these peculiar structures remains to be elucidated.
引用
收藏
页码:3222 / 3226
页数:5
相关论文
共 39 条
[1]   MICROFABRICATION OF CANTILEVER STYLI FOR THE ATOMIC FORCE MICROSCOPE [J].
ALBRECHT, TR ;
AKAMINE, S ;
CARVER, TE ;
QUATE, CF .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1990, 8 (04) :3386-3396
[2]   H-1-NMR STUDY OF GRAMICIDIN-A TRANSMEMBRANE ION CHANNEL - HEAD-TO-HEAD RIGHT-HANDED, SINGLE-STRANDED HELICES [J].
ARSENIEV, AS ;
BARSUKOV, IL ;
BYSTROV, VF ;
LOMIZE, AL ;
OVCHINNIKOV, YA .
FEBS LETTERS, 1985, 186 (02) :168-174
[3]  
BUSATH DD, 1993, ANNU REV PHYSIOL, V55, P473
[4]   INTERACTIONS OF HELICAL POLYPEPTIDE SEGMENTS WHICH SPAN HYDROCARBON REGION OF LIPID BILAYERS - STUDIES OF GRAMICIDIN ALIPID-WATER SYSTEM [J].
CHAPMAN, D ;
CORNELL, BA ;
ELIASZ, AW ;
PERRY, A .
JOURNAL OF MOLECULAR BIOLOGY, 1977, 113 (03) :517-538
[5]   BIOMOLECULAR IMAGING WITH THE ATOMIC-FORCE MICROSCOPE [J].
HANSMA, HG ;
HOH, JH .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1994, 23 :115-139
[6]   X-RAY-SCATTERING WITH MOMENTUM-TRANSFER IN THE PLANE OF MEMBRANE - APPLICATION TO GRAMICIDIN ORGANIZATION [J].
HE, K ;
LUDTKE, SJ ;
WU, YL ;
HUANG, HW .
BIOPHYSICAL JOURNAL, 1993, 64 (01) :157-162
[7]  
Hille B., 1992, IONIC CHANNELS EXCIT
[8]   DEUTERIUM NMR OF 2HCO-VAL1...GRAMICIDIN-A AND 2HCO-VAL1-D-LEU2...GRAMICIDIN-A IN ORIENTED DMPC BILAYERS [J].
HING, AW ;
ADAMS, SP ;
SILBERT, DF ;
NORBERG, RE .
BIOCHEMISTRY, 1990, 29 (17) :4156-4166
[9]   TRYPTOPHANS IN MEMBRANE-PROTEINS - INDOLE RING ORIENTATIONS AND FUNCTIONAL IMPLICATIONS IN THE GRAMICIDIN CHANNEL [J].
HU, W ;
LEE, KC ;
CROSS, TA .
BIOCHEMISTRY, 1993, 32 (27) :7035-7047