Literature DB >> 7838711

The solution structure of a 3'-phenazinium (Pzn) tethered DNA-RNA duplex with a dangling adenosine: r(5'G-AUUGAA3'):d(5'TCAATC3'-Pzn).

T V Maltseva1, P Agback, M N Repkova, A G Venyaminova, E M Ivanova, A Sandström, V F Zarytova, J Chattopadhyaya.   

Abstract

The 3'-Pzn group tethered to an oligo-DNA stabilizes a DNA-RNA hybrid duplex structure by 13 degrees C compared to the natural counterpart. This report constitutes the first full study of the conformational features of a hybrid DNA-RNA duplex, which has been possible because of the unique stabilization of this rather small duplex by the tethered 3'-Pzn moiety (Tm approximately 40 degrees C from NMR). In this study, a total of 252 inter- and intra-strand torsional and distance constraints along with the full NOE relaxation matrix, taking into account the exchange process of imino and amino protons with water, have been used. The 3'-Pzn-promoted stabilization of the DNA-RNA hybrid duplex results in detailed local conformational characteristics such as the torsion angles of the backbone and sugar moieties that are close to the features of the other natural DNA-RNA hybrids (i.e. sugars of the RNA strand are 3'-endo, but the sugars of the DNA strand are intermediate between A- and B-forms of DNA, 72 degrees < P < 180 degrees; note however, that the sugars of our DNA strand have a C1-exo conformation: 131 degrees < P < 154 degrees). This study suggests that 3'-Pzn-tethered smaller oligo-DNA should serve the same purpose as a larger oligo-DNA as a antisense inhibitor of the viral mRNA. Additionally, these types of tethered oligos have been found to be relatively more resistant to the cellular nuclease. Moreover, they are taken up quite readily through the cellular membrane (14) compared to the natural counterparts.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7838711      PMCID: PMC310121          DOI: 10.1093/nar/22.25.5590

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


  20 in total

1.  Determination of nucleic acid backbone conformation by 1H NMR.

Authors:  S G Kim; L J Lin; B R Reid
Journal:  Biochemistry       Date:  1992-04-14       Impact factor: 3.162

2.  Errors in RNA NOESY distance measurements in chimeric and hybrid duplexes: differences in RNA and DNA proton relaxation.

Authors:  A C Wang; S G Kim; P F Flynn; S H Chou; J Orban; B R Reid
Journal:  Biochemistry       Date:  1992-04-28       Impact factor: 3.162

3.  [Automated H-phosphonate synthesis of oligoribonucleotides using 2'-O-tetrahydropyranyl protective group].

Authors:  A G Ven'iaminova; V V Gorn; M A Zenkova; N I Komarova; M N Repkova
Journal:  Bioorg Khim       Date:  1990-07

4.  Structural study of a DNA.RNA hybrid duplex with a chiral phosphorothioate moiety by NMR: extraction of distance and torsion angle constraints and imino proton exchange rates.

Authors:  C González; W Stec; A Kobylanska; R I Hogrefe; M Reynolds; T L James
Journal:  Biochemistry       Date:  1994-09-20       Impact factor: 3.162

5.  The search for structure-specific nucleic acid-interactive drugs: effects of compound structure on RNA versus DNA interaction strength.

Authors:  W D Wilson; L Ratmeyer; M Zhao; L Strekowski; D Boykin
Journal:  Biochemistry       Date:  1993-04-20       Impact factor: 3.162

6.  Solution structure of the parallel-stranded duplex oligonucleotide alpha-d(TCTAAAC)-beta-d(AGATTTG) via complete relaxation matrix analysis of the NOE effects and molecular mechanics calculations.

Authors:  G Lancelot; J L Guesnet; F Vovelle
Journal:  Biochemistry       Date:  1989-09-19       Impact factor: 3.162

7.  NMR assignments and solution conformation of the DNA.RNA hybrid duplex d(GTGAACTT).r(AAGUUCAC).

Authors:  A N Lane; S Ebel; T Brown
Journal:  Eur J Biochem       Date:  1993-07-15

8.  Preparative solid phase synthesis of a tetradecamer r(GAUUGAAAAUCCCC) by the H-phosphonate method using a 2'-O-tetrahydropyranyl protective group.

Authors:  A G Venyaminova; M N Repkova; T V Maltseva
Journal:  Nucleic Acids Symp Ser       Date:  1991

9.  Synthesis and high stability of complementary complexes of N-(2-hydroxyethyl)phenazinium derivatives of oligonucleotides.

Authors:  S G Lokhov; M A Podyminogin; D S Sergeev; V N Silnikov; I V Kutyavin; G V Shishkin; V P Zarytova
Journal:  Bioconjug Chem       Date:  1992 Sep-Oct       Impact factor: 4.774

10.  [Study of the spatial structure of the duplex (Phn-NH(CH2)NH)pd(CCAAACA).pd(TGTTTGGC) with covalently bound 10-(2-hydroxyethyl)phenazine by in aqueous solution by 2D-(1)H-NMR and by limited molecular mechanics].

Authors:  E V Bichenkova; L A Gorenshteĭn; Iu N Vorob'ev; E Iu Tenne; V F Zarytova; E M Ivanova; T V Mal'tseva; A V Lebedev
Journal:  Bioorg Khim       Date:  1992-07
View more
  2 in total

1.  The solution structure of [d(CGC)r(aaa)d(TTTGCG)](2): hybrid junctions flanked by DNA duplexes.

Authors:  S T Hsu; M T Chou; J W Cheng
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

2.  The dependence of DNase I activity on the conformation of oligodeoxynucleotides.

Authors:  D H Sutton; G L Conn; T Brown; A N Lane
Journal:  Biochem J       Date:  1997-01-15       Impact factor: 3.857

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.