1mlx

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(New page: 200px<br /><applet load="1mlx" size="450" color="white" frame="true" align="right" spinBox="true" caption="1mlx, resolution 1.25&Aring;" /> '''Crystal Structure An...)
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[[Image:1mlx.gif|left|200px]]<br /><applet load="1mlx" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1mlx.gif|left|200px]]<br /><applet load="1mlx" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1mlx, resolution 1.25&Aring;" />
caption="1mlx, resolution 1.25&Aring;" />
'''Crystal Structure Analysis of a 2'-O-[2-(Methylthio)-ethyl]-Modified Oligodeoxynucleotide Duplex'''<br />
'''Crystal Structure Analysis of a 2'-O-[2-(Methylthio)-ethyl]-Modified Oligodeoxynucleotide Duplex'''<br />
==Overview==
==Overview==
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A novel 2'-modification, 2'-O-[2-(methylthio)ethyl] or 2'-O-MTE, has been, incorporated into oligonucleotides and evaluated for properties relevant, to antisense activity. The results were compared with the previously, characterized 2'-O-[2-(methoxy)ethyl] 2'-O-MOE modification. As expected, the 2'-O-MTE modified oligonucleotides exhibited improved binding to human, serum albumin compared to the 2'-O-MOE modified oligonucleotides. The, 2'-O-MTE oligonucleotides maintained high binding affinity to target RNA., Nuclease digestion of 2'-O-MTE oligonucleotides showed that they have, limited resistance to exonuclease degradation. We analyzed the crystal, structure of a decamer DNA duplex containing the 2'-O-MTE modifcation., Analysis of the crystal structure provides insight into the improved RNA, binding affinity, protein binding affinity and limited resistance of, 2'-O-MTE modified oligonucleotides to exonuclease degradation.
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A novel 2'-modification, 2'-O-[2-(methylthio)ethyl] or 2'-O-MTE, has been incorporated into oligonucleotides and evaluated for properties relevant to antisense activity. The results were compared with the previously characterized 2'-O-[2-(methoxy)ethyl] 2'-O-MOE modification. As expected, the 2'-O-MTE modified oligonucleotides exhibited improved binding to human serum albumin compared to the 2'-O-MOE modified oligonucleotides. The 2'-O-MTE oligonucleotides maintained high binding affinity to target RNA. Nuclease digestion of 2'-O-MTE oligonucleotides showed that they have limited resistance to exonuclease degradation. We analyzed the crystal structure of a decamer DNA duplex containing the 2'-O-MTE modifcation. Analysis of the crystal structure provides insight into the improved RNA binding affinity, protein binding affinity and limited resistance of 2'-O-MTE modified oligonucleotides to exonuclease degradation.
==About this Structure==
==About this Structure==
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1MLX 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=1MLX OCA].
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1MLX 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=1MLX OCA].
==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Egli, M.]]
[[Category: Egli, M.]]
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[[Category: Fraser, A.S.]]
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[[Category: Fraser, A S.]]
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[[Category: Kawasaki, A.M.]]
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[[Category: Kawasaki, A M.]]
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[[Category: Leeds, J.M.]]
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[[Category: Leeds, J M.]]
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[[Category: Lesnik, E.A.]]
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[[Category: Lesnik, E A.]]
[[Category: Manoharan, M.]]
[[Category: Manoharan, M.]]
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[[Category: Prakash, T.P.]]
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[[Category: Prakash, T P.]]
[[Category: Sioufi, N.]]
[[Category: Sioufi, N.]]
[[Category: Teplova, M.]]
[[Category: Teplova, M.]]
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[[Category: rna affinity]]
[[Category: rna affinity]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 04:19:40 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:56:31 2008''

Revision as of 11:56, 21 February 2008


1mlx, resolution 1.25Å

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Crystal Structure Analysis of a 2'-O-[2-(Methylthio)-ethyl]-Modified Oligodeoxynucleotide Duplex

Overview

A novel 2'-modification, 2'-O-[2-(methylthio)ethyl] or 2'-O-MTE, has been incorporated into oligonucleotides and evaluated for properties relevant to antisense activity. The results were compared with the previously characterized 2'-O-[2-(methoxy)ethyl] 2'-O-MOE modification. As expected, the 2'-O-MTE modified oligonucleotides exhibited improved binding to human serum albumin compared to the 2'-O-MOE modified oligonucleotides. The 2'-O-MTE oligonucleotides maintained high binding affinity to target RNA. Nuclease digestion of 2'-O-MTE oligonucleotides showed that they have limited resistance to exonuclease degradation. We analyzed the crystal structure of a decamer DNA duplex containing the 2'-O-MTE modifcation. Analysis of the crystal structure provides insight into the improved RNA binding affinity, protein binding affinity and limited resistance of 2'-O-MTE modified oligonucleotides to exonuclease degradation.

About this Structure

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

Reference

2'-O-[2-(methylthio)ethyl]-modified oligonucleotide: an analogue of 2'-O-[2-(methoxy)-ethyl]-modified oligonucleotide with improved protein binding properties and high binding affinity to target RNA., Prakash TP, Manoharan M, Kawasaki AM, Fraser AS, Lesnik EA, Sioufi N, Leeds JM, Teplova M, Egli M, Biochemistry. 2002 Oct 1;41(39):11642-8. PMID:12269806

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