Literature DB >> 22183179

Natural product DNA major groove binders.

Paris L Hamilton1, Dev P Arya.   

Abstract

Covering: 1980 to 2011. Major groove recognition of DNA by proteins utilizes the variation in hydrogen bond donor/acceptor content that makes DNA base-pairs distinguishable from one another. Specific ligand-DNA interactions in the major groove are necessary to develop approaches for inhibition of DNA-protein interactions. As opposed to minor groove binders, little research has been achieved in recognition of the DNA major groove. This review summarizes the progress in identification of natural products that bind to the major groove of DNA. We first review the natural products, pluramycins, aflatoxins, azinomycins, leinamycin, neocarzinostatin, and ditercalinium, that are known to possess major groove interacting elements. These compounds, however, interact primarily with DNA by intercalation between base-pair steps. Some of these compounds utilize non-covalent interactions in order to position themselves to alkylate DNA at the nucleophilic N7 positions on nearby purine bases. Finally, recent reports of non-covalent major groove binding with carbohydrates, aminoglycosides in particular, have revealed them as promising leads for DNA major groove binding probes or drugs.

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Year:  2011        PMID: 22183179     DOI: 10.1039/c1np00054c

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  29 in total

1.  Click dimers to target HIV TAR RNA conformation.

Authors:  Sunil Kumar; Patrick Kellish; W Edward Robinson; Deyun Wang; Daniel H Appella; Dev P Arya
Journal:  Biochemistry       Date:  2012-03-09       Impact factor: 3.162

Review 2.  p53 and RAD9, the DNA Damage Response, and Regulation of Transcription Networks.

Authors:  Howard B Lieberman; Sunil K Panigrahi; Kevin M Hopkins; Li Wang; Constantinos G Broustas
Journal:  Radiat Res       Date:  2017-01-31       Impact factor: 2.841

3.  Structural characterization of O- and C-glycosylating variants of the landomycin glycosyltransferase LanGT2.

Authors:  Heng Keat Tam; Johannes Härle; Stefan Gerhardt; Jürgen Rohr; Guojun Wang; Jon S Thorson; Aurélien Bigot; Monika Lutterbeck; Wolfgang Seiche; Bernhard Breit; Andreas Bechthold; Oliver Einsle
Journal:  Angew Chem Int Ed Engl       Date:  2015-01-07       Impact factor: 15.336

4.  Recognition of double-stranded DNA using energetically activated duplexes with interstrand zippers of 1-, 2- or 4-pyrenyl-functionalized O2'-alkylated RNA monomers.

Authors:  Saswata Karmakar; Andreas S Madsen; Dale C Guenther; Bradley C Gibbons; Patrick J Hrdlicka
Journal:  Org Biomol Chem       Date:  2014-08-21       Impact factor: 3.876

Review 5.  DNA Recognition by a Novel Bis-Intercalator, Potent Anticancer Drug XR5944.

Authors:  Clement Lin; Danzhou Yang
Journal:  Curr Top Med Chem       Date:  2015       Impact factor: 3.295

6.  Influence of linker length in shape recognition of B* DNA by dimeric aminoglycosides.

Authors:  Sunil Kumar; Meredith Newby Spano; Dev P Arya
Journal:  Bioorg Med Chem       Date:  2015-05-08       Impact factor: 3.641

7.  Dimeric and trimeric derivatives of the azinomycin B chromophore show enhanced DNA binding.

Authors:  Milena Balazy; Alejandra Fausto; Christina Voskanian; Bianca Chavez; Harmanpreet Panesar; Thomas G Minehan
Journal:  Org Biomol Chem       Date:  2017-05-31       Impact factor: 3.876

8.  Shape readout of AT-rich DNA by carbohydrates.

Authors:  Sunil Kumar; Meredith Newby Spano; Dev P Arya
Journal:  Biopolymers       Date:  2014-07       Impact factor: 2.505

Review 9.  Binding to the DNA minor groove by heterocyclic dications: from AT-specific monomers to GC recognition with dimers.

Authors:  Rupesh Nanjunda; W David Wilson
Journal:  Curr Protoc Nucleic Acid Chem       Date:  2012-12

10.  Recognition of mixed-sequence DNA duplexes: design guidelines for invaders based on 2'-O-(pyren-1-yl)methyl-RNA monomers.

Authors:  Saswata Karmakar; Dale C Guenther; Patrick J Hrdlicka
Journal:  J Org Chem       Date:  2013-11-20       Impact factor: 4.354

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