Conformational analysis of human calcitonin in solution. |
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Authors: | Kiyoshi Ogawa Shigenori Nishimura Masamitsu Doi Hiroyuki Takashima Yoshinori Nishi Takuya Yoshida Tadayasu Ohkubo Yuji Kobayashi |
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Affiliation: | Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, 565-0871 Japan. |
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Abstract: | The solution conformation of human calcitonin in a mixture of 60% water and 40% trifluoroethanol has been determined by the combined use of 1H NMR spectroscopy and distance geometry calculations with a distributed computing technique. 1H NMR spectroscopy provided 195 distance constraints and 13 hydrogen bond constraints. The 20 best converged structures exhibit atomic rmsd of 0.43 A for the backbone atoms from the averaged coordinate position in the region of Asn3-Phe22. The conformation is characterized by a nearly amphiphilic alpha-helix domain that extends from Leu4 in the cyclic region to His20. There are no significant differences observed among the overall structures of a series of calcitonins obtained from ultimobranchial bodies, including those that possess 20- to 50-fold greater activity. Three aromatic amino acid residues, Tyr12, Phe16 and Phe19, form a hydrophobic surface of human calcitonin. Bulky side chains on the surface could interfere with the ligand-receptor interaction thereby causing its low activity, relative to those of other species. |
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Keywords: | calcitonin human calcitonin eel calcitonin NMR amphiphilic α‐helix |
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