Table 1. Observed 2H Quadrupolar Splitting Magnitudes (kilohertz) for Labeled Alanines in Aligned Samples of GWALP23 and Arg-Containing Derivatives in DOPC Bilayersa.
| |Δνq| (kHz) for the
indicated labeled Ala residue in sequence |
|||||||||
|---|---|---|---|---|---|---|---|---|---|
| peptide | label typeb | pH | cholesterol contentc | A7 | A9 | A11 | A13 | A15 | A17 |
| GWALP23 | CD3 | – | 0 or 20% | 16.6 | 1.7 | 16.7 | 1.5 | 15.4 | 2.6 |
| GWALP23-R14 | CD3 | 2–13 | 0 or 20% | 26.5 | 5.5 | 16 | 13.1 | 1.3 | 28.1 |
| GWALP23-R12 | CD3 | 5.5 | 20% | 27 | 56 | – | – | 21.5 | 29.3 |
| GWALP23-R12 | CαD | 5.5 | 20% | 95 | 111 | – | – | – | – |
Oriented bilayer samples were prepared on glass plates with 10 mM buffer between pH 2 and 13 (see Methods). The data for GWALP23 (unbuffered) in DOPC are from ref (2).
Side-chain CD3 or backbone CαD label on the indicated Ala residue, A7–A17.
Amount of cholesterol (mole percent of total lipid) in the DOPC bilayer. The results for GWALP23 and GWALP23-R14 do not depend upon the cholesterol content. GWALP23-R12 occupies multiple states in the absence of cholesterol.13