Pregled bibliografske jedinice broj: 494086
Populations of the Three Major Backbone Conformations in 19 Amino-Acid Dipeptides
Populations of the Three Major Backbone Conformations in 19 Amino-Acid Dipeptides // Proceedings of the National Academy of Sciences of the United States of America, 108 (2011), 5; 1794-1798 doi:10.1073/pnas.1017317108 (međunarodna recenzija, članak, znanstveni)
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Naslov
Populations of the Three Major Backbone Conformations in 19 Amino-Acid Dipeptides
Autori
Grdadolnik, Jože ; Mohaček Grošev, Vlasta ; Baldwin, Robert S. ; Avbelj, Franc
Izvornik
Proceedings of the National Academy of Sciences of the United States of America (0027-8424) 108
(2011), 5;
1794-1798
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
backbone conformers ; amide III band ; spectral populations ; infrared and Raman spectra
Sažetak
The amide III region of the peptide infrared and Raman spectra has been used to determine the relative populations of the 3 major backbone conformations (PII, β and αR) in 19 amino-acid dipeptides. The results provide a benchmark for force field or other methods of predicting backbone conformations in flexible peptides. There are 3 resolvable backbone bands in the amide III region. The major population is either PII or β for all dipeptides except Gly while the αR population is measurable but always minor (≤ 10%) for 18 dipeptides. (The Gly φ, ψ map is complex and so is the interpretation of the amide III bands of Gly.) There are substantial differences in the relative β and PII populations among the 19 dipeptides. The band frequencies have been assigned as PII, 1317-1306 cm-1 ; αR, 1304-1294 cm-1 ; and β, 1294-1270 cm-1. The 3 bands were measured by both attenuated total reflection spectroscopy and by Raman spectroscopy. Consistent results, both for band frequency and relative population, were obtained by both spectroscopic methods. The β and PII bands were assigned from the dependence of the 3J(HN, Hα) coupling constant (known for all 19 dipeptides) on the relative β population. The PII band assignment agrees with one made earlier from Raman optical activity data. The temperature dependences of the relative β and PII populations fit the standard model with Boltzmann-weighted energies for alanine and leucine between 30 and 60 degrees C.
Izvorni jezik
Engleski
Znanstvena područja
Fizika, Kemija
POVEZANOST RADA
Projekti:
098-0982904-2898 - Fizika i primjena nanostruktura i volumne tvari (Ivanda, Mile, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Vlasta Mohaček Grošev
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
- EconLit
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- BIOSIS Previews (Biological Abstracts)
- CA Search (Chemical Abstracts)
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