Literature DB >> 6166855

[Mechanism of AT base pairs recognition by molecules of dye "Hoechst 33258"].

M V Mikhaĭlov, A S Zasedatelev, A S Krylov, G V Gurskiĭ.   

Abstract

Experimental studies are reported on the binding of the dye "Hoechst 33 258" to DNA and synthetic polynucleotides. A stereochemical model of binding of the dye to DNA is proposed. According to the model, the molecules of the dye are located in the minor groove of DNA, each covering 4 base pairs. The benzimidazole backbone of the dye tends to form a helix isogeometric to that of DNA in the B form. The specifisity of "Hoechst 33 258" binding to At pairs involves hydrogen bonding of two NH-groups of benzimidazole rings and CH3N+H group of the piperazine ring to O2 oxygenes of thymines and N3 nitrogens of adenines facing the minor groove of the DNA double helix.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 6166855

Source DB:  PubMed          Journal:  Mol Biol (Mosk)        ISSN: 0026-8984


  3 in total

1.  Binding of the Hoechst 33342 dye in the monomer and sandwich form with poly[d(AT)].poly[d(AT)] and the self-complementary dodecamer 5'-CGTATATATACG-3'.

Authors:  S A Rodin; V F Pis'menskii; A M Nikitin; A N Surovaya; G V Gursky
Journal:  Dokl Biochem Biophys       Date:  2001 Jul-Aug       Impact factor: 0.788

2.  Ensemble and single-molecule fluorescence spectroscopic study of the binding modes of the bis-benzimidazole derivative Hoechst 33258 with DNA.

Authors:  Amitava Adhikary; Volker Buschmann; Christian Müller; Markus Sauer
Journal:  Nucleic Acids Res       Date:  2003-04-15       Impact factor: 16.971

3.  Identification of small molecule and genetic modulators of AON-induced dystrophin exon skipping by high-throughput screening.

Authors:  Debra A O'Leary; Orzala Sharif; Paul Anderson; Buu Tu; Genevieve Welch; Yingyao Zhou; Jeremy S Caldwell; Ingo H Engels; Achim Brinker
Journal:  PLoS One       Date:  2009-12-17       Impact factor: 3.240

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.