8WU5

The complex of CAG repeat sequence-specific binding cPIP and dsDNA with A-A mismatch

これはPDB形式変換不可エントリーです。

8WU5 の概要

• エントリーDOI: 10.2210/pdb8wu5/pdb
• 分子名称: DNA (5'-D(*GP*CP*(CBR)P*GP*AP*GP*CP*AP*GP*CP*AP*CP*GP*GP*C)-3'), (1^2Z,4^2Z,11^2Z,14^2Z,22^2Z,25^2Z,32^2Z,35^2Z,19R,40R)-1^1,4^1,11^1,14^1,22^1,25^1,32^1,35^1-octamethyl-2,5,9,12,15,20,23,26,30,33,36,41-dodecaoxo-1^1H,4^1H,11^1H,14^1H,22^1H,25^1H,32^1H,35^1H-3,6,10,13,16,21,24,27,31,34,37,42-dodecaaza-1(2,4),11,22,32(4,2)-tetraimidazola-4,14,25,35(4,2)-tetrapyrrolacyclodotetracontaphane-19,40-diaminium (2 entities in total)
• 機能のキーワード: dna minor groove binder pyrrole imidazole polyamide a-a mismatch dna cag repeat, dna
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 21382.22

構造登録者

Abe, K.,Takeda, K.,Sugiyama, H. (登録日: 2023-10-20, 公開日: 2024-06-05, 最終更新日: 2024-06-12)

主引用文献

Abe, K.,Hirose, Y.,Kumagai, T.,Hashiya, K.,Hidaka, K.,Emura, T.,Bando, T.,Takeda, K.,Sugiyama, H.
Structural Studies of a Complex of a CAG/CTG Repeat Sequence-Specific Binding Molecule and A-A-Mismatch-Containing DNA.
Jacs Au, 4:1801-1810, 2024

PubMed Abstract: Triplet repeat diseases are caused by the abnormal elongation of repeated sequences comprising three bases. In particular, the elongation of CAG/CTG repeat sequences is thought to result in conditions such as Huntington's disease and myotonic dystrophy type 1. Although the causes of these diseases are known, fundamental treatments have not been established, and specific drugs are expected to be developed. Pyrrole imidazole polyamide (PIP) is a class of molecules that binds to the minor groove of the DNA duplex in a sequence-specific manner; because of this property, it shows promise in drug discovery applications. Earlier, it was reported that PIP designed to bind CAG/CTG repeat sequences suppresses the genes that cause triplet repeat diseases. In this study, we performed an X-ray crystal structure analysis of a complex of double-stranded DNA containing A-A mismatched base pairs and a cyclic-PIP that binds specifically to CAG/CTG sequences. Furthermore, the validity and characteristics of this structure were analyzed using molecular modeling, energy calculations, gel electrophoresis, and surface plasmon resonance. With our direct observation using atomic force microscopy and DNA origami, we revealed that the PIP caused structural changes in the DNA strands carrying the expanded CAG/CTG repeat. Overall, our study provides new insight into PIP from a structural perspective.

PubMed: 38818057
DOI: 10.1021/jacsau.3c00830

実験手法

X-RAY DIFFRACTION (2.8 Å)