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Structure and conformation of Arg8 vasopressin modified analogs

✍ Scribed by Edyta Podstawka-Proniewicz; Dariusz Sobolewski; Adam Prahl; Younkyoo Kim; Leonard M. Proniewicz


Book ID
102429572
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
282 KB
Volume
43
Category
Article
ISSN
0377-0486

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✦ Synopsis


Abstract

Fourier‐transform Raman and infrared spectra were acquired for four arginine vasopressin (AVP) analogs containing L‐diphenylalanine (Dpa): [Dpa^2^]AVP, [Cpa^1^,Dpa^2^]AVP, [Dpa^3^]AVP, and [Cpa^1^,Dpa^3^]AVP (where Cpa denotes 1‐mercaptocyclohexaneacetic acid). We compared and analyzed these spectra. In addition, the Raman spectra were compared to the corresponding surface‐enhanced Raman scattering spectra recorded in an aqueous silver colloidal dispersion. Silver colloidal dispersions prepared by the simple borohydride reduction of silver nitrate were used as substrates. The geometry of these molecules etched on the silver surface was deduced from the observed changes in the intensity enhancement, breadth, and shift in wavenumber of the Raman bands in the spectra of the bound versus free species. Based on the obtained data, adsorption mechanisms were proposed for each case, and the suggested adsorbate structures were compared. All the molecules were thought to adsorb onto a silver surface via a phenyl ring, free electron pairs on the sulfur atom, and CO and CONH‐bonds. However, the orientation of these fragments on the colloidal silver surface and the strength of the interactions with this surface are different. For [Dpa^3^]AVP and [Cpa^1^,Dpa^3^]AVP, a strong interaction among the—CCN‐peptide fragment and the colloidal silver surface occurs. Copyright © 2011 John Wiley & Sons, Ltd.


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