In this brief note we extend our previous low-temperature specific heat measurements' on the simplest homopolypeptide polyglycine (Gly),, to the high-temperature range of 15@375 K using differential scanning calorimetry. Polyglycine, or poly(C0-CHR-NH) with R = H. is dimorphic in the solid state,' e
Fluctuations and mechanical strength of α-helices of polyglycine and poly(L-alanine)
✍ Scribed by Yukio Suezaki; Nobuhiro Gō
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1976
- Tongue
- English
- Weight
- 922 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
By using the static correlations of fluctuations in the dihedral angles of the α‐helices of polyglycine and poly(L‐alanine) calculated previously, geometrical fluctuations of a section (consisting of up to 18 peptide units) of the α‐helices of infinite length are calculated. These fluctuations are found to differ in some respects (e.g., the dependence of amplitudes on the length of section) from those of a circular rod made of homogeneous continuous material. However, the moduli of the mechanical strengths (tensile Young's modulus, bending Young's modulus, and the shear modulus) of a circular rod are calculated, whose geometrical fluctuations are approximately equal to the fluctuations of a section consisting of 18 peptide units. They are of the order of 10^11^ dyn/cm^2^. The tensile rigidity, flexural rigidity, and torsional rigidity are calculated to be 1.20 × 10^−3^ dyn, 2.46 × 10^−19^ dyn·cm^2^ and 1.79 × 10^−19^ dyn·cm^2^ for polyglycine, and 1.96 × 10^−3^ dyn, 4.05 × 10^−19^ dyn·cm^2^ and 3.28 × 10^−19^ dyn·cm^2^ for poly(L‐alanine), respectively.
📜 SIMILAR VOLUMES
Heat capacities of polyglycine, poly( L-alanine), and poly (L-valine) were analyzed using approximate group vibrations and fitting of the skeletal vibrations to a two-parameter ( 01, O3 ) Tarasov function. New experimental data were measured by differential scanning calorimetry in the temperature ra
Polarized Raman spectra were obtained on well oriented Ðlms of a-helical poly(L-alanine) (a-PLA) and its Ndeuterated analogue in order to obtain deÐnitive assignments of the modes. Such assignments were aided E 2 -species by an analysis of factors that can lead to "cross-talkÏ between A, and spectra
Polarized ir spectra of oriented films of ␣-helical poly(L-alanine) (␣-PLA) have been obtained as a function of residual solvent dichloroacetic acid (DCA). The amide A, B, II, and V regions exhibit multiple bands whose structure depends on the residual DCA content, and those associated with the ␣ I
## Abstract The sequential copolymers of glycine and L‐alanine, L‐valine and L‐alanine, L‐leucine and L‐alanine, and L‐phenylalanine and L‐alanine and those containing the L‐proline residues were synthesized. The infrared spectra in the region from 700 to 200 cm^‐1^ were measured for these polypept