## 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
Conformational change of poly-Nε-glutary-L-lysine and poly-Nε-succinyl-L-lysine in aqueous salt solutions
✍ Scribed by Norio Murai; Shintaro Sugai
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1974
- Tongue
- English
- Weight
- 464 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
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 caused helix formation. The helical content of the polymers increases in the following sequences: at salt concentration 0–2 M, CsCl < KCl < LiCl < NaCl; and at 2–3 M, LiCl < CsCl < KCl ∼ NaCl. The preferential binding of the solvent components with various alkali metal salts of PGL or PSL was measured in LiCl, NaCl, and KCl solutions by means of equilibrium dialysis and differential refractometry. It was found that with increasing salt concentration, the polymers were preferentially hydrated in NaCl and KCl soultions; however the salt was preferentially bound to the polymers in LiCl solution. Such preferential binding was suggested to be closely related to conformational change. The addition of CaCl~2~ to polymer solutions led to the stabilization of the helical structure of PGL or PSL.
📜 SIMILAR VOLUMES
## 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 follo
Poly-L-lysine exists as an a-helix at high pH and a random coil at neutral pH. When the a-helix is heated above 27ЊC, the macromolecule undergoes a conformational transition to a b-sheet. In this study, the stability of the secondary structure of poly-L-lysine in solutions subjected to shear flow, a