Journal
PHARMACEUTICALS
Volume 15, Issue 5, Pages -Publisher
MDPI
DOI: 10.3390/ph15050554
Keywords
nucleotidase; cN-IIIB; NT5C3B; nucleotide-based inhibitor; 7-methylguanosine
Categories
Funding
- National Science Centre in Poland [UMO-2017/24/C/NZ1/00169, UMO-2018/31/B/ST5/03821, UMO-2016/21/D/NZ1/02806, UMO-2019/32/T/ST4/00073]
- Foundation for Polish Science [TEAM/20162/13]
- Faculty of Physics, University ofWarsaw [(PP/BF) 501-D111-01-1110102]
- [POIG.02.01.00-14-122/09]
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This study aimed to develop molecular tools for advanced studies on the cellular role of cytosolic nucleotidase cN-IIIB. Through substrate and inhibitor property profiling of a library of 41 substrate analogs, several 7-benzylguanosine 5'-monophosphate derivatives were identified as potent, unhydrolyzable inhibitors of cN-IIIB. The inhibitory mechanism was elucidated using X-ray crystallography and molecular docking, and it was demonstrated that these compounds can inhibit m(7)GMP decay in cell lysates.
Cytosolic nucleotidases (cNs) catalyze dephosphorylation of nucleoside 5'-monophosphates and thereby contribute to the regulation of nucleotide levels in cells. cNs have also been shown to dephosphorylate several therapeutically relevant nucleotide analogues. cN-IIIB has shown in vitro a distinctive activity towards 7-mehtylguanosine monophosphate (m(7)GMP), which is one key metabolites of mRNA cap. Consequently, it has been proposed that cN-IIIB participates in mRNA cap turnover and prevents undesired accumulation and salvage of m(7)GMP. Here, we sought to develop molecular tools enabling more advanced studies on the cellular role of cN-IIIB. To that end, we performed substrate and inhibitor property profiling using a library of 41 substrate analogs. The most potent hit compounds (identified among m(7)GMP analogs) were used as a starting point for structure- activity relationship studies. As a result, we identified several 7-benzylguanosine 5'-monophosphate (Bn(7)GMP) derivatives as potent, unhydrolyzable cN-IIIB inhibitors. The mechanism of inhibition was elucidated using X-ray crystallography and molecular docking. Finally, we showed that compounds that potently inhibit recombinant cN-IIIB have the ability to inhibit m(7)GMP decay in cell lysates.
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