Pregled bibliografske jedinice broj: 993722
Ligands simultaneously targeting various DNA, RNA or proteins: advantages of non-selective affinity combined with selective response
Ligands simultaneously targeting various DNA, RNA or proteins: advantages of non-selective affinity combined with selective response // 9th Central European Conference "Chemistry towards Biology”: Book of Abstracts: / András Perczel, Dóra K. Menyhárd (ur.).
Budimpešta, 2018. str. 18-18 (plenarno, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 993722 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Ligands simultaneously targeting various DNA, RNA
or proteins: advantages of non-selective affinity
combined with selective response
Autori
Piantanida, Ivo
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
9th Central European Conference "Chemistry towards Biology”: Book of Abstracts:
/ András Perczel, Dóra K. Menyhárd - Budimpešta, 2018, 18-18
Skup
Chemistry Towards Biology: Biomolecules as potential drugs (CTB)
Mjesto i datum
Budimpešta, Mađarska, 25.09.2018. - 27.09.2018
Vrsta sudjelovanja
Plenarno
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
DNA / RNA / protein recognition ; fluorescent markers ; circular dichroism ; target-aggregating dyes
Sažetak
Ligands targeting DNA, RNA and/or proteins have many biochemical and biomedical applications, whereby one of the most widespread uses is spectrophotometric markers. For instance, fluorescent markers and techniques significantly developed within the last decades and now represent about 70% of the detection enabling technologies used in molecular biology and medicine. However, the design of low molecular weight ligand (Mw<600) for recognition of ds- DNA/RNA sequence or particular protein is very challenging due to a limited number of modifications in such restricted molecule size. Quite often, small modifications in ligand structure lead to a change of target preference, for instance from DNA-targeting to protein- targeting molecule. One of our research interests deals with the generally under-investigated approach: exploitation of intrinsic property of some ligands for aggregation, whereby monomeric and aggregated ligand differ strongly not only in target recognition but also in spectroscopic properties1. Thus, one ligand molecule could bind with similar affinity to several targets (DNA, RNA, protein) giving different spectroscopic responses for each target: to some polynucleotide sequence ligand would bind as monomer, to another sequence as dimer, and protein binding site would again result in spectroscopic response differing from DNA/RNA signal (Scheme 1). The ongoing research endeavors to establish for the low molecular weight ligands the structure-activity guidelines for the fine-tuning of DNA - RNA - protein preferences combined with a recognition by a complementary set of sensitive and bio- applicable spectrometric methods (fluorescence and CD/LD spectrophotometry).
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)