Literature DB >> 7651830

UV spectroscopic identification and thermodynamic analysis of protonated third strand deoxycytidine residues at neutrality in the triplex d(C(+)-T)6:[d(A-G)6.d(C-T)6]; evidence for a proton switch.

L Lavelle1, J R Fresco.   

Abstract

Near-UV difference spectral analysis of the triplex formed from d(C-T)6 and d(A-G)6.d(C-T)6 in neutral and acidic solution shows that the third strand dC residues are protonated at pH 7.0, far above their intrinsic pKa. Additional support for ion-dipole interactions between the third strand dC residues and the G.C target base pairs comes from reduced positive dependence of triplet stability on ionic strength below 0.9 M Na+, inverse dependence above 0.9 M Na+ and strong positive dependence on hydrogen ion concentration. Molecular modeling (AMBER) of C:G.C and C+:G.C base triplets with the third strand base bound in the Hoogsteen geometry shows that only the C+:G.C triplet is energetically feasible. van't Hoff analysis of the melting of the triplex and target duplex shows that between pH 5.0 and 8.5 in 0.15 M NaCl/0.005 M MgCl2 the enthalpy of melting (delta H degree obs) varies from 5.7 to 6.6 kcal.mol-1 for the duplex in a duplex mixture and from 7.3 to 9.7 kcal.mol-1 for third strand dissociation in the triplex mixture. We have extended the condensation-screening theory of Manning to pH-dependent third strand binding. In this development we explicitly include the H+ contribution to the electrostatic free energy and obtain [formula: see text]. The number of protons released in the dissociation of the third strand from the target duplex at pH 7.0, delta n2, is thereby calculated to be 5.5, in good agreement with approximately six third strand dc residues per mole of triplex. This work shows that when third strand binding requires protonated residues that would otherwise be neutral, triplex formation and dissociation are mediated by proton uptake and release, i.e., a proton switch. As a by-product of this study, we have found that at low pH the Watson-Crick duplex d(A-G)6.d(C-T)6 undergoes a transition to a parallel Hoogsteen duplex d(A-G)6.d(C(+)-T)6.

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Year:  1995        PMID: 7651830      PMCID: PMC307094          DOI: 10.1093/nar/23.14.2692

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  49 in total

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4.  Interaction of an N-methylated polyamine analogue, hexamethonium(2+), with NaDNA: quantitative 14N and 23Na NMR relaxation rate studies of the cation-exchange process.

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Journal:  Biochemistry       Date:  1988-06-14       Impact factor: 3.162

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Journal:  FASEB J       Date:  1988-11       Impact factor: 5.191

8.  Triple helix formation by oligopurine-oligopyrimidine DNA fragments. Electrophoretic and thermodynamic behavior.

Authors:  G Manzini; L E Xodo; D Gasparotto; F Quadrifoglio; G A van der Marel; J H van Boom
Journal:  J Mol Biol       Date:  1990-06-20       Impact factor: 5.469

9.  Formation of a stable triplex from a single DNA strand.

Authors:  V Sklenár; J Feigon
Journal:  Nature       Date:  1990-06-28       Impact factor: 49.962

10.  NMR studies of pH-dependent conformational polymorphism of alternating (C-T)n sequences.

Authors:  T N Jaishree; A H Wang
Journal:  Nucleic Acids Res       Date:  1993-08-11       Impact factor: 16.971

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  13 in total

1.  Use of a pyrimidine nucleoside that functions as a bidentate hydrogen bond donor for the recognition of isolated or contiguous G-C base pairs by oligonucleotide-directed triplex formation.

Authors:  G Xiang; R Bogacki; L W McLaughlin
Journal:  Nucleic Acids Res       Date:  1996-05-15       Impact factor: 16.971

2.  Evaluation of pyrimidine PNA binding to ssDNA targets from nonequilibrium melting experiments.

Authors:  E A Lesnik; L M Risen; D A Driver; M C Griffith; K Sprankle; S M Freier
Journal:  Nucleic Acids Res       Date:  1997-02-01       Impact factor: 16.971

3.  Effect of third strand composition on the triple helix formation: purine versus pyrimidine oligodeoxynucleotides.

Authors:  B Faucon; J L Mergny; C Héléne
Journal:  Nucleic Acids Res       Date:  1996-08-15       Impact factor: 16.971

4.  Optimal design of parallel triplex forming oligonucleotides containing Twisted Intercalating Nucleic Acids--TINA.

Authors:  Uffe V Schneider; Nikolaj D Mikkelsen; Nina Jøhnk; Limei M Okkels; Henrik Westh; Gorm Lisby
Journal:  Nucleic Acids Res       Date:  2010-03-24       Impact factor: 16.971

5.  Triplex formation by a psoralen-conjugated oligodeoxyribonucleotide containing the base analog 8-oxo-adenine.

Authors:  P S Miller; G Bi; S A Kipp; V Fok; R K DeLong
Journal:  Nucleic Acids Res       Date:  1996-02-15       Impact factor: 16.971

6.  Hoogsteen-paired homopurine [RP-PS]-DNA and homopyrimidine RNA strands form a thermally stable parallel duplex.

Authors:  Piotr Guga; Magdalena Janicka; Anna Maciaszek; Beata Rebowska; Genowefa Nowak
Journal:  Biophys J       Date:  2007-08-10       Impact factor: 4.033

7.  Triplex formation at physiological pH by 5-Me-dC-N4-(spermine) [X] oligodeoxynucleotides: non protonation of N3 in X of X*G:C triad and effect of base mismatch/ionic strength on triplex stabilities.

Authors:  D A Barawkar; K G Rajeev; V A Kumar; K N Ganesh
Journal:  Nucleic Acids Res       Date:  1996-04-01       Impact factor: 16.971

8.  Stabilization of unstable CGC+ triplex DNA by single-walled carbon nanotubes under physiological conditions.

Authors:  Yujun Song; Lingyan Feng; Jinsong Ren; Xiaogang Qu
Journal:  Nucleic Acids Res       Date:  2011-05-16       Impact factor: 16.971

Review 9.  Molecular basis for chiral selection in RNA aminoacylation.

Authors:  Koji Tamura
Journal:  Int J Mol Sci       Date:  2011-07-22       Impact factor: 5.923

10.  Structural properties and gene-silencing activity of chemically modified DNA-RNA hybrids with parallel orientation.

Authors:  Maryam Habibian; Maryam Yahyaee-Anzahaee; Matije Lucic; Elena Moroz; Nerea Martín-Pintado; Logan Dante Di Giovanni; Jean-Christophe Leroux; Jonathan Hall; Carlos González; Masad J Damha
Journal:  Nucleic Acids Res       Date:  2018-02-28       Impact factor: 16.971

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