## Abstract The binding process between sodium poly(L‐glutamate) and __trans__‐2,2′,2″,2‴‐tetrapyridyl‐Fe(III) complex ions in aqueous solution at pH around 7 has been studied by means of equilibrium dialysis and optical measurements. The binding isotherm indicates the occurrence of a cooperative p
Circular dichroism of the complex between N-N′-diethylpseudoisocyanine and sodium poly(L-glutamate) in aqueous solutions
✍ Scribed by M. K. Pal; M. Mandel
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1977
- Tongue
- English
- Weight
- 438 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
In the presence of sodium poly(L‐glutamate) at pH = 7.5 the dye pseudoisocyanine in dilute aqueous solution (C~d~ = 1.10 × 10^−5^ M) and low P/D values exhibits an absorption spectrum with a very sharp red‐shifted J‐band. Under the same conditions circular dichroism (CD) in the visible region is observed with an extremely sharp peak at the position of the J‐band. At pH = 4.6, where the polypeptide is in the α‐helix conformation, no such J‐band is observed and no CD spectrum can be detected at the same P/D values. CD spectra in the uv range demonstrate that the occurrence of the dye–polypeptide complex which gives rise to the J‐band at slightly alkaline pH is not accompanied by a conformational transition of the polypeptide towards the α‐helical form.
📜 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