Pregled bibliografske jedinice broj: 884230
Synthesis of dipeptides containing photochemically reactive modifiyed tyrosine and evaluation of their dna binding
Synthesis of dipeptides containing photochemically reactive modifiyed tyrosine and evaluation of their dna binding // 10th Joint Meeting on Medical Chemistry : Book of Abstracts / Basarić, Nikola ; Namjesnik, Danijel ; Perković, Ivana ; Stepanić, Višnja (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2017. str. 121-121 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Synthesis of dipeptides containing photochemically reactive modifiyed tyrosine and evaluation of their dna binding
Autori
Husak, Antonija ; Matić, Josipa ; Piantanida, Ivo ; Basarić, Nikola
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
10th Joint Meeting on Medical Chemistry : Book of Abstracts
/ Basarić, Nikola ; Namjesnik, Danijel ; Perković, Ivana ; Stepanić, Višnja - Zagreb : Hrvatsko kemijsko društvo, 2017, 121-121
ISBN
978-953-55232-8-4
Skup
10th Joint Meeting of Medicinal Chemistry
Mjesto i datum
Dubrovnik, Hrvatska, 25.06.2017. - 28.06.2017
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
quinone methides ; peptides ; DNA
Sažetak
Quinone methides (QMs) are recative intermediates with a potential in the development of new leads for drugs owing to their reactivity with DNA, proteins and enzymes [1]. In particular, some anticancer antibiotics such as mitomycine base their action on metabolic formation of QMs and subsequent DNA cross-linking. Therefore, it is important to investigate different classes of simple QMs as potential anticancer agents. However, QM are reactive intermediates with short inherent lifetimes, so they have to be prepared in situ in the living cells. An excellent methodology for the generation of QMs in the biological systems are photochemical reactions of deamination or dehydration [2]. We have recently demonstrated that tyrosine derivatives can be modified into QM precursors and imbedded in proteins where they remain photochemically reactive [3]. Furthermore, it is known that photo-triggered DNA alkylation by QMs can be significantly enhanced by binding QM precursors to the DNA intercallators [4]. Here we present synthesis of dipeptides 1 and 2 that contain two unnatural amino acids, photochemically reactive tyrosine derivative and aminoacid bearing DNA intercalators- phenantridine [5] or pyrene [6]. Their non-colvalent and photo-triggered covalent DNA binding ability will be investigated.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
IP-2014-09-6312 - Supramolekulska kontrola fotokemijskih reakcija eliminacije (SupraPhotoE) (Basarić, Nikola, HRZZ - 2014-09) ( CroRIS)
HRZZ-IP-2013-11-1477 - Višenamjensko očitavanje DNA/RNA sekundarne strukture molekularnim kemijskim senzorima (DNA/RNA-MolSense) (Piantanida, Ivo, HRZZ - 2013-11) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb