## 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
Poly(ε-L-lysine): Synthesis and conformation
✍ Scribed by D. R. S. Kushwaha; K. B. Mathur; D. Balasubramanian
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1980
- Tongue
- English
- Weight
- 589 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
The synthesis of poly(ε‐L‐lysine) is described. This is a poly(ε‐amino acid) in which the ε‐amino group of lysine is condensed with the α‐carboxyl group to produce a chain backbone that is a variant of the usual one seen in proteins and the side chain is the α‐amino group. Conformational studies of poly(ε‐L‐lysine) and its t‐butyloxycarbonyl derivative suggest the likelihood of a chain order that is formally similar to the antiparallel pleated‐sheet conformation of proteins.
📜 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
The effect of the number of methylene groups in the side chains on the conformation of polypeptides is assessed for three poly(L-lysine) homologs with R = -(CHz),,NHz. Circular dichroism studies show a pH-induced helix-coil transition in 0.05 M KCl with midpoints a t 9.6, 9.0, and 8.7 for n = 5, 6,