Probing membrane surfaces and the location of membrane-embedded peptides by (13)C MAS NMR using lanthanide ions.

Journal article

A simple but efficient (13)C MAS NMR method is presented for the determination of the location of embedded molecules such as peptides relative to biological membrane surfaces by exploiting the interaction with paramagnetic lanthanide ions. Using various aqueous Dy(3+) concentrations a distance-dependent differential paramagnetic quenching of NMR lipid resonance intensities for specific carbon sites was observed, with residues at the bilayer surface quenched effectively and hydrophobic sites unaffected by Dy(3+). Tested on the membrane-embedded 50 residue long M13 coat protein, (13)C labeled at its Val-29 and Val-31 residues, no paramagnetic quenching was observed for the peptide resonances by Dy(3+), suggesting that Val-29 and Val-31 are not in close proximity to the bilayer interface, but buried deeply inside the hydrophobic region of the lipid bilayer.

Authors: Gröbner, G; Glaubitz, C; Watts, A

• Publication status: Published
• Journal: Journal of magnetic resonance (San Diego, Calif. : 1997)
• Volume: 141
• Issue: 2
• Pages: 335-339
• Publication date: 1999-12-01
• DOI: 10.1006/jmre.1999.1894
• EISSN: 1096-0856
• ISSN: 1090-7807
• Language: English
• Keywords: Indicators and Reagents; Nuclear Magnetic Resonance, Biomolecular; Membrane Proteins; Metals, Rare Earth; Dimyristoylphosphatidylcholine; Lipid Bilayers; Peptides; Molecular Conformation; Carbon Isotopes