NMR methods for studying membrane-active antimicrobial peptides

被引:131
作者
Strandberg, E
Ulrich, AS [1 ]
机构
[1] Forschungszentrum Karlsruhe, IFIA, D-76012 Karlsruhe, Germany
[2] Univ Karlsruhe, Inst Organ Chem, D-76131 Karlsruhe, Germany
关键词
amphiphilic antimicrobial peptides; solid state NMR; biomembranes; lipid bilayers; lipid-peptide interactions; peptide structure determination; isotope labeling; H-1-; (2) H-; C-13_; (15) N-; F-19-; and P-31-NMR;
D O I
10.1002/cmr.a.20024
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
NMR is a versatile tool for studying interactions between antimicrobial peptides and lipid membranes. Different approaches using both liquid state and solid state NMR are outlined here, with an emphasis on solid state NMR methods, to study the structures of antimicrobial peptides in lipid bilayers as well as the effect of these peptides on model membranes. Different NMR techniques for observing both peptides and lipids are explained, including H-2, C-13, N-15, and F-19 labels, or natural abundance H-1, C-13, or P-31. Previous studies in the field are extensively reviewed in easily accessible tables. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:89 / 120
页数:32
相关论文
共 248 条
[51]   INTERACTION OF MELITTIN WITH MIXED PHOSPHOLIPID-MEMBRANES COMPOSED OF DIMYRISTOYLPHOSPHATIDYLCHOLINE AND DIMYRISTOYLPHOSPHATIDYLSERINE STUDIED BY DEUTERIUM NMR [J].
DEMPSEY, C ;
BITBOL, M ;
WATTS, A .
BIOCHEMISTRY, 1989, 28 (16) :6590-6596
[52]   Hydrogen bond stabilities in membrane-reconstituted alamethicin from amide-resolved hydrogen-exchange measurements [J].
Dempsey, CE ;
Handcock, LJ .
BIOPHYSICAL JOURNAL, 1996, 70 (04) :1777-1788
[53]   A DEUTERIUM AND P-31 NUCLEAR-MAGNETIC-RESONANCE STUDY OF THE INTERACTION OF MELITTIN WITH DIMYRISTOYLPHOSPHATIDYLCHOLINE BILAYERS AND THE EFFECTS OF CONTAMINATING PHOSPHOLIPASE-A2 [J].
DEMPSEY, CE ;
WATTS, A .
BIOCHEMISTRY, 1987, 26 (18) :5803-5811
[54]   REVERSIBLE DISK-MICELLIZATION OF DIMYRISTOYLPHOSPHATIDYLCHOLINE BILAYERS INDUCED BY MELITTIN AND [ALA-14]MELITTIN [J].
DEMPSEY, CE ;
STERNBERG, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1061 (02) :175-184
[55]   HELICAL STRUCTURE AND ORIENTATION OF MELITTIN IN DISPERSED PHOSPHOLIPID-MEMBRANES FROM AMIDE EXCHANGE ANALYSIS INSITU [J].
DEMPSEY, CE ;
BUTLER, GS .
BIOCHEMISTRY, 1992, 31 (48) :11973-11977
[56]   THE INTERACTION OF AMINO-DEUTEROMETHYLATED MELITTIN WITH PHOSPHOLIPID-MEMBRANES STUDIED BY DEUTERIUM NMR [J].
DEMPSEY, CE ;
CRYER, GD ;
WATTS, A .
FEBS LETTERS, 1987, 218 (01) :173-177
[57]   AMIDE-RESOLVED HYDROGEN-DEUTERIUM EXCHANGE MEASUREMENTS FROM MEMBRANE-RECONSTITUTED POLYPEPTIDES USING EXCHANGE TRAPPING AND SEMISELECTIVE 2-DIMENSIONAL NMR [J].
DEMPSEY, CE .
JOURNAL OF BIOMOLECULAR NMR, 1994, 4 (06) :879-884
[58]   SPECIFICITY OF LIPID-PROTEIN INTERACTIONS AS DETERMINED BY SPECTROSCOPIC TECHNIQUES [J].
DEVAUX, PF ;
SEIGNEURET, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 822 (01) :63-125
[59]   nNOS inhibition, antimicrobial and anticancer activity of the amphibian skin peptide, citropin 1.1 and synthetic modifications - The solution structure of a modified citropin 1.1 [J].
Doyle, J ;
Brinkworth, CS ;
Wegener, KL ;
Carver, JA ;
Llewellyn, LE ;
Olver, IN ;
Bowie, JH ;
Wabnitz, PA ;
Tyler, MJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (06) :1141-1153
[60]   MECHANISTIC STUDIES OF LANTIBIOTIC-INDUCED PERMEABILIZATION OF PHOSPHOLIPID-VESICLES [J].
DRIESSEN, AJM ;
VANDENHOOVEN, HW ;
KUIPER, W ;
VANDEKAMP, M ;
SAHL, HG ;
KONINGS, RNH ;
KONINGS, WN .
BIOCHEMISTRY, 1995, 34 (05) :1606-1614