JAROŠOVÁ, Petra, Roman SÁNDOR, Andrea SLANINKOVÁ, Marek VIDO, Ondřej PEŠ and Petr TÁBORSKÝ. Quaternary protoberberine alkaloids and their interactions with DNA. Chemical Papers. CHAM: SPRINGER INTERNATIONAL PUBLISHING AG, 2019, vol. 73, No 12, p. 2965-2973. ISSN 0366-6352. Available from: https://dx.doi.org/10.1007/s11696-019-00857-z.
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Basic information
Original name Quaternary protoberberine alkaloids and their interactions with DNA
Authors JAROŠOVÁ, Petra (203 Czech Republic, belonging to the institution), Roman SÁNDOR (703 Slovakia, belonging to the institution), Andrea SLANINKOVÁ (703 Slovakia, belonging to the institution), Marek VIDO (703 Slovakia, belonging to the institution), Ondřej PEŠ (203 Czech Republic, belonging to the institution) and Petr TÁBORSKÝ (203 Czech Republic, guarantor, belonging to the institution).
Edition Chemical Papers, CHAM, SPRINGER INTERNATIONAL PUBLISHING AG, 2019, 0366-6352.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10406 Analytical chemistry
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 0.963 in 2017
RIV identification code RIV/00216224:14310/19:00112242
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1007/s11696-019-00857-z
UT WoS 000488930200010
Keywords in English Protoberberine alkaloids; Non-canonical structures; G-quadruplex; dsDNA; Competitive dialysis; CD; Melting temperatures; Mass spectrometry
Tags 14110512, CF BIC, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 11/5/2020 17:31.
Abstract
The G-quadruplex DNA is commonly present in several protooncogenic-DNA promoters and participates in many important biological processes such as replication, transcription, and translation. Because of their supposed role in cancer, G-quadruplex DNA is often studied as a target for anti-cancer drugs. Quaternary protoberberine and tetrahydroprotoberberine alkaloids (corysamine, coptisine, stylopine), which are supposed to selectively bind these structures, have been compared in terms of stability with selected types of DNA. Influence of selected alkaloids on the stability of double-stranded DNA and non-canonical forms of DNA was observed by determining association constants of alkaloid-DNA complexes using spectroscopic methods-molecular absorption spectrometry, fluorescence spectrometry, and mass spectrometry. Furthermore, the effect of given alkaloids on the melting temperature of these DNA structures was determined using CD spectrometry. Competitive dialysis and electrospray mass spectrometry were performed for affinity comparison of certain alkaloids to different DNA structures including G-quadruplexes. These experiments have proven that corysamine and coptisine prefer interaction with G-quadruplexes in comparison to dsDNA and ssDNA, whereas tetrahydroprotoberberine alkaloid stylopine does not interact with any DNA whatsoever.
Links
ED1.1.00/02.0068, research and development projectName: CEITEC - central european institute of technology
MUNI/A/0976/2018, interní kód MUName: Příspěvek chemických a biochemických metodik ke studiu molekulární podstaty vybraných patologických stavů a onemocnění
Investor: Masaryk University, Category A
MUNI/A/1286/2017, interní kód MUName: Vývoj metod a instrumentace pro analýzu biologicky významných látek 2018
Investor: Masaryk University, Category A
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