1cx5

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(New page: 200px<br /><applet load="1cx5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cx5" /> '''ANTISENSE DNA/RNA HYBRID CONTAINING MODIFIED...)
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'''ANTISENSE DNA/RNA HYBRID CONTAINING MODIFIED BACKBONE'''<br />
'''ANTISENSE DNA/RNA HYBRID CONTAINING MODIFIED BACKBONE'''<br />
==Overview==
==Overview==
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The solution structure of an antisense DNA.RNA hybrid duplex, d(CGCGTT-MMI-TTGCGC).r(GCGCAAAACGCG) (designated R4), containing an MMI, backbone linker [3'-CH(2)N(CH(3))-O5'], is elucidated. The structural, details of the MMI linker, its structural effects on the neighboring, residues, and the molecular basis of the MMI effects are examined. The, lipophilic N-methyl group of MMI is peripheral to the helix, assuming a, conformation that is most stable with regard to the N-O torsion angle. The, MMI linker promotes a 3'-endo conformation for the sugar moieties at both, 3'- and 5'-adjacent positions and a backbone kink involving distant, residues along the 3'-direction. Comparison of R4 with other analogous, hybrid duplexes previously studied in this laboratory reveals a new family, of low-energy helical conformations that can be accommodated in stable, duplexes and a common feature of C3'-modified sugars for adopting a, C3'-endo pucker. The results of these studies emphasize the interplay of, several factors that govern the formation of stable hybrid duplexes and, provide a basis for the understanding of the biological role of the MMI, modifications, which are important building blocks for a family of, promising chimeric antisense oligonucleotides.
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The solution structure of an antisense DNA.RNA hybrid duplex, d(CGCGTT-MMI-TTGCGC).r(GCGCAAAACGCG) (designated R4), containing an MMI backbone linker [3'-CH(2)N(CH(3))-O5'], is elucidated. The structural details of the MMI linker, its structural effects on the neighboring residues, and the molecular basis of the MMI effects are examined. The lipophilic N-methyl group of MMI is peripheral to the helix, assuming a conformation that is most stable with regard to the N-O torsion angle. The MMI linker promotes a 3'-endo conformation for the sugar moieties at both 3'- and 5'-adjacent positions and a backbone kink involving distant residues along the 3'-direction. Comparison of R4 with other analogous hybrid duplexes previously studied in this laboratory reveals a new family of low-energy helical conformations that can be accommodated in stable duplexes and a common feature of C3'-modified sugars for adopting a C3'-endo pucker. The results of these studies emphasize the interplay of several factors that govern the formation of stable hybrid duplexes and provide a basis for the understanding of the biological role of the MMI modifications, which are important building blocks for a family of promising chimeric antisense oligonucleotides.
==About this Structure==
==About this Structure==
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1CX5 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=1CX5 OCA].
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1CX5 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=1CX5 OCA].
==Reference==
==Reference==
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[[Category: nmr]]
[[Category: nmr]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:03:59 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:10:39 2008''

Revision as of 10:10, 21 February 2008


1cx5

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ANTISENSE DNA/RNA HYBRID CONTAINING MODIFIED BACKBONE

Overview

The solution structure of an antisense DNA.RNA hybrid duplex, d(CGCGTT-MMI-TTGCGC).r(GCGCAAAACGCG) (designated R4), containing an MMI backbone linker [3'-CH(2)N(CH(3))-O5'], is elucidated. The structural details of the MMI linker, its structural effects on the neighboring residues, and the molecular basis of the MMI effects are examined. The lipophilic N-methyl group of MMI is peripheral to the helix, assuming a conformation that is most stable with regard to the N-O torsion angle. The MMI linker promotes a 3'-endo conformation for the sugar moieties at both 3'- and 5'-adjacent positions and a backbone kink involving distant residues along the 3'-direction. Comparison of R4 with other analogous hybrid duplexes previously studied in this laboratory reveals a new family of low-energy helical conformations that can be accommodated in stable duplexes and a common feature of C3'-modified sugars for adopting a C3'-endo pucker. The results of these studies emphasize the interplay of several factors that govern the formation of stable hybrid duplexes and provide a basis for the understanding of the biological role of the MMI modifications, which are important building blocks for a family of promising chimeric antisense oligonucleotides.

About this Structure

1CX5 is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

NMR structure of an antisense DNA.RNA hybrid duplex containing a 3'-CH(2)N(CH(3))-O-5' or an MMI backbone linker., Yang X, Han X, Cross C, Bare S, Sanghvi Y, Gao X, Biochemistry. 1999 Sep 28;38(39):12586-96. PMID:10504227

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