Literature DB >> 6661418

Two-dimensional proton nuclear magnetic resonance investigation of the synthetic deoxyribonucleic acid decamer d(ATATCGATAT)2.

J Feigon, W Leupin, W A Denny, D R Kearns.   

Abstract

In this study two-dimensional NMR techniques (COSY and NOESY) have been used in conjunction with one-dimensional NMR results to complete the assignment of the proton NMR spectrum of the double-stranded DNA decamer, d(ATATCGATAT)2, and to obtain qualitative information about numerous interproton distances in this molecule and some limited information about conformational dynamics. COSY and NOESY measurements have been combined to systematically assign many of the resonances from the H1' and H2',2" sugar protons to specific nucleotides in the double helix. This method relies on the fact that sugar protons within a specific nucleotide are scalar coupled and that base protons (AH8, GH8, TH6, and CH6) in right-handed helices can interact simultaneously with their own H2',2" sugar protons and those of the adjacent (5'-3') nucleotide attached to its 5' side (i.e., XpA not ApX). A COSY experiment is used to identify sugar resonances within a residue whereas the NOESY experiment allows the neighboring sugar to be connected (linked). The CH5 and CH6 resonances in the spectrum can immediately be identified by the COSY experiment. The methyl protons of thymine residues exhibit strong through-space interbase interactions both with their own TH6 proton and with AH8 proton on the adjacent (5'-3') adenine residue. These interactions are used both to make assignments of the spectra and to establish that the thymine methyl groups are in close proximity to the AH8 protons of adjacent adenine residues [Feigon, J., Wright, J. M., Leupin, W., Denny, W. A., & Kearns, D. R. (1982) J. Am. Chem. Soc. 104, 5540].(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1983        PMID: 6661418     DOI: 10.1021/bi00294a038

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  39 in total

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Authors:  M Ghosh; N Vinay Kumar; U Varshney; K V Chary
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2.  NMR structure of an alpha-L-LNA:RNA hybrid: structural implications for RNase H recognition.

Authors:  Jakob T Nielsen; Paul C Stein; Michael Petersen
Journal:  Nucleic Acids Res       Date:  2003-10-15       Impact factor: 16.971

3.  Assignment methodology for larger RNA oligonucleotides: application to an ATP-binding RNA aptamer.

Authors:  T Dieckmann; J Feigon
Journal:  J Biomol NMR       Date:  1997-04       Impact factor: 2.835

4.  An NMR structural study of deaminated base pairs in DNA.

Authors:  C Carbonnaux; G V Fazakerley; L C Sowers
Journal:  Nucleic Acids Res       Date:  1990-07-25       Impact factor: 16.971

5.  Proton NMR study of the [d(ACGTATACGT)]2-2echinomycin complex: conformational changes between echinomycin binding sites.

Authors:  D E Gilbert; J Feigon
Journal:  Nucleic Acids Res       Date:  1992-05-25       Impact factor: 16.971

6.  Comparison of the conformation of an oligonucleotide containing a central G-T base pair with the non-mismatch sequence by proton NMR.

Authors:  E Quignard; G V Fazakerley; G van der Marel; J H van Boom; W Guschlbauer
Journal:  Nucleic Acids Res       Date:  1987-04-24       Impact factor: 16.971

7.  Two-dimensional NMR investigation of a bent DNA fragment: assignment of the proton resonances and preliminary structure analysis.

Authors:  A Kintanar; R E Klevit; B R Reid
Journal:  Nucleic Acids Res       Date:  1987-07-24       Impact factor: 16.971

8.  Study of structure, base-pair opening kinetics and proton exchange mechanism of the d-(AATTGCAATT) self-complementary oligodeoxynucleotide in solution.

Authors:  M Kochoyan; G Lancelot; J L Leroy
Journal:  Nucleic Acids Res       Date:  1988-08-11       Impact factor: 16.971

9.  Solution structure of oligonucleotides covalently linked to a psoralen derivative.

Authors:  O Bornet; C Prévost; F Vovelle; M Chassignol; N T Thuong; G Lancelot
Journal:  Nucleic Acids Res       Date:  1995-03-11       Impact factor: 16.971

10.  alpha-DNA-V. Parallel annealing, handedness and conformation of the duplex of the unnatural alpha-hexadeoxyribonucleotide alpha-[d(CpApTpGpCpG)] with its beta-complement beta-[d(GpTpApCpGpC)] deduced from high field 1H-NMR.

Authors:  F Morvan; B Rayner; J L Imbach; M Lee; J A Hartley; D K Chang; J W Lown
Journal:  Nucleic Acids Res       Date:  1987-09-11       Impact factor: 16.971

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