15N-NMR spectroscopy. IV. Comparison of poly(L-lysine) and isopoly(L-lysine)
✍ Scribed by William E. Hull; Hans R. Kricheldorf; Martin Fehrle
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1978
- Tongue
- English
- Weight
- 873 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The natural abundance ^15^N‐nmr spectroscopy has been used to characterize the isomeric polymers (L‐Lys)~n~ and iso (L‐Lys)~n~ in aqueous solution. Although the peptide nitrogens of the two polymers have nearly equivalent shifts at pH < 10, the amino nitrogens differ by 5–6 ppm at pH < 7 and provide an easy means of identification. Furthermore, the polymers are distinguishable by the pK~a~ of the amino group and the basicity of the peptide nitrogen. At pH 10.3 and 25°C, (Lys)~n~ exhibits line broadening and an upfield chemical shift of the peptide nitrogen, indicative of the coil → helix transition. The formation of 100% helix may produce a shift as large as 5 ppm, which probably makes ^15^N‐nmr spectroscopy more suitable for studies of this transition.
📜 SIMILAR VOLUMES
## Abstract The conformational changes of poly‐__N__^ε^‐glutaryl‐L‐lysine (PGL) and poly‐__N__^ε^‐succinyl‐L‐lysine (PSL) in various salt solutions were studied by use of ORD and potentiometric titration measurements. The addition of alkali metal salts to the fully ionized PGL or PSL solution cause
## SYNOPSIS '.'C-nmr measurements are reported for samples of poly (L-lysine) both static and spinning a t the magic angle in the @-sheet form as a function of water content. T h e addition of water decreases the side-chain line widths considerably. Measurements of the cross-polarization time cons
## Abstract Poly(__N__^ε^‐stearyl‐L‐lysine) and poly(__N__^ε^‐pelargonyl‐L‐lysine) were synthesized both by polymerization of __N__^ε^‐pelargonyl and __N__^ε^‐stearyl‐L‐lysine NCA and by acylation of poly(L‐lysine) with pelargonyl and stearyl chloride. This second route has proven to be very useful