## 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
The thermal induced helix—β transition of poly(Nε-methyl-L-lysine) and poly(Nδ-ethyl-L-ornithine) in aqueous solution
✍ Scribed by Hiroyuki Yamamoto; Jen Tsi Yang
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1974
- Tongue
- English
- Weight
- 380 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Uncharged poly(N^ε^‐methyl‐L‐lysine) (PMLL) and its isomer, poly(N^δ^‐ethyl‐L‐ornithine) (PELO), in alkaline solution (pH ca. 12) undergo a helix‐to‐β transition upon mild heating at 50°C or higher in a manner similar to that of poly(L‐lysine) (PLL). The rate of conversion follows the order: PMLL < PELO < PLL. The helix can be regenerated upon cooling near zero degrees, for instance, after more than 12 hr at 2°C. At concentrations less than 0.02% the β form is intramolecular, but at higher concentrations both intra‐ and intermolecular β forms are generated. Poly(N^δ^‐methyl‐L‐ornithine) (PMLO), an isomer of PLL, behaves like poly(L‐ornithine); uncharged PMLO in alkaline solution is partially helical and becomes disordered at elevated temperatures.
📜 SIMILAR VOLUMES
## Abstract The conformational phase diagram of poly(L‐lysine) (4.6 × 10^−4^ __M__, residue) in sodium dodecyl sulfate (1.6 × 10^−2^ __M__) solution was constructed from circular dichroism results at various temperatures and pH's. Poly(L‐lysine)–sodium dodecyl sulfate complexes undergo a β–helix tr