## Abstract pH titration measurements of poly‐ __S__‐carboxymethyl‐L‐cysteine were undertaken in the aqueous Nacl solution in relation to the β form–random coil transition. The titration curves show a marked molecular weight dependence because of the shortened chain length of materials. Comparison
Potentiometric titration of poly-S-carboxyethyl-L-cysteine
✍ Scribed by Hiroshi Maeda; Shoichi Ikeda
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1971
- Tongue
- English
- Weight
- 603 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Potentiometric titration curves have been determined for aqueous solutions of poly-S-carboxyethyl-L-cysteine, which is subject, to the p-coil transition by a change in pH. Iteversibility and time dependence of the titration curves are examined by different methods in order to establish the condilions for obtaining equilibrium curves. The 0-coil transition is manifest at some region on the equilibrium titration curve, if pHlog (01/1 -0 1 ) is plotted against 01. Assuming a value, 4.00, for pKi,t, the free-energy change for the p-coil transition of uncharged polymer has been evaluated from the extrapolation of the observed titration curves and is found to depend on the ionic strength and polymer concentration. The Henderson-Hasselbach plot of the titration curve yields clearer distinction between the p-form and random coil, and it permits estimation of the content of @-form a t a given pH. Comparison of the conformational titration curve with the circular dichroic measurements leads to a value of -10,000'
for [e]223 for the pure p-structure. Precipitation which occurs a t low degrees of ionization and, especially, a t high ionic strength does not reveal any discontinuous change of the titration curve, which suggests t.hat the degree of ionization of the precipitated 8-form is not very different, from that in solut,ion.
📜 SIMILAR VOLUMES
Counterion activity of poly-8-carboxyethyl-L-cysteine in salefree solutions neutralized to various degrees with sodium hydroxide was determined either directly from the e.m.f measurements of concentration cells formed across a Na-glass electrode, or from the potentiometric titrations at different so
The interaction of CuC1, with poly(Scarboxymethy1-L-cysteine) (poly[Cys(CH,COOH)]) and poly(Scarboxyethy1-L-cysteine) (poly[Cys(CzH,COOH)]) were studied by absorption spectra and circular dichroism (CD). On mixing CuClz with polypeptide solutions, absorption bands appeared at 32C-325 nm in both poly
## Abstract The visible phase separation encountered in aqeuous system involving the β‐coil transition is investigated on poly‐__S__‐carboxyethyl‐L‐cysteine at a constant ionic strength of 0.2 molal. Solubility of the polymer decreases as the average charge density or pH is decreased, indicating th
The p-coil transition of poly(S-carboxymethyl-L-cysteine) (poly[Cys(CHzCOpH)]) and poly(S-carboxyethyl-L-cysteine) (poly[Cys((CHz)zCOzH)]) was followed by CD, potentiometric titration, and viscosity in the absence of added salt. These different properties give consistent results for poly[Cys((CHz)zC