Literature DB >> 12079378

Crystal structure of the potassium form of an Oxytricha nova G-quadruplex.

Shozeb Haider1, Gary N Parkinson, Stephen Neidle.   

Abstract

The crystal structures of the potassium-containing quadruplex formed from the Oxytricha nova sequence d(GGGGTTTTGGGG) are reported, in two space groups, the orthorhombic P2(1)2(1)2(1) and the trigonal P3(2)21, which diffract to 2.0 A and 1.49 A, respectively. The orthorhombic form contains two independent quadruplexes in the asymmetric unit, and the trigonal form contains one. All three of these quadruplexes adopt an identical fold, with two strands forming an antiparallel diagonal arrangement. This is identical with that observed previously in NMR studies of the native sodium and potassium forms, and a crystallographic analysis of it complexed with an O. nova protein. The present analysis demonstrates that the native structure is the same in solution and in the crystalline state and, moreover, that the nature of the counter-ion does not affect the overall fold of this quadruplex. The analysis corrects an earlier crystallographic study of this quadruplex. The conformation of the tetra-thymine loop is described in detail, which involves the third thymine base folding back to interact with the first thymine base. The water networks in the grooves and loops are described and, in particular, the ability of water molecules to form a continuous spine of hydration in the narrow groove is detailed. Each quadruplex has five potassium ions organised in a linear channel, with square antiprismatic coordination to each ion from oxygen atoms.

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Year:  2002        PMID: 12079378     DOI: 10.1016/S0022-2836(02)00428-X

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  100 in total

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6.  Binding linkage in a telomere DNA-protein complex at the ends of Oxytricha nova chromosomes.

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Journal:  J Mol Biol       Date:  2005-07-29       Impact factor: 5.469

7.  Thermodynamic characterization of binding Oxytricha nova single strand telomere DNA with the alpha protein N-terminal domain.

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Journal:  J Mol Biol       Date:  2006-04-25       Impact factor: 5.469

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10.  Molecular dynamics simulations of Guanine quadruplex loops: advances and force field limitations.

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Journal:  Biophys J       Date:  2004-07       Impact factor: 4.033

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