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核苷酸补充剂如何增强 G-四链体/血红素系统过氧化物酶模拟 DNA 酶活性的研究进展。

Insights into how nucleotide supplements enhance the peroxidase-mimicking DNAzyme activity of the G-quadruplex/hemin system.

机构信息

Institut de Chimie Moléculaire, Université de Bourgogne (ICMUB), CNRS UMR6302, 9, avenue Alain Savary, 21000 Dijon, France.

出版信息

Nucleic Acids Res. 2012 Sep 1;40(17):8759-72. doi: 10.1093/nar/gks581. Epub 2012 Jun 22.

DOI:10.1093/nar/gks581
PMID:22730286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3458538/
Abstract

Since the initial discovery of the catalytic capability of short DNA fragments, this peculiar enzyme-like property (termed DNAzyme) has continued to garner much interest in the scientific community because of the virtually unlimited applications in developing new molecular devices. Alongside the exponential rise in the number of DNAzyme applications in the last past years, the search for convenient ways to improve its overall efficiency has only started to emerge. Credence has been lent to this strategy by the recent demonstration that the quadruplex-based DNAzyme proficiency can be enhanced by ATP supplements. Herein, we have made a further leap along this path, trying first of all to decipher the actual DNAzyme catalytic cycle (to gain insights into the steps ATP may influence), and subsequently investigating in detail the influence of all the parameters that govern the catalytic efficiency. We have extended this study to other nucleotides and quadruplexes, thus demonstrating the versatility and broad applicability of such an approach. The defined exquisitely efficient DNAzyme protocols were exploited to highlight the enticing advantages of this method via a 96-well plate experiment that enables the detection of nanomolar DNA concentrations in real-time with the naked-eye (see movie as Supplementary Data).

摘要

自从最初发现短 DNA 片段的催化能力以来,由于在开发新型分子器件方面具有几乎无限的应用潜力,这种特殊的酶样性质(称为 DNA 酶)一直引起科学界的极大兴趣。随着过去几年 DNA 酶应用数量的指数级增长,人们才开始寻求提高其整体效率的便捷方法。最近的一项研究表明,ATP 补充可以增强基于四链体的 DNA 酶的效能,这为这一策略提供了依据。在此,我们沿着这条道路更进一步,首先试图破解实际的 DNA 酶催化循环(深入了解 ATP 可能影响的步骤),然后详细研究控制催化效率的所有参数的影响。我们将这项研究扩展到其他核苷酸和四链体,从而证明了这种方法的多功能性和广泛适用性。通过 96 孔板实验利用定义的高效 DNA 酶方案来突出这种方法的诱人优势,该实验可以实时用肉眼检测纳摩尔级别的 DNA 浓度(请参见作为补充数据提供的电影)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/2ccd8e61a17c/gks581f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/b9b0d19572f7/gks581f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/d6ba28c0ea54/gks581f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/adf12c54b100/gks581f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/5a58b67a8ba8/gks581f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/10c6d58d1a9e/gks581f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/109892a3d7d7/gks581f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/0c032afd038d/gks581f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/2ccd8e61a17c/gks581f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/b9b0d19572f7/gks581f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/d6ba28c0ea54/gks581f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/adf12c54b100/gks581f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/5a58b67a8ba8/gks581f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/10c6d58d1a9e/gks581f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/109892a3d7d7/gks581f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/0c032afd038d/gks581f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef5/3458538/2ccd8e61a17c/gks581f8.jpg

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