Pregled bibliografske jedinice broj: 897590
Design of Small Molecular Probes for Proteins and DNA / RNA
Design of Small Molecular Probes for Proteins and DNA / RNA // Book of Abstracts of the 10th Joint Meeting on Medicinal Chemistry / Basarić, Nikola ; Namjesnik, Danijel ; Perković, Ivana ; Stepanić, Višnja (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2017. str. 41-41 (plenarno, nije recenziran, sažetak, znanstveni)
CROSBI ID: 897590 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Design of Small Molecular Probes for Proteins and DNA / RNA
Autori
Piantanida, Ivo
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts of the 10th Joint Meeting on Medicinal Chemistry
/ Basarić, Nikola ; Namjesnik, Danijel ; Perković, Ivana ; Stepanić, Višnja - Zagreb : Hrvatsko kemijsko društvo, 2017, 41-41
ISBN
978-953-55232-8-4
Skup
10th Joint Meeting on Medicinal Chemistry
Mjesto i datum
Srebreno, Hrvatska, 25.06.2017. - 28.06.2017
Vrsta sudjelovanja
Plenarno
Vrsta recenzije
Nije recenziran
Ključne riječi
DNA recognition ; protein recognition ; fluorescence ; CD ; aggregation
Sažetak
Small molecules targeting DNA, RNA and/or proteins have attracted significant scientific interest not only because of their biomedicinal applications, but also due to widespread use of spectrophotometric markers in the related scientific research. For instance, fluorescent techniques significantly developed during the last three decades and now represent about 70% of the detection enabling technologies used in molecular biology and medicine. However, design of small molecule (Mw<600) for recognition of ds-DNA/RNA sequence or particular protein is very challenging due limited number of modifications in such restricted molecule size. Quite often, small modifications lead to change of target preference, for instance from DNA-targeting to protein-targeting molecule One of our research lines is focused on the generally under-investigated approach: exploitation of intrinsic property of some dyes for aggregation, whereby monomeric and aggregated dye differ strongly not only in target recognition but also in spectroscopic properties1. Thus, one dye molecule could bind with similar affinity to several targets (DNA, RNA, protein) giving different spectroscopic responses for each target: to some polynucleotide sequence dye would bind as monomer, for other sequence as dimer, and protein binding site would induce different spectroscopic response (Scheme 1). The ongoing research endeavours to establish for the low molecular weight dyes the structure-activity guidelines for fine tuning of DNA - RNA - protein preferences combined with recognition by set of sensitive and bio-applicable spectrometric methods.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
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
Profili:
Ivo Piantanida
(autor)