## Abstract The coil to helix conformational transitions undergone by poly‐γ‐benzyl‐~L~‐glutamate in solutions of haloacetic acids and various cosolvents were studied by means of proton magnetic resonance. The results indicate a very small solvent dependence of the α‐CH Helix–coil chemical shift di
PMR chemical shifts of TFA in poly(γ-benzyl L-glutamate) solutions
✍ Scribed by Kang-Jen Liu; S. J. Lignowski
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1970
- Tongue
- English
- Weight
- 262 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
The present communication describes a new way of studying helix–random coil transformations of polypeptide, poly‐(γ‐benzyl L‐glutamate), in benzene–trifluoracetic acid (TFA) and chloroform–TFA systems. The difference between the PMR chemical shift of TFA with and without the polypeptide, measured as Δ, may be used to follow the conformational transition. This technique is particularly useful for concentrated solutions, where the PMR peaks of the polymer are so broad that no valuable information may be derived. As the TFA content increases in the system (at constant polymer concentration), Δ decreases normally whether the polymer is helical or random. However, Δ changes in a different way in the helix–random coil transition region, and actually increases with increasing TFA content. This peculiar behavior is explained in terms of the solvation of the helix and random coil structures.
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## Abstract The helix–random‐coil transition process for poly‐γ‐benzyl‐L‐glutamate (PBG) in solvent mixtures trifluoroacetic acid/deuterochloroform (TFA/CDCl~3~) at different temperatures has been studied by nmr. The chemical shift behavior of the α‐CH resonances of the peptide chain and of the TFA
## Abstract The aggregation of poly(γ‐benzyl L‐glutamate) has been studied by measuring the specific Kerr constants (__B__/__c__) over a tenfold range of concentration and the intrinsic viscosities of solutions of a low molecular weight sample of the polymer in four solvent mixtures, viz., benzene–
The molecular-weight dependence of the rms radius of gyration »R 2 g … 1/2 of poly(gbenzyl L-glutamate ) (PBLG) in helicogenic solvents shows negative and positive deviations from expectations for an intact and rigid a-helix in the higher and lower molecular-weight ranges, respectively. In order to
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The helix-coil transition of poly(ybenzy1 L-glutamate) was studied by comparing proton magnetic relaxation behavior with optical activity studies. The transition temperatnre as determined by magnetic relaxation was lower than that obtained by optical activity. The relationship of these experiments