-
Something wrong with this record ?
Thermodynamic Insights by Microscale Thermophoresis into Translesion DNA Synthesis Catalyzed by DNA Polymerases Across a Lesion of Antitumor Platinum-Acridine Complex
M. Hreusova, O. Novakova, V. Brabec
Language English Country Switzerland
Document type Journal Article
Grant support
18-09502S
Grantová Agentura České Republiky
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
33096927
DOI
10.3390/ijms21207806
Knihovny.cz E-resources
- MeSH
- DNA Adducts chemistry genetics metabolism MeSH
- Acridines chemistry pharmacology MeSH
- Biocatalysis MeSH
- DNA-Directed DNA Polymerase metabolism MeSH
- DNA biosynthesis MeSH
- Guanine metabolism MeSH
- Catalysis MeSH
- Nucleotides genetics metabolism MeSH
- DNA Repair MeSH
- DNA Replication MeSH
- Platinum Compounds chemistry pharmacology MeSH
- Thermal Diffusion MeSH
- Thermodynamics MeSH
- Publication type
- Journal Article MeSH
Translesion synthesis (TLS) through DNA adducts of antitumor platinum complexes has been an interesting aspect of DNA synthesis in cells treated with these metal-based drugs because of its correlation to drug sensitivity. We utilized model systems employing a DNA lesion derived from a site-specific monofunctional adduct formed by antitumor [PtCl(en)(L)](NO3)2 (complex AMD, en = ethane-1,2-diamine, L = N-[2-(acridin-9-ylamino)ethyl]-N-methylpropionamidine) at a unique G residue. The catalytic efficiency of TLS DNA polymerases, which differ in their processivity and fidelity for the insertion of correct dCTP, with respect to the other incorrect nucleotides, opposite the adduct of AMD, was investigated. For a deeper understanding of the factors that control the bypass of the site-specific adducts of AMD catalyzed by DNA polymerases, we also used microscale thermophoresis (MST) to measure the thermodynamic changes associated with TLS across a single, site-specific adduct formed in DNA by AMD. The relative catalytic efficiency of the investigated DNA polymerases for the insertion of correct dCTP, with respect to the other incorrect nucleotides, opposite the AMD adduct, was reduced. Nevertheless, incorporation of the correct C opposite the G modified by AMD of the template strand was promoted by an increasing thermodynamic stability of the resulting duplex. The reduced relative efficiency of the investigated DNA polymerases may be a consequence of the DNA intercalation of the acridine moiety of AMD and the size of the adduct. The products of the bypass of this monofunctional lesion produced by AMD and DNA polymerases also resulted from the misincorporation of dNTPs opposite the platinated G residues. The MST analysis suggested that thermodynamic factors may contribute to the forces that governed enhanced incorporation of the incorrect dNTPs by DNA polymerases.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21019964
- 003
- CZ-PrNML
- 005
- 20210830101548.0
- 007
- ta
- 008
- 210728s2020 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/ijms21207806 $2 doi
- 035 __
- $a (PubMed)33096927
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Hreusova, Monika $u Czech Academy of Sciences, Institute of Biophysics, Kralovopolska 135, CZ-61265 Brno, Czech Republic $u Department of Biophysics, Faculty of Science, Palacky University, Slechtitelu 27, CZ 78371 Olomouc, Czech Republic
- 245 10
- $a Thermodynamic Insights by Microscale Thermophoresis into Translesion DNA Synthesis Catalyzed by DNA Polymerases Across a Lesion of Antitumor Platinum-Acridine Complex / $c M. Hreusova, O. Novakova, V. Brabec
- 520 9_
- $a Translesion synthesis (TLS) through DNA adducts of antitumor platinum complexes has been an interesting aspect of DNA synthesis in cells treated with these metal-based drugs because of its correlation to drug sensitivity. We utilized model systems employing a DNA lesion derived from a site-specific monofunctional adduct formed by antitumor [PtCl(en)(L)](NO3)2 (complex AMD, en = ethane-1,2-diamine, L = N-[2-(acridin-9-ylamino)ethyl]-N-methylpropionamidine) at a unique G residue. The catalytic efficiency of TLS DNA polymerases, which differ in their processivity and fidelity for the insertion of correct dCTP, with respect to the other incorrect nucleotides, opposite the adduct of AMD, was investigated. For a deeper understanding of the factors that control the bypass of the site-specific adducts of AMD catalyzed by DNA polymerases, we also used microscale thermophoresis (MST) to measure the thermodynamic changes associated with TLS across a single, site-specific adduct formed in DNA by AMD. The relative catalytic efficiency of the investigated DNA polymerases for the insertion of correct dCTP, with respect to the other incorrect nucleotides, opposite the AMD adduct, was reduced. Nevertheless, incorporation of the correct C opposite the G modified by AMD of the template strand was promoted by an increasing thermodynamic stability of the resulting duplex. The reduced relative efficiency of the investigated DNA polymerases may be a consequence of the DNA intercalation of the acridine moiety of AMD and the size of the adduct. The products of the bypass of this monofunctional lesion produced by AMD and DNA polymerases also resulted from the misincorporation of dNTPs opposite the platinated G residues. The MST analysis suggested that thermodynamic factors may contribute to the forces that governed enhanced incorporation of the incorrect dNTPs by DNA polymerases.
- 650 _2
- $a akridiny $x chemie $x farmakologie $7 D000166
- 650 _2
- $a biokatalýza $7 D055162
- 650 _2
- $a katalýza $7 D002384
- 650 _2
- $a DNA $x biosyntéza $7 D004247
- 650 _2
- $a adukty DNA $x chemie $x genetika $x metabolismus $7 D018736
- 650 _2
- $a oprava DNA $7 D004260
- 650 _2
- $a replikace DNA $7 D004261
- 650 _2
- $a DNA-dependentní DNA-polymerasy $x metabolismus $7 D004259
- 650 _2
- $a guanin $x metabolismus $7 D006147
- 650 _2
- $a nukleotidy $x genetika $x metabolismus $7 D009711
- 650 _2
- $a sloučeniny platiny $x chemie $x farmakologie $7 D017671
- 650 _2
- $a tepelná difuze $7 D055471
- 650 _2
- $a termodynamika $7 D013816
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Novakova, Olga $u Czech Academy of Sciences, Institute of Biophysics, Kralovopolska 135, CZ-61265 Brno, Czech Republic
- 700 1_
- $a Brabec, Viktor $u Czech Academy of Sciences, Institute of Biophysics, Kralovopolska 135, CZ-61265 Brno, Czech Republic
- 773 0_
- $w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 21, č. 20 (2020)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33096927 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20210830101548 $b ABA008
- 999 __
- $a ok $b bmc $g 1690703 $s 1140410
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 21 $c 20 $e 20201021 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
- GRA __
- $a 18-09502S $p Grantová Agentura České Republiky
- LZP __
- $a Pubmed-20210728