Pregled bibliografske jedinice broj: 212665
A novel bis-phenanthridine triamine with pH controlled binding to nucleotides and nucleic acids
A novel bis-phenanthridine triamine with pH controlled binding to nucleotides and nucleic acids // Organic & biomolecular chemistry, 3 (2005), 4373 - 4382 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 212665 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A novel bis-phenanthridine triamine with pH controlled binding to nucleotides and nucleic acids
Autori
Malojčić, Goran ; Piantanida, Ivo ; Marinić, Mirna ; Žinić, Mladen ; Marjanović, Marko ; Kralj, Marijeta ; Pavelić, Krešimir ; Schneider, Hans-Jörg
Izvornik
Organic & biomolecular chemistry (1477-0520) 3
(2005);
4373 - 4382
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
DNA; RNA; intercalator; pH control
Sažetak
The new bis-phenanthridine triamine (3) is characterised by three pKa values: 3.65 ; 6.0 and >7.5. Significant difference in protonation state of 3 at pH = 5 (four positive charges) and at pH = 7 (less than two positive charges) accounts for strong dependence of 3/nucleotide binding constants on nucleotide charge under acidic conditions, whereas at neutral pH all 3/nucleotide complexes are of comparable stability. All experimental data point at intercalation as dominant binding mode of 3 to polynucleotides. However, there is no indication of bis-intercalation of the two phenanthridine subunits in binding to double stranded polynucleotides, the respective complexes being most likely mono-intercalative. Thermal stabilisation of calf thymus DNA (ct-DNA) and poly A-poly U duplexes upon addition of 3 is significantly higher at pH = 5 than at neutral conditions. This is not the case with poly dA-poly dT, indicating that specific secondary structure of the latter, most likely the shape of the minor groove, plays a key role in complex stability. At pH = 5 3 acts as a fluorimetric probe for poly G (emission quenching) as opposed to other ss-polynucleotides (emission increase), while at neutral conditions this specificity is lost. One order of magnitude higher cytotoxicity of 3 compared to its "monomer" 4 can be accounted for by cooperative action of two phenanthridinium units and charged triamine linker. The results presented here are of interest to the development of e.g. sequence-selective cytostatic drugs, and in particular for the possibility to control the drug activity properties over binding to DNA and/or RNA by variation of the pH of its surrounding.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb
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