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Polypeptide models of elastin: CD and NMR studies on synthetic poly(X-Gly-Gly) (1991)

Tamburro, A. M. ; Guantieri, V. ; Scopa, A. ; [et al.]

New York, NY [u.a.] : Wiley-Blackwell

Chirality 3 (1991), S. 318-323

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ISSN: 0899-0042

Keywords: nuclear magnetic resonance ; circular dichroism ; β-turn conformation ; Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Poly(X-Gly-Gly), simple structural models for the hydrophobic, proline-devoid, regions of elastin, have been synthesized and studied by circular dichroism and NMR spectroscopies. The results gave evidence of type II β-turns as the only ordered structure present in the polymers. The stability of the turns has been shown to decrease on hydration and to increase in the series Leu 〈 Ala 〈 Val 〈 Ile.

Additional Material: 7 Ill.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/chir.530030417

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