1tne

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(New page: 200px<br /><applet load="1tne" size="450" color="white" frame="true" align="right" spinBox="true" caption="1tne" /> '''NMR STUDY OF Z-DNA AT PHYSIOLOGICAL SALT CON...)
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'''NMR STUDY OF Z-DNA AT PHYSIOLOGICAL SALT CONDITIONS, MINIMIZED AVERAGE STRUCTURE'''<br />
'''NMR STUDY OF Z-DNA AT PHYSIOLOGICAL SALT CONDITIONS, MINIMIZED AVERAGE STRUCTURE'''<br />
==Overview==
==Overview==
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Various oligonucleotides containing 8-methylguanine (m8G) have been, synthesized and their structures and thermodynamic properties, investigated. Introduction Of M8G into DNA sequences markedly stabilizes, the Z conformation under low salt conditions. The hexamer d(CGC[M8G]CG)2, exhibits a CD spectrum characteristic of the Z conformation under, physiological salt conditions. The NOE-restrained refinement unequivocally, demonstrated that d(CGC[m8G]CG)2 adopts a Z structure with all guanines in, the syn conformation. The refined NMR structure is very similar to the Z, form crystal structure of d(CGCGCG)2, with a root mean square deviation of, 0.6 between the two structures. The contribution of m8G to the, stabilization of Z-DNA has been estimated from the mid-point NaCl, concentrations for the B-Z transition of various m8G-containing oligomers., The presence of m8G in d(CGC[m8G]CG)2 stabilizes the Z conformation by at, least deltaG = -0.8 kcal/mol relative to the unmodified hexamer. The Z, conformation was further stabilized by increasing the number of m8Gs, incorporated and destabilized by incorporating syn-A or syn-T, found, respectively in the (A,T)-containing alternating and non-alternating, pyrimidine-purine sequences. The results suggest that the chemically less, reactive m8G base is a useful agent for studying molecular interactions of, Z-DNA or other DNA structures that incorporate syn-G conformation.
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Various oligonucleotides containing 8-methylguanine (m8G) have been synthesized and their structures and thermodynamic properties investigated. Introduction Of M8G into DNA sequences markedly stabilizes the Z conformation under low salt conditions. The hexamer d(CGC[M8G]CG)2 exhibits a CD spectrum characteristic of the Z conformation under physiological salt conditions. The NOE-restrained refinement unequivocally demonstrated that d(CGC[m8G]CG)2 adopts a Z structure with all guanines in the syn conformation. The refined NMR structure is very similar to the Z form crystal structure of d(CGCGCG)2, with a root mean square deviation of 0.6 between the two structures. The contribution of m8G to the stabilization of Z-DNA has been estimated from the mid-point NaCl concentrations for the B-Z transition of various m8G-containing oligomers. The presence of m8G in d(CGC[m8G]CG)2 stabilizes the Z conformation by at least deltaG = -0.8 kcal/mol relative to the unmodified hexamer. The Z conformation was further stabilized by increasing the number of m8Gs incorporated and destabilized by incorporating syn-A or syn-T, found respectively in the (A,T)-containing alternating and non-alternating pyrimidine-purine sequences. The results suggest that the chemically less reactive m8G base is a useful agent for studying molecular interactions of Z-DNA or other DNA structures that incorporate syn-G conformation.
==About this Structure==
==About this Structure==
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1TNE is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1TNE OCA].
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1TNE is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1TNE OCA].
==Reference==
==Reference==
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[[Category: Saito, I.]]
[[Category: Saito, I.]]
[[Category: Sugiyama, H.]]
[[Category: Sugiyama, H.]]
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[[Category: Wang, A.H.J.]]
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[[Category: Wang, A H.J.]]
[[Category: z-dna]]
[[Category: z-dna]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:27:09 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:15:23 2008''

Revision as of 13:15, 21 February 2008


1tne

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NMR STUDY OF Z-DNA AT PHYSIOLOGICAL SALT CONDITIONS, MINIMIZED AVERAGE STRUCTURE

Overview

Various oligonucleotides containing 8-methylguanine (m8G) have been synthesized and their structures and thermodynamic properties investigated. Introduction Of M8G into DNA sequences markedly stabilizes the Z conformation under low salt conditions. The hexamer d(CGC[M8G]CG)2 exhibits a CD spectrum characteristic of the Z conformation under physiological salt conditions. The NOE-restrained refinement unequivocally demonstrated that d(CGC[m8G]CG)2 adopts a Z structure with all guanines in the syn conformation. The refined NMR structure is very similar to the Z form crystal structure of d(CGCGCG)2, with a root mean square deviation of 0.6 between the two structures. The contribution of m8G to the stabilization of Z-DNA has been estimated from the mid-point NaCl concentrations for the B-Z transition of various m8G-containing oligomers. The presence of m8G in d(CGC[m8G]CG)2 stabilizes the Z conformation by at least deltaG = -0.8 kcal/mol relative to the unmodified hexamer. The Z conformation was further stabilized by increasing the number of m8Gs incorporated and destabilized by incorporating syn-A or syn-T, found respectively in the (A,T)-containing alternating and non-alternating pyrimidine-purine sequences. The results suggest that the chemically less reactive m8G base is a useful agent for studying molecular interactions of Z-DNA or other DNA structures that incorporate syn-G conformation.

About this Structure

1TNE is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Synthesis, structure and thermodynamic properties of 8-methylguanine-containing oligonucleotides: Z-DNA under physiological salt conditions., Sugiyama H, Kawai K, Matsunaga A, Fujimoto K, Saito I, Robinson H, Wang AH, Nucleic Acids Res. 1996 Apr 1;24(7):1272-8. PMID:8614630

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