## Abstract The rate of conformational change of aqueous poly(α‐L‐lysine) solutions was measured using the electric field pulse relaxation method with conductivity detection. The relaxation time as a function of pH exhibits two maxima. One is assigned to a proton transfer reaction and the other to
The application of surface tension measurements to the study of conformational transitions in aqueous solutions of poly-L-lysine
✍ Scribed by A. W. Neumann; M. A. Moscarello; R. M. Epand
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1973
- Tongue
- English
- Weight
- 583 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The change in surface tension of solutions of poly‐L‐lysine in water has been studied as a function of temperature at various pH values. The changes at various temperatures have been correlated with changes in the circular dichroic spectra reflecting conformational change. In addition to the major transition at 50°C attributed to the conversion of the α‐helical → β conformation, two other transitions have been observed at 30°C and 80°C.
A minimum in the surface tension value was observed at pH 10, near the pK value for poly‐L‐lysine. It was concluded that at this pH the concentration of hydrophobic groups at the surface was a maximum.
📜 SIMILAR VOLUMES
The absorption and circular dichroism spectra of the 1:l copolymer (L-LYS, L-Tyr), have been investigated in aqueous solutions at pH ranging from 3 to 13. The spectral patterns indicate that the fully charged polyampholyte assumes a nonperiodic conformation on the acid and basic sides of the isoelec
351 00 Padova, Ilaly synopsis Circular Dichroism measurements have been carried out on poly-L-lysine (PLL) and on random copolymers of lysine and phenylalanine a t various pH values and in the presence of different amounts of NaClOr. The results indicate that either the homopolymer or the copolymers
Water-insoluble films of poly-L-lysine, crosslinked with formaldehyde, were suspended in aqueous media and their relative lengths measured as a function of pH. A sharp transition of the polymer was observed in the pH range which corresponded with that observed in polylysine solutions by optical rota
## Abstract The Raman and infrared spectra of poly(L‐lysine) and poly(DL‐lysine) in solution are reported and the effects of various salts are investigated. The results demonstrate that α‐helix formation in solution is induced by specific salts and the spectral data support the hypothesis of region