哑铃
DNA连接酶
DNA
结扎
碱基对
化学
循环(图论)
计算生物学
生物物理学
物理
生物
生物化学
数学
分子生物学
组合数学
生理学
作者
Alberto Mills,Federico Gago
出处
期刊:Molecules
[MDPI AG]
日期:2021-05-19
卷期号:26 (10): 3017-3017
被引量:2
标识
DOI:10.3390/molecules26103017
摘要
The experimental construction of a double-stranded DNA microcircle of only 42 base pairs entailed a great deal of ingenuity and hard work. However, figuring out the three-dimensional structures of intermediates and the final product can be particularly baffling. Using a combination of model building and unrestrained molecular dynamics simulations in explicit solvent we have characterized the different DNA structures involved along the process. Our 3D models of the single-stranded DNA molecules provide atomic insight into the recognition event that must take place for the DNA bases in the cohesive tail of the hairpin to pair with their complementary bases in the single-stranded loops of the dumbbell. We propose that a kissing loop involving six base pairs makes up the core of the nascent dsDNA microcircle. We also suggest a feasible pathway for the hybridization of the remaining complementary bases and characterize the final covalently closed dsDNA microcircle as possessing two well-defined U-turns. Additional models of the pre-ligation complex of T4 DNA ligase with the DNA dumbbell and the post-ligation pre-release complex involving the same enzyme and the covalently closed DNA microcircle are shown to be compatible with enzyme recognition and gap ligation.
科研通智能强力驱动
Strongly Powered by AbleSci AI