## Abstract There have been many reports that the nuclear magnetic resonance (nmr) spectra of a large number of polypeptides exhibit peak doubling of the α‐carbon and the α‐carbon proton in the helix–coil transition region. One apparent exception to this generalization has been polypeptides with io
A carbon-13 magnetic resonance study of the helix–coil transition in polyuridylic acid
✍ Scribed by Girjesh Govil; Ian C. P. Smith
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1973
- Tongue
- English
- Weight
- 545 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
The temperature‐dependent conformations of poly(U) in 0.5__M__ CsC1 have been studied by carbon‐13 nuclear magnetic resonance. The transition from random coil to an ordered structure results in broadening of lines in the ^13^C spectra, due to intramolecular ^1^H–^13^C dipolar interactions and restricted motions in the ordered state. Changes in the chemical shifts suggest that the bases are interacting below the transition temperature. The random coil form shows conformation preferences for internal rotation about C4′–C5′, C5′–O5′, and C3′–O 3′ bonds. The statistical randomness of the coil arises mainly because of flexibility about O–P bonds. The results are analyzed in conjunction with theoretical calculations and light‐scattering data.
📜 SIMILAR VOLUMES
## Abstract Poly(L‐tyrosine) is a random coil in dimethyl sulfoxide. Upon addition of dichloroacetic acid, poly(L‐tyrosine) undergoes a conformational transition centered at about 10% dichloroacetic acid. The transition is nearly complete at 20% dichloroacetic acid. Further addition of dichloroacet
The helix-coil transition for poly(P-benzyl-L-aspartate) [poly(Asp[OBzl])] in solvent mixtures of trifluoroacetic acid/deuterated chloroform (F3AcOH/CDC13) was studied by means of proton and carbon-13 nmr. Conformational fixation of the side chain occurs before the coil-helix transition of the backb