Free energy landscape and transition pathways from Watson-Crick to Hoogsteen base pairing in free duplex DNA

被引:34
|
作者
Yang, Changwon [1 ,2 ]
Kim, Eunae [3 ]
Pak, Youngshang [1 ,2 ]
机构
[1] Pusan Natl Univ, Dept Chem, Busan 609735, South Korea
[2] Pusan Natl Univ, Inst Funct Mat, Busan 609735, South Korea
[3] Chosun Univ, Coll Pharm, Kwangju 501759, South Korea
基金
新加坡国家研究基金会;
关键词
NUCLEIC-ACID STRUCTURES; IMINO PROTON-EXCHANGE; PARTICLE MESH EWALD; MOLECULAR-DYNAMICS; REVERSE HOOGSTEEN; FORCE-FIELD; B-DNA; SIMULATIONS; VISUALIZATION; SYSTEM;
D O I
10.1093/nar/gkv796
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Houghton (HG) base pairing plays a central role in the DNA binding of proteins and small ligands. Probing detailed transition mechanism from Watson-Crick (WC) to HG base pair (bp) formation in duplex DNAs is of fundamental importance in terms of revealing intrinsic functions of double helical DNAs beyond their sequence determined functions. We investigated a free energy landscape of a free B-DNA with an adenosine-thymine (A-T) rich sequence to probe its conformational transition pathways from WC to HG base pairing. The free energy landscape was computed with a state-of-art two-dimensional umbrella molecular dynamics simulation at the all-atom level. The present simulation showed that in an isolated duplex DNA, the spontaneous transition from WC to HG bp takes place via multiple pathways. Notably, base flipping into the major and minor grooves was found to play an important role in forming these multiple transition pathways. This finding suggests that naked B-DNA under normal conditions has an inherent ability to form HG bps via spontaneous base opening events.
引用
收藏
页码:7769 / 7778
页数:10
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