Literature DB >> 12763313

Interactions of cryptolepine and neocryptolepine with unusual DNA structures.

Lionel Guittat1, Patrizia Alberti, Frédéric Rosu, Sabine Van Miert, Emilie Thetiot, Luc Pieters, Valérie Gabelica, Edwin De Pauw, Alexandre Ottaviani, Jean-François Riou, Jean-Louis Mergny.   

Abstract

Cryptolepine, the main alkaloid present in the roots of Cryptolepis sanguinolenta, presents a large spectrum of biological properties. It has been reported to behave like a DNA intercalator with a preference for GC-rich sequences. In this study, dialysis competition assay and mass spectrometry experiments were used to determine the affinity of cryptolepine and neocryptolepine for DNA structures among duplexes, triplexes, quadruplexes and single strands. Our data confirm that cryptolepine and neocryptolepine prefer GC over AT-rich duplex sequences, but also recognize triplex and quadruplex structures. These compounds are weak telomerase inhibitors and exhibit a significant preference for triplexes over quadruplexes or duplexes.

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Year:  2003        PMID: 12763313     DOI: 10.1016/s0300-9084(03)00035-x

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  30 in total

1.  Gas-phase stability of G-quadruplex DNA determined by electrospray ionization tandem mass spectrometry and molecular dynamics simulations.

Authors:  Carolyn L Mazzitelli; Junmei Wang; Suncerae I Smith; Jennifer S Brodbelt
Journal:  J Am Soc Mass Spectrom       Date:  2007-07-17       Impact factor: 3.109

2.  ESI-MS characterization of a novel pyrrole-inosine nucleoside that interacts with guanine bases.

Authors:  Sarah E Pierce; Courtney L Sherman; Janarthanan Jayawickramarajah; Candace M Lawrence; Jonathan L Sessler; Jennifer S Brodbelt
Journal:  Anal Chim Acta       Date:  2008-04-15       Impact factor: 6.558

3.  Synthesis of naphthalimide derivatives with potential anticancer activity, their comparative ds- and G-quadruplex-DNA binding studies and related biological activities.

Authors:  Ufuk Yildiz; Irfan Kandemir; Füsun Cömert; Senem Akkoç; Burak Coban
Journal:  Mol Biol Rep       Date:  2020-02-25       Impact factor: 2.316

4.  Evaluation of binding of perylene diimide and benzannulated perylene diimide ligands to DNA by electrospray ionization mass spectrometry.

Authors:  Carolyn L Mazzitelli; Jennifer S Brodbelt; Jonathan T Kern; Mireya Rodriguez; Sean M Kerwin
Journal:  J Am Soc Mass Spectrom       Date:  2006-02-28       Impact factor: 3.109

5.  Identification of 3-phenylaminoquinolinium and 3-phenylaminopyridinium salts as new agents against opportunistic fungal pathogens.

Authors:  Tryphon K Mazu; Jagan R Etukala; Xue Y Zhu; Melissa R Jacob; Shabana I Khan; Larry A Walker; Seth Y Ablordeppey
Journal:  Bioorg Med Chem       Date:  2010-11-05       Impact factor: 3.641

6.  Characterization of the cytotoxic activity of the indoloquinoline alkaloid cryptolepine in human tumour cell lines and primary cultures of tumour cells from patients.

Authors:  Daniel Laryea; Anders Isaksson; Colin W Wright; Rolf Larsson; Peter Nygren
Journal:  Invest New Drugs       Date:  2008-10-14       Impact factor: 3.850

7.  Interactions of sulfur-containing acridine ligands with DNA by ESI-MS.

Authors:  Suncerae I Smith; Frank S Guziec; Lynn Guziec; Jennifer S Brodbelt
Journal:  Analyst       Date:  2009-08-25       Impact factor: 4.616

8.  Ligand binding mode to duplex and triplex DNA assessed by combining electrospray tandem mass spectrometry and molecular modeling.

Authors:  Frédéric Rosu; Chi-Hung Nguyen; Edwin De Pauw; Valérie Gabelica
Journal:  J Am Soc Mass Spectrom       Date:  2007-03-28       Impact factor: 3.109

9.  Antioxidative, antimicrobial and cytotoxic effects of the phenolics of Leea indica leaf extract.

Authors:  Md Atiar Rahman; Talha Bin Imran; Shahidul Islam
Journal:  Saudi J Biol Sci       Date:  2012-12-20       Impact factor: 4.219

Review 10.  Indolo[3,2-b]quinolines: synthesis, biological evaluation and structure activity-relationships.

Authors:  Eyunni V K Suresh Kumar; Jagan R Etukala; Seth Y Ablordeppey
Journal:  Mini Rev Med Chem       Date:  2008-06       Impact factor: 3.862

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