Pregled bibliografske jedinice broj: 1155047
Theoretical and experimental characterization of ferrocene tripeptides
Theoretical and experimental characterization of ferrocene tripeptides // Solid-State Science & Research 2021 : Book of Abstracts / Biliškov, Nikola ; Brekalo, Ivana ; Martinez, Valentina (ur.).
Zagreb: Institut Ruđer Bošković, 2021. str. 98-98 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Theoretical and experimental characterization of
ferrocene tripeptides
Autori
Šutalo, Petar ; Nuskol, Marko ; Đaković, Marijana ; Čakić-Semenčić, Mojca ; Kodrin, Ivan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Solid-State Science & Research 2021 : Book of Abstracts
/ Biliškov, Nikola ; Brekalo, Ivana ; Martinez, Valentina - Zagreb : Institut Ruđer Bošković, 2021, 98-98
ISBN
978-953-7941-35-2
Skup
Solid-State Science & Research 2021 (SCIRES2021)
Mjesto i datum
Zagreb, Hrvatska, 10.06.2021. - 11.06.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
ferrocene chromophore, circular dichroism, Cotton effect, ferrocene-based tripeptides, molecular mechanics, DFT, QTAIM
Sažetak
Organic chromophores can be used as the sensing elements for determination of the helicity of small peptides.[1, 2] The screw sense of the helix is correlated with the sign of the Cotton effect in circular dichroism (CD) spectra. Our group’s studies have shown that even small monosubstituted peptidomimetics derived from ferrocenamine show a signal in the CD spectra near 470 nm related to the ferrocene chromophore region.[3] Two novel stereoisomeric ferrocene-based tripeptides, Boc- Pro-Pro-Ala-NHFc, were synthesized and characterized experimentally (IR, NMR, CD). Theoretical conformational analysis performed in implicitly modelled solvent, nicely corroborates with the experimental findings about the hydrogen bond patterns. Varying in the chirality of only one amino acid, two stereoisomers show a significantly different distribution of the conformers. In both stereoisomers dominates only P-helix, although the unique orientation of the ferrocene subunit pointing away from the peptide chain is obtained in stereoisomer with heterochiral Pro-Pro amino acid sequence. A strong correlation was also noticed between the sign of the Cotton effect and dihedral angle describing the deviation between the amide and cyclopentadienyl ring plane.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
--IP-2020-02-9162 - Ferocenski analozi biomolekula: strukturna karakterizacija i biološka evaluacija (FER-AN-BIOMOL) (Barišić, Lidija) ( CroRIS)
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Ivan Kodrin
(autor)
Mojca Čakić
(autor)
Petar Šutalo
(autor)
Marijana Đaković
(autor)
Marko Nuskol
(autor)