College of Life Sciences, Guizhou University, Guiyang 550025, China.
Laboratory of Bioorganic chemistry, Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China.
Molecules. 2017 Jun 22;22(7):1011. doi: 10.3390/molecules22071011.
In the 15-mer catalytic core of 10-23 DNAzyme, each residue contributes to the catalytic conformation differently. Here, the critically conserved T4 and the least conserved T8 were modified on their 5-position with hydroxyl, imidazolyl, and amino groups with a hydrogen-bonding ability. These external functional groups induced new interactions within the catalytic core, resulting in both negative and positive effects on the catalytic activity of 10-23 DNAzyme, and the different linkages could be used to modulate the effect of the functional groups. The conservation of T4 and T8 could be recognized at the level of the nucleobase, but at the level of the functional group, T4 is not completely conserved. Their 5-methyl groups could be modified for a better performance in terms of the DNAzyme.
在 10-23 DNA 酶的 15 -mer 催化核心中,每个残基对催化构象的贡献都不同。在这里,高度保守的 T4 和最不保守的 T8 在其 5 位被修饰为具有氢键能力的羟基、咪唑基和氨基。这些外部功能基团在催化核心内诱导了新的相互作用,对 10-23 DNA 酶的催化活性产生了正反两方面的影响,并且不同的键合方式可以用来调节功能基团的作用。T4 和 T8 的保守性可以在核碱基水平上得到识别,但在功能基团水平上,T4 并不完全保守。它们的 5-甲基基团可以被修饰,以提高 DNA 酶的性能。