Biophysical investigations of membrane perturbations by polypeptides using solid-state NMR spectroscopy (Review)

Molecular Membrane Biology

Volumn 17, Issue 3, 2000, Pages 135-142

  Bechinger, B ^a  

^a MAX PLANCK INSTITUTE OF BIOCHEMISTRY   (Germany)

Author keywords

Amphipathic peptide antibiotics; Colicin; Membrane protein; Oriented bilayer; Vpu channel protein

Indexed keywords

NITROGEN; POLYPEPTIDE;

CELL ACTIVITY; CELL KILLING; HYDROPHOBICITY; INFLUENZA VIRUS A; MEMBRANE POTENTIAL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PH MEASUREMENT; PRIORITY JOURNAL; PROTON TRANSPORT; REVIEW; SOLID STATE;

HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 0033646558     PISSN: 09687688     EISSN: None     Source Type: Journal    
DOI: 10.1080/09687680050197365     Document Type: Review

References (59)

1. Preparation of oriented lipid bilayer on ultrathin polymers for solid-state nmr analyses of peptide-membrane interactions
2. Towards membrane protein design: pH dependent topology of histidine-containing polypeptides
3. Structure and functions of channel-forming polypeptides: Magainins, cecropins, melittin and alamethicin
4. Structure and dynamics of the M13 coat protein signal sequence in membranes
5. The structure, dynamics and orientation of antimicrobial peptides in membranes by solid-state NMR spectroscopy
6. Solid-state NMR investigations on the structure and topological equilibria of polypeptides associated with biological membranes
7. Flat-coil probe for NMR spectroscopy of oriented membrane samples
8. Peptide structural analysis by solid-state NMR spectroscopy
9. Membrane helix orientation from linear dichroism of infrared attenuated total reflection spectra
10. Structure and interactions of magainin antibiotic peptides in lipid bilayers: A solid-state NMR investigation
11. Structure and orientation of the antibiotic peptide magainin in membranes by solid-state NMR spectroscopy
12. Beta-barrel proteins from bacterial outer membranes: Structure, function and refolding
13. Structure-function of the channel-forming colicins
14. Solid-state nuclear magnetic resonance characterization of gramicidin channel structure
15. Lipid polymorphism and the functional roles of lipids in biological membranes
16. Peptide helicity and membrane surface charge modulate the balance of electrostatic and hydrophobic interactions with lipid bilayers and biological membranes
17. Nuclear magnetic resonance measurements on a macroscopically ordered smectic liquid crystalline phase
18. Identifying nonpolar transbilayer helices in amino acid sequences of membrane proteins
19. Diversity of antimicrobial peptides and their mechanism of action
20. Direct determination of a molecular torsional angle by solid-state NMR
21. Membrane protein structures: The known world expands
22. Signal sequences
23. Biosynthesis and degradation of peptides derived from Xenopus laevis prohormones
24. Magic angle oriented sample spinning (MAOSS) - A new approach toward biomembrane studies
25. Dipolar recoupling in MAS spectra of biological solids
26. Macroscopic orientation of natural and model membranes for structural studies
27. 31P solid-state NMR spectroscopy investigation
28. Refinement of the geometry of the retinal binding pocket in dark adapted bacteriorhodpsin by heteronuclear solid-state NMR distance measurements
29. A novel peptide designated PYL and its precursor as predicted from cloned mRNA of Xenopus laevis skin
30. Magainin oligomers reversibly dissipate the proton electrochemical gradient in cytochrome oxidase liposomes
31. Transmembrane insertion of the colicin la hydrophobic hairpin
32. Uber das Giftsekret der Gelbbauchunke Bombina variegata L
33. Transmembrane four-helix bundle of influenza A M2 protein channel: Structural implications from helix tilt and orientation
34. Fluorescence energy transfer distance measurements. The hydrophobic helical hairpin of colicin A in the membrane bound state
35. All in the family: The toxic activity of pore-forming colicins
36. 15N solid-state NMR investigation in uniaxially aligned phospholipid bilayers
37. Membrane thinning caused by magainin 2
38. Orientational and aggregational states of magainin 2 in phospholipid bilayers
39. Molecular basis for membrane selectivity of an antimicrobial peptide, magainin 2
40. Relationship of membrane curvature to the formation of pores by magainin 2
41. High-resolution NMR of biological solids
42. Grazing incidence X-ray scattering of highly aligned phospholipid membranes containing antimicrobial peptides magainin 2
43. Structure of the membrane-pore-forming fragment of colicin A
44. Insights into membrane insertion based on studies of colicins
45. Identification of an ion channel activity of the Vpu transmembrane domain and its involvement in the regulation of virus release from HIV-1-infected cells
46. Mechanism of the binding, insertion, and destabilization of phospholipid bilayer membranes by α-helical antimicrobial and cell non-selective lytic peptides
47. The cDNA sequence coding for prepro-PGS (prepro-magainins) and aspects of the processing of this prepro-polypeptide
48. A 'molten-globule' membrane-insertion intermediate of the pore-forming domain of colicin A
49. Molecular cloning, cDNA sequencing, and chemical synthesis of cecropin B from Hyalophora cecropia
50. The interactions of histidine-containing amphipathic helical peptide antibiotics with lipid bilayers: The effects of charges and pH
51. The topology of lysine-containing amphipathic peptides in bilayers by CD, solid-state NMR and molecular modelling
52. The signal peptide
53. Membrane proteins: From sequence to structure
54. All-D amino acid-containing channel-forming antibiotic peptides
55. Solution structure and orientation of the transmembrane anchor domain of the HIV-1 encoded virus protein U (Vpu) by high-resolution and solid-state NMR spectroscopy
56. Magainins, a class of antimicrobial peptides from Xenopus skin: Isolation, characterization of two active form?s, and partial cDNA sequence of a precursor