PDBsum entry 2dpb

DNA

PDB id: 2dpb

Contents

DNA/RNA

Ligands

CMY ×2

Metals

__K

Waters ×236

PDB id:

2dpb

Name:

DNA

Title:

Crystal structure of d(cgcgaatxcgcg) where x is 5-(n-aminohexyl) carbamoyl-2'-deoxyuridine

Structure:

DNA (5'-d( Dcp Dgp Dcp Dgp Dap Dap Dtp Dup Dcp Dgp Dcp Dg)- 3'). Chain: a, b. Engineered: yes

Source:

Synthetic: yes. Other_details: this DNA dodecamer is a synthetic construct.

Resolution:

1.50Å R-factor: 0.193 R-free: 0.245

Authors:

E.C.M.Juan,J.Kondo,T.Kurihara,T.Ito,Y.Ueno,A.Matsuda,A.Takenaka

Key ref:

E.C.Juan et al. (2007). Crystal structures of DNA:DNA and DNA:RNA duplexes containing 5-(N-aminohexyl)carbamoyl-modified uracils reveal the basis for properties as antigene and antisense molecules. Nucleic Acids Res, 35, 1969-1977. PubMed id: 17341465

Date:

08-May-06 Release date: 17-Apr-07

DNA/RNA chains

C-G-C-G-A-A-T-U-C-G-C-G 12 bases

C-G-C-G-A-A-T-U-C-G-C-G 12 bases

Nucleic Acids Res 35:1969-1977 (2007)

PubMed id: 17341465

Crystal structures of DNA:DNA and DNA:RNA duplexes containing 5-(N-aminohexyl)carbamoyl-modified uracils reveal the basis for properties as antigene and antisense molecules.

E.C.Juan, J.Kondo, T.Kurihara, T.Ito, Y.Ueno, A.Matsuda, A.Takénaka.

ABSTRACT

Oligonucleotides containing 5-(N-aminohexyl)carbamoyl-modified uracils have promising features for applications as antigene and antisense therapies. Relative to unmodified DNA, oligonucleotides containing 5-(N-aminohexyl)carbamoyl-2'-deoxyuridine ((N)U) or 5-(N-aminohexyl)carbamoyl-2'-O-methyluridine ((N)U(m)), respectively exhibit increased binding affinity for DNA and RNA, and enhanced nuclease resistance. To understand the structural implications of (N)U and (N)U(m) substitutions, we have determined the X-ray crystal structures of DNA:DNA duplexes containing either (N)U or (N)U(m) and of DNA:RNA hybrid duplexes containing (N)U(m). The aminohexyl chains are fixed in the major groove through hydrogen bonds between the carbamoyl amino groups and the uracil O4 atoms. The terminal ammonium cations on these chains could interact with the phosphate oxygen anions of the residues in the target strands. These interactions partly account for the increased target binding affinity and nuclease resistance. In contrast to (N)U, (N)U(m) decreases DNA binding affinity. This could be explained by the drastic changes in sugar puckering and in the minor groove widths and hydration structures seen in the (N)U(m) containing DNA:DNA duplex structure. The conformation of (N)U(m), however, is compatible with the preferred conformation in DNA:RNA hybrid duplexes. Furthermore, the ability of (N)U(m) to render the duplexes with altered minor grooves may increase nuclease resistance and elicit RNase H activity.