Sjuvarsson, Elena
- Institutionen för husdjurens biovetenskaper, Sveriges lantbruksuniversitet
Forskningsartikel2015Vetenskapligt granskad
Sjuvarsson, Elena; Marquez, Victor E; Eriksson, Staffan
Here bicyclo[3.1.0]hexane locked deoxycytidine (S-MCdC, N-MCdC), and deoxyadenosine analogs (S-MCdA and N-MCdA) were examined as substrates for purified preparations of human deoxynucleoside kinases: dCK, dGK, TK2, TK1, the ribonucleoside kinase UCK2, two NMP kinases (CMPK1, TMPK) and a NDP kinase.dCK can be important for the first step of phosphorylation of S-MCdC in cells, but S-MCdCMP was not a substrate for CMPK1, TMPK, or NDPK.dCK and dGK had a preference for the S-MCdA whereas N-MCdA was not a substrate for dCK, TK1, UCK2, TK2, dGK nucleoside kinases. The cell growth experiments suggested that N-MCdC and S-MCdA could be activated in cells by cellular kinases so that a triphosphate metabolite was formed.List of abbreviations: ddC, 2 ', 3 '-didioxycytosine, Zalcitabine; 3TC, beta-L-(-)-2 ',3 '-dideoxy-3 '-thiacytidine, Lamivudine; CdA, 2-cloro-2 '-deoxyadenosine, Cladribine; AraA, 9-beta-D-arabinofuranosyladenine; hCNT 1-3, human Concentrative Nucleoside Transporter type 1, 2 and 3; hENT 1-4, human Equilibrative Nucleoside Transporter type 1, 2, 3, and 4.
nucleoside and nucleotide kinases; mechanism of action studies; Modified nucleosides
Nucleosides, Nucleotides and Nucleic Acids
2015, Volym: 34, nummer: 8, sidor: 544-564 Utgivare: TAYLOR & FRANCIS INC
Cell- och molekylärbiologi
DOI: https://doi.org/10.1080/15257770.2015.1031248
https://res.slu.se/id/publ/75557