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Conformational Studies in Solid State and Solution of Protected C-terminal Dipeptide Fragment (Boc-Phe-Pro-NH2) of Morphiceptin

Biserka Kojić-Prodić ; Ruđer Bošković Institute, P.O.B. 1016, HR-10001 Zagreb, Croatia
Snježana Antolić ; Ruđer Bošković Institute, P.O.B. 1016, HR-10001 Zagreb, Croatia
Marina Kveder ; Ruđer Bošković Institute, P.O.B. 1016, HR-10001 Zagreb, Croatia
Ivanka Zigrović ; Ruđer Bošković Institute, P.O.B. 1016, HR-10001 Zagreb, Croatia
Jurka Kidrič ; National Institute of Chemistry, P.O.B. 30, 61015 Ljubljana, Slovenia
Štefica Horvat ; Ruđer Bošković Institute, P.O.B. 1016, HR-10001 Zagreb, Croatia

Puni tekst: engleski, pdf (182 KB) str. 259-277 preuzimanja: 143* citiraj
APA 6th Edition
Kojić-Prodić, B., Antolić, S., Kveder, M., Zigrović, I., Kidrič, J. i Horvat, Š. (1999). Conformational Studies in Solid State and Solution of Protected C-terminal Dipeptide Fragment (Boc-Phe-Pro-NH2) of Morphiceptin. Croatica Chemica Acta, 72 (2-3), 259-277. Preuzeto s https://hrcak.srce.hr/132162
MLA 8th Edition
Kojić-Prodić, Biserka, et al. "Conformational Studies in Solid State and Solution of Protected C-terminal Dipeptide Fragment (Boc-Phe-Pro-NH2) of Morphiceptin." Croatica Chemica Acta, vol. 72, br. 2-3, 1999, str. 259-277. https://hrcak.srce.hr/132162. Citirano 14.11.2019.
Chicago 17th Edition
Kojić-Prodić, Biserka, Snježana Antolić, Marina Kveder, Ivanka Zigrović, Jurka Kidrič i Štefica Horvat. "Conformational Studies in Solid State and Solution of Protected C-terminal Dipeptide Fragment (Boc-Phe-Pro-NH2) of Morphiceptin." Croatica Chemica Acta 72, br. 2-3 (1999): 259-277. https://hrcak.srce.hr/132162
Harvard
Kojić-Prodić, B., et al. (1999). 'Conformational Studies in Solid State and Solution of Protected C-terminal Dipeptide Fragment (Boc-Phe-Pro-NH2) of Morphiceptin', Croatica Chemica Acta, 72(2-3), str. 259-277. Preuzeto s: https://hrcak.srce.hr/132162 (Datum pristupa: 14.11.2019.)
Vancouver
Kojić-Prodić B, Antolić S, Kveder M, Zigrović I, Kidrič J, Horvat Š. Conformational Studies in Solid State and Solution of Protected C-terminal Dipeptide Fragment (Boc-Phe-Pro-NH2) of Morphiceptin. Croatica Chemica Acta [Internet]. 1999 [pristupljeno 14.11.2019.];72(2-3):259-277. Dostupno na: https://hrcak.srce.hr/132162
IEEE
B. Kojić-Prodić, S. Antolić, M. Kveder, I. Zigrović, J. Kidrič i Š. Horvat, "Conformational Studies in Solid State and Solution of Protected C-terminal Dipeptide Fragment (Boc-Phe-Pro-NH2) of Morphiceptin", Croatica Chemica Acta, vol.72, br. 2-3, str. 259-277, 1999. [Online]. Dostupno na: https://hrcak.srce.hr/132162. [Citirano: 14.11.2019.]

Sažetak
The crystal structure of the protected C-terminal dipeptide fragment (Boc-Phe-Pro-NH2) of the μ-opioid receptor highly selective agonist, morphiceptin (Tyr-Pro-Phe-Pro-NH2), was determined; the crystals are monoclinic with space group P21 and unit cell dimensions: a = 11.5731(5), b = 6.4490(3), c = 15.4082(5) Å, β = 100.359(5)° and Z = 2. To examine the influence of proline on the conformation of peptide bond, the molecular conformation was studied in solid state and solution (using 1H and 13C NMR data). The X-ray analysis revealed the following conformations of peptide backbone: φ1 = -63.2(5)°, ψ1 = 156.1(4)°, ω1 =-174.3(4)°, φ2 =-66.0(5)° and ψ2 = 152.0(4)°. The conformation of the Boc group is trans-trans. Experimental data revealed the trans conformation about the Phe-Pro amide bond, both in solid state and solution (DMSO). The possibility of cis/trans isomerization about the peptide bond (ω1) was examined by theoretical calculations using BIOSYM software. Molecular modelling, including molecular dynamics simulations of the title dipeptide, is in favour of trans peptide bond.

Ključne riječi
C-terminal dipeptide; cis/trans isomerization; morphiceptin; conformational analysis; X-ray structure; NMR; molecular dynamics simulations

Hrčak ID: 132162

URI
https://hrcak.srce.hr/132162

Posjeta: 264 *