1y8d

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(New page: 200px<br /> <applet load="1y8d" size="450" color="white" frame="true" align="right" spinBox="true" caption="1y8d" /> '''Dimeric parallel-stranded tetraplex with 3+...)
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'''Dimeric parallel-stranded tetraplex with 3+1 5' G-tetrad interface, single-residue chain reversal loops and GAG triad in the context of A(GGGG) pentad'''<br />
'''Dimeric parallel-stranded tetraplex with 3+1 5' G-tetrad interface, single-residue chain reversal loops and GAG triad in the context of A(GGGG) pentad'''<br />
==Overview==
==Overview==
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We report on the NMR-based solution structure of the 93del, d(GGGGTGGGAGGAGGGT) aptamer, a potent nanomolar inhibitor of HIV-1, integrase. This guanine-rich DNA sequence adopts an unusually stable, dimeric quadruplex architecture in K+ solution. Within each 16-nt monomer, subunit, which contains one A.(G.G.G.G) pentad sandwiched between two, G.G.G.G tetrads, all G-stretches are parallel, and all guanines are anti, with the exception of G1, which is syn. Dimer formation is achieved, through mutual pairing of G1 of one monomer, with G2, G6, and G13 of the, other monomer, to complete G.G.G.G tetrad formation. There are three, single-nucleotide double-chain-reversal loops within each monomer fold, such that the first (T5) and third (A12) loops bridge three G-tetrad, layers, whereas the second (A9) loop bridges two G-tetrad layers and, participates in A.(G.G.G.G) pentad formation. Results of NMR and of, integrase inhibition assays on loop-modified sequences allowed us to, propose a strategy toward the potential design of improved HIV-1 integrase, inhibitors. Finally, we propose a model, based on molecular docking, approaches, for positioning the 93del dimeric DNA quadruplex within a, basic channel/canyon formed between subunits of a dimer of dimers of HIV-1, integrase.
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We report on the NMR-based solution structure of the 93del d(GGGGTGGGAGGAGGGT) aptamer, a potent nanomolar inhibitor of HIV-1 integrase. This guanine-rich DNA sequence adopts an unusually stable dimeric quadruplex architecture in K+ solution. Within each 16-nt monomer subunit, which contains one A.(G.G.G.G) pentad sandwiched between two G.G.G.G tetrads, all G-stretches are parallel, and all guanines are anti with the exception of G1, which is syn. Dimer formation is achieved through mutual pairing of G1 of one monomer, with G2, G6, and G13 of the other monomer, to complete G.G.G.G tetrad formation. There are three single-nucleotide double-chain-reversal loops within each monomer fold, such that the first (T5) and third (A12) loops bridge three G-tetrad layers, whereas the second (A9) loop bridges two G-tetrad layers and participates in A.(G.G.G.G) pentad formation. Results of NMR and of integrase inhibition assays on loop-modified sequences allowed us to propose a strategy toward the potential design of improved HIV-1 integrase inhibitors. Finally, we propose a model, based on molecular docking approaches, for positioning the 93del dimeric DNA quadruplex within a basic channel/canyon formed between subunits of a dimer of dimers of HIV-1 integrase.
==About this Structure==
==About this Structure==
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1Y8D 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=1Y8D OCA].
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1Y8D 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=1Y8D OCA].
==Reference==
==Reference==
An interlocked dimeric parallel-stranded DNA quadruplex: a potent inhibitor of HIV-1 integrase., Phan AT, Kuryavyi V, Ma JB, Faure A, Andreola ML, Patel DJ, Proc Natl Acad Sci U S A. 2005 Jan 18;102(3):634-9. Epub 2005 Jan 6. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15637158 15637158]
An interlocked dimeric parallel-stranded DNA quadruplex: a potent inhibitor of HIV-1 integrase., Phan AT, Kuryavyi V, Ma JB, Faure A, Andreola ML, Patel DJ, Proc Natl Acad Sci U S A. 2005 Jan 18;102(3):634-9. Epub 2005 Jan 6. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15637158 15637158]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Andreola, M.L.]]
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[[Category: Andreola, M L.]]
[[Category: Faure, A.]]
[[Category: Faure, A.]]
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[[Category: Kuryavyi, V.V.]]
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[[Category: Kuryavyi, V V.]]
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[[Category: Ma, J.B.]]
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[[Category: Ma, J B.]]
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[[Category: Patel, D.J.]]
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[[Category: Patel, D J.]]
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[[Category: Phan, A.T.]]
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[[Category: Phan, A T.]]
[[Category: dimeric parallel-stranded quadruplex; dna aptamer;hiv-1 integrase inhibitor design; 3+1 g-tetrad; single nucleotide chain reversal loop; gag triad; (a)gggg pentad]]
[[Category: dimeric parallel-stranded quadruplex; dna aptamer;hiv-1 integrase inhibitor design; 3+1 g-tetrad; single nucleotide chain reversal loop; gag triad; (a)gggg pentad]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Thu Nov 8 14:36:30 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:02:46 2008''

Revision as of 14:02, 21 February 2008


1y8d

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Dimeric parallel-stranded tetraplex with 3+1 5' G-tetrad interface, single-residue chain reversal loops and GAG triad in the context of A(GGGG) pentad

Overview

We report on the NMR-based solution structure of the 93del d(GGGGTGGGAGGAGGGT) aptamer, a potent nanomolar inhibitor of HIV-1 integrase. This guanine-rich DNA sequence adopts an unusually stable dimeric quadruplex architecture in K+ solution. Within each 16-nt monomer subunit, which contains one A.(G.G.G.G) pentad sandwiched between two G.G.G.G tetrads, all G-stretches are parallel, and all guanines are anti with the exception of G1, which is syn. Dimer formation is achieved through mutual pairing of G1 of one monomer, with G2, G6, and G13 of the other monomer, to complete G.G.G.G tetrad formation. There are three single-nucleotide double-chain-reversal loops within each monomer fold, such that the first (T5) and third (A12) loops bridge three G-tetrad layers, whereas the second (A9) loop bridges two G-tetrad layers and participates in A.(G.G.G.G) pentad formation. Results of NMR and of integrase inhibition assays on loop-modified sequences allowed us to propose a strategy toward the potential design of improved HIV-1 integrase inhibitors. Finally, we propose a model, based on molecular docking approaches, for positioning the 93del dimeric DNA quadruplex within a basic channel/canyon formed between subunits of a dimer of dimers of HIV-1 integrase.

About this Structure

1Y8D is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

An interlocked dimeric parallel-stranded DNA quadruplex: a potent inhibitor of HIV-1 integrase., Phan AT, Kuryavyi V, Ma JB, Faure A, Andreola ML, Patel DJ, Proc Natl Acad Sci U S A. 2005 Jan 18;102(3):634-9. Epub 2005 Jan 6. PMID:15637158

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