## Abstract pH titration measurements of polyβ __S__βcarboxymethylβLβcysteine were undertaken in the aqueous Nacl solution in relation to the Ξ² formβrandom coil transition. The titration curves show a marked molecular weight dependence because of the shortened chain length of materials. Comparison
Light-scattering and potentiometric-titration studies of poly-L-tyrosine in aqueous solution
β Scribed by Marilyn B. Senior; Sandra L. H. Gorrell; Eugene Hamori
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1971
- Tongue
- English
- Weight
- 928 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Synopsis
Aqiieoris solritions of poly-1,-tyrosine were studied by potentiometric titrations, lightsrat,teririg measrirements, and infrared spectroscopy in order to characterize the conformational changes the macromolecules exhibit when the hydrogen-ion concentration of the solutions is varied. It was found that when the pH of the system a t 25OC is lowered from a value of about 13 the poly-L-tyrosine molecules undergo a random-coil to 8-structrire coxformatioil change a t pTI ll..?. It appears, that iuider the experimental conditions used, the formatioil of the p structure is an iiit ramolecular process which involves the folding of the polymer backbone into several hairpins of antiparallel 6 structure. On frirther lowering of the plf of the solutions aggregatioii (pII ll.B3) arid subsequently precipitation (pH 11.2) takes place. Since the apparent pK of the polymer does not show a drastic change dririiig the r:tndom-coil to p-strlict,lire conformation change, it was concluded, that the thermodynamic driving force for this conformation change is mainly due to the electrostatic effect of the partidly charged side chains of the poly-L-tyrosine molecriles.
π SIMILAR VOLUMES
## Abstract The conformational transition of polyβLβtyrosine in 0.1__M__ KCl was investigated by ORD and infrared spectroscopy, potentiometric titration, and sedimentation velocity experiments. It is shown that the fully ordered conformer is obtained by slow titration of the random coil with 0.1__N
The objective has been to establish if those ions which are known to change the stability of the struct,ure of proteins, have any influence on the properties of ionizable polypeptides. Potentiometric titrations and complementary optical rotation data are presented for aqueous solutions of poly-L-lys
Diffusion coefficients of polyamidoamine cascade polymers (PAMAMs) were measured in aqueous solutions by dynamic light scattering and, after labeling with fluorescein isothiocyanate, by fluorescence photobleaching recovery. The dynamic light scattering results depended weakly on pH at a high salt co
The absorption and circular dichroism spectra of the 1:l copolymer (L-LYS, L-Tyr), have been investigated in aqueous solutions at pH ranging from 3 to 13. The spectral patterns indicate that the fully charged polyampholyte assumes a nonperiodic conformation on the acid and basic sides of the isoelec