1s88

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(New page: 200px<br /><applet load="1s88" size="450" color="white" frame="true" align="right" spinBox="true" caption="1s88" /> '''NMR structure of a DNA duplex with two INA n...)
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[[Image:1s88.gif|left|200px]]<br /><applet load="1s88" size="350" color="white" frame="true" align="right" spinBox="true"
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'''NMR structure of a DNA duplex with two INA nucleotides inserted opposite each other, dCTCAACXCAAGCT:dAGCTTGXGTTGAG'''<br />
'''NMR structure of a DNA duplex with two INA nucleotides inserted opposite each other, dCTCAACXCAAGCT:dAGCTTGXGTTGAG'''<br />
==Overview==
==Overview==
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The intercalating nucleic acid (INA) presented in this paper is a novel, 1-O-(1-pyrenylmethyl)glycerol DNA intercalator that induces high thermal, affinity for complementary DNA. The duplex examined contained two INA, intercalators, denoted X, inserted directly opposite each other:, d(C(1)T(2)C(3)A(4)A(5)C(6)X(7)C(8)A(9)A(10)G(11)C(12)T(13)):d(A(14)G(15)C(, 16)T(17)-T(18)G(19)X(20)G(21)T(22)T(23)G(24)A(25)G(26)). Unlike most other, nucleotide analogues, DNA with INA inserted has a lower affinity for, hybridizing to complementary DNA with an INA inserted directly opposite, than to complementary unmodified DNA. In this study we used, two-dimensional (1)H NMR spectroscopy to determine a high-resolution, solution structure of the weak INA-INA duplex. A modified ISPA approach, was used to obtain interproton distance bounds from NOESY cross-peak, intensities. These distance bounds were used as restraints in molecular, dynamics (rMD) calculations. Twenty final structures were generated for, the duplex from a B-type DNA starting structure. The root-mean-square, deviation (RMSD) of the coordinates for the 20 structures of the complex, was 1.95 A. This rather large value, together with broad lines in the area, of insertion, reflect the high degree of internal motion in the complex., The determination of the structure revealed that both intercalators were, situated in the center of the helix, stacking with each other and the, neighboring nucleobases. The intercalation of the INAs caused an unwinding, of the helix in the insertion area, creating a ladderlike structure. The, structural changes observed upon intercalation were mainly of local, character; however, a broadening of the minor groove was found throughout, the helix.
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The intercalating nucleic acid (INA) presented in this paper is a novel 1-O-(1-pyrenylmethyl)glycerol DNA intercalator that induces high thermal affinity for complementary DNA. The duplex examined contained two INA intercalators, denoted X, inserted directly opposite each other: d(C(1)T(2)C(3)A(4)A(5)C(6)X(7)C(8)A(9)A(10)G(11)C(12)T(13)):d(A(14)G(15)C( 16)T(17)-T(18)G(19)X(20)G(21)T(22)T(23)G(24)A(25)G(26)). Unlike most other nucleotide analogues, DNA with INA inserted has a lower affinity for hybridizing to complementary DNA with an INA inserted directly opposite than to complementary unmodified DNA. In this study we used two-dimensional (1)H NMR spectroscopy to determine a high-resolution solution structure of the weak INA-INA duplex. A modified ISPA approach was used to obtain interproton distance bounds from NOESY cross-peak intensities. These distance bounds were used as restraints in molecular dynamics (rMD) calculations. Twenty final structures were generated for the duplex from a B-type DNA starting structure. The root-mean-square deviation (RMSD) of the coordinates for the 20 structures of the complex was 1.95 A. This rather large value, together with broad lines in the area of insertion, reflect the high degree of internal motion in the complex. The determination of the structure revealed that both intercalators were situated in the center of the helix, stacking with each other and the neighboring nucleobases. The intercalation of the INAs caused an unwinding of the helix in the insertion area, creating a ladderlike structure. The structural changes observed upon intercalation were mainly of local character; however, a broadening of the minor groove was found throughout the helix.
==About this Structure==
==About this Structure==
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1S88 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=1S88 OCA].
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1S88 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=1S88 OCA].
==Reference==
==Reference==
NMR structure determination of a modified DNA oligonucleotide containing a new intercalating nucleic acid., Nielsen CB, Petersen M, Pedersen EB, Hansen PE, Christensen UB, Bioconjug Chem. 2004 Mar-Apr;15(2):260-9. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15025521 15025521]
NMR structure determination of a modified DNA oligonucleotide containing a new intercalating nucleic acid., Nielsen CB, Petersen M, Pedersen EB, Hansen PE, Christensen UB, Bioconjug Chem. 2004 Mar-Apr;15(2):260-9. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15025521 15025521]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Christensen, U.B.]]
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[[Category: Christensen, U B.]]
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[[Category: Hansen, P.E.]]
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[[Category: Hansen, P E.]]
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[[Category: Nielsen, C.B.]]
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[[Category: Nielsen, C B.]]
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[[Category: Pedersen, E.B.]]
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[[Category: Pedersen, E B.]]
[[Category: Petersen, M.]]
[[Category: Petersen, M.]]
[[Category: dna]]
[[Category: dna]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 00:04:33 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:58:58 2008''

Revision as of 12:59, 21 February 2008


1s88

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NMR structure of a DNA duplex with two INA nucleotides inserted opposite each other, dCTCAACXCAAGCT:dAGCTTGXGTTGAG

Overview

The intercalating nucleic acid (INA) presented in this paper is a novel 1-O-(1-pyrenylmethyl)glycerol DNA intercalator that induces high thermal affinity for complementary DNA. The duplex examined contained two INA intercalators, denoted X, inserted directly opposite each other: d(C(1)T(2)C(3)A(4)A(5)C(6)X(7)C(8)A(9)A(10)G(11)C(12)T(13)):d(A(14)G(15)C( 16)T(17)-T(18)G(19)X(20)G(21)T(22)T(23)G(24)A(25)G(26)). Unlike most other nucleotide analogues, DNA with INA inserted has a lower affinity for hybridizing to complementary DNA with an INA inserted directly opposite than to complementary unmodified DNA. In this study we used two-dimensional (1)H NMR spectroscopy to determine a high-resolution solution structure of the weak INA-INA duplex. A modified ISPA approach was used to obtain interproton distance bounds from NOESY cross-peak intensities. These distance bounds were used as restraints in molecular dynamics (rMD) calculations. Twenty final structures were generated for the duplex from a B-type DNA starting structure. The root-mean-square deviation (RMSD) of the coordinates for the 20 structures of the complex was 1.95 A. This rather large value, together with broad lines in the area of insertion, reflect the high degree of internal motion in the complex. The determination of the structure revealed that both intercalators were situated in the center of the helix, stacking with each other and the neighboring nucleobases. The intercalation of the INAs caused an unwinding of the helix in the insertion area, creating a ladderlike structure. The structural changes observed upon intercalation were mainly of local character; however, a broadening of the minor groove was found throughout the helix.

About this Structure

1S88 is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

NMR structure determination of a modified DNA oligonucleotide containing a new intercalating nucleic acid., Nielsen CB, Petersen M, Pedersen EB, Hansen PE, Christensen UB, Bioconjug Chem. 2004 Mar-Apr;15(2):260-9. PMID:15025521

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