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Backbone dynamics of human parathyroid hormone (1–34): Flexibility of the central region under different environmental conditions
Author(s) -
Scian Michele,
Marin Massimiliano,
Bellanda Massimo,
Tou Liqiang,
Alexander Joseph M.,
Rosenblatt Michael,
Chorev Michael,
Peggion Evaristo,
Mammi Stefano
Publication year - 2005
Publication title -
peptide science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.20355
Subject(s) - chemistry , parathyroid hormone , micelle , molecular dynamics , molecule , biophysics , crystallography , stereochemistry , calcium , computational chemistry , organic chemistry , aqueous solution , biology
Abstract The presence of a stable tertiary structure in the bioactive N‐terminal portion of parathyroid hormone (PTH), a major hormone in the maintenance of extracellular calcium homeostasis, is still debated. In this work, 15 N relaxation parameters of the 33 backbone amides of human PTH(1–34) were determined in phosphate‐buffered saline solution (PBS) and in the presence of dodecylphosphocholine (DPC) micelles. The relaxation parameters were analyzed using both the model‐free formalism (G. Lipari and A. Szabo, Journal of the American Chemical Society , 1982, Vol. 104, pp. 4546–4549) and the reduced spectral density functions approach (J.‐F. Lefevre, K. T. Dayie, J. W. Peng, and G. Wagner, Biochemistry , 1996, Vol. 35, pp. 2674–2686). In PBS, the region around Gly12 possesses a high degree of flexibility and the C‐terminal helix is less flexible than the N‐terminal one. In the presence of DPC micelles, the mobility of the entire molecule is reduced, but the stability of the N‐terminal helix increases relative to the C‐terminal one. A point of relatively higher mobility at residue Gly12 is still present and a new site of local mobility at residues 16–17 is generated. These results justify the lack of experimental nuclear Overhauser effect (NOE) restraints with lack of tertiary structure and support the hypothesis that, in the absence of the receptor, the relative spatial orientation of the two N‐ and C‐terminal helices is undefined. The flexibility in the midregion of PTH(1–34), maintained in the presence of the membrane‐mimetic environment, may enable the correct relative disposition of the two helices, favoring a productive interaction with the receptor. © 2005 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 84: 147–160, 2006 This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com

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