1b0s

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(New page: 200px<br /><applet load="1b0s" size="450" color="white" frame="true" align="right" spinBox="true" caption="1b0s" /> '''BINDING OF AR-1-144, A TRI-IMIDAZOLE DNA MIN...)
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'''BINDING OF AR-1-144, A TRI-IMIDAZOLE DNA MINOR GROOVE BINDER, TO CCGG SEQUENCE ANALYZED BY NMR SPECTROSCOPY'''<br />
'''BINDING OF AR-1-144, A TRI-IMIDAZOLE DNA MINOR GROOVE BINDER, TO CCGG SEQUENCE ANALYZED BY NMR SPECTROSCOPY'''<br />
==Overview==
==Overview==
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The interactions of, N-[2-(dimethylamino)ethyl]-1-methyl-4-[1-methyl-4-[4-formamido-1-meth, ylimidazole-2-carboxamido]imidazole-2-carboxamido]imidazole-2-c arboxa, mide (AR-1-144), a tri-imidazole polyamide minor groove binder, with DNA, have been investigated by NMR and CD spectroscopy. A series of DNA, oligonucleotides with a C/G-containing four-bp core, i.e. CCGG, CGCG, GGCC, and GCGC, have been titrated with AR-1-144 at different ratios., AR-1-144 favors the CCGG sequence. The flanking sequence of the CCGG core, also influences the binding preference, with a C or T being favored on the, 3'-side of the CCGG core. The three-dimensional structure of the symmetric, 2:1 side-by-side complex of AR-1-144 and GAACCGGTTC, determined by, NOE-constrained NMR refinement, reveals that each AR-1-144 binds to four, base pairs, i.e. at C5-G6-G7-T8, with every amide-imidazole unit forming, two potential hydrogen bonds with DNA. The same DNA binding preference of, AR-1-144 was also confirmed by circular dichroism spectroscopy, indicating, that the DNA binding preference of AR-1-144 is independent of, concentration. The cooperative binding of an AR-1-144 homodimer to the, (purine)CCGG(pyrimidine) core sequence appears to be weaker than that of, the distamycin A homodimer to A/T sequences, most likely due to the, diminished hydrophobic interactions between AR-1-144 and DNA. Our results, are consistent with previous footprinting data and explain the binding, pattern found in the crystal structure of a di-imidazole drug bound to, CATGGCCATG.
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The interactions of N-[2-(dimethylamino)ethyl]-1-methyl-4-[1-methyl-4-[4-formamido-1-meth ylimidazole-2-carboxamido]imidazole-2-carboxamido]imidazole-2-c arboxa mide (AR-1-144), a tri-imidazole polyamide minor groove binder, with DNA have been investigated by NMR and CD spectroscopy. A series of DNA oligonucleotides with a C/G-containing four-bp core, i.e. CCGG, CGCG, GGCC, and GCGC, have been titrated with AR-1-144 at different ratios. AR-1-144 favors the CCGG sequence. The flanking sequence of the CCGG core also influences the binding preference, with a C or T being favored on the 3'-side of the CCGG core. The three-dimensional structure of the symmetric 2:1 side-by-side complex of AR-1-144 and GAACCGGTTC, determined by NOE-constrained NMR refinement, reveals that each AR-1-144 binds to four base pairs, i.e. at C5-G6-G7-T8, with every amide-imidazole unit forming two potential hydrogen bonds with DNA. The same DNA binding preference of AR-1-144 was also confirmed by circular dichroism spectroscopy, indicating that the DNA binding preference of AR-1-144 is independent of concentration. The cooperative binding of an AR-1-144 homodimer to the (purine)CCGG(pyrimidine) core sequence appears to be weaker than that of the distamycin A homodimer to A/T sequences, most likely due to the diminished hydrophobic interactions between AR-1-144 and DNA. Our results are consistent with previous footprinting data and explain the binding pattern found in the crystal structure of a di-imidazole drug bound to CATGGCCATG.
==About this Structure==
==About this Structure==
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1B0S is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with AR1 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1B0S OCA].
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1B0S is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=AR1:'>AR1</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1B0S OCA].
==Reference==
==Reference==
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[[Category: Kaenzig, C.]]
[[Category: Kaenzig, C.]]
[[Category: Lee, M.]]
[[Category: Lee, M.]]
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[[Category: Wang, A.H.J.]]
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[[Category: Wang, A H.J.]]
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[[Category: Yang, X.L.]]
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[[Category: Yang, X L.]]
[[Category: AR1]]
[[Category: AR1]]
[[Category: anticancer drug]]
[[Category: anticancer drug]]
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[[Category: sequence specific recognition]]
[[Category: sequence specific recognition]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sat Nov 24 23:35:11 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:50:17 2008''

Revision as of 09:50, 21 February 2008


1b0s

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BINDING OF AR-1-144, A TRI-IMIDAZOLE DNA MINOR GROOVE BINDER, TO CCGG SEQUENCE ANALYZED BY NMR SPECTROSCOPY

Overview

The interactions of N-[2-(dimethylamino)ethyl]-1-methyl-4-[1-methyl-4-[4-formamido-1-meth ylimidazole-2-carboxamido]imidazole-2-carboxamido]imidazole-2-c arboxa mide (AR-1-144), a tri-imidazole polyamide minor groove binder, with DNA have been investigated by NMR and CD spectroscopy. A series of DNA oligonucleotides with a C/G-containing four-bp core, i.e. CCGG, CGCG, GGCC, and GCGC, have been titrated with AR-1-144 at different ratios. AR-1-144 favors the CCGG sequence. The flanking sequence of the CCGG core also influences the binding preference, with a C or T being favored on the 3'-side of the CCGG core. The three-dimensional structure of the symmetric 2:1 side-by-side complex of AR-1-144 and GAACCGGTTC, determined by NOE-constrained NMR refinement, reveals that each AR-1-144 binds to four base pairs, i.e. at C5-G6-G7-T8, with every amide-imidazole unit forming two potential hydrogen bonds with DNA. The same DNA binding preference of AR-1-144 was also confirmed by circular dichroism spectroscopy, indicating that the DNA binding preference of AR-1-144 is independent of concentration. The cooperative binding of an AR-1-144 homodimer to the (purine)CCGG(pyrimidine) core sequence appears to be weaker than that of the distamycin A homodimer to A/T sequences, most likely due to the diminished hydrophobic interactions between AR-1-144 and DNA. Our results are consistent with previous footprinting data and explain the binding pattern found in the crystal structure of a di-imidazole drug bound to CATGGCCATG.

About this Structure

1B0S is a Protein complex structure of sequences from [1] with as ligand. Full crystallographic information is available from OCA.

Reference

Binding of AR-1-144, a tri-imidazole DNA minor groove binder, to CCGG sequence analyzed by NMR spectroscopy., Yang XL, Kaenzig C, Lee M, Wang AH, Eur J Biochem. 1999 Aug;263(3):646-55. PMID:10469127

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