Institute of Medical Science and Technology, National Sun Yat-sen University, No. 70, Lien-hai Road, Kaohsiung, 804201, Taiwan.
Department of Chemistry, National Sun Yat-sen University, No. 70, Lien-hai Road, Kaohsiung, 804201, Taiwan.
Nucleic Acids Res. 2024 Nov 11;52(20):e97. doi: 10.1093/nar/gkae822.
Here, we employed a fluorescence-based single molecule method called nuclease-induced stepwise photodropping (NISP) to measure in real time the DNA degradation mediated by mitochondrial genome maintenance exonuclease 1 (MGME1), a bidirectional single-stranded DNA (ssDNA)-specific exonuclease. The method detects a stepwise decrease in fluorescence signals from Cy3 fluorophores labeled on an immobilized DNA substrate. Using NISP, we successfully determined the DNA degradation rates of 6.3 ± 0.4 and 2.0 ± 0.1 nucleotides (nt) s-1 for MGME1 in the 5'-to-3' and 3'-to-5' directions, respectively. These results provide direct evidence of the stronger 5' directionality of MGME1, consistent with its established role in mitochondrial DNA maintenance. Importantly, when we employed NISP to investigate mung bean nuclease, an ss-specific endonuclease, we observed a markedly different NISP pattern, suggesting a distributive cleavage activity of the enzyme. Furthermore, we applied NISP to determine the ssDNA degradation behavior of the double-stranded-specific exonuclease, λ exonuclease. These findings underscore the capability of NISP to accurately and reliably measure the degradation of ssDNA by both exo- and endonucleases. Here, we demonstrate NISP as a powerful tool for investigating the ssDNA degradation behavior of nucleases at the single-molecule level.
在这里,我们采用了一种基于荧光的单分子方法,称为核酸酶诱导分步光滴(NISP),实时测量线粒体基因组维持外切酶 1(MGME1)介导的 DNA 降解,MGME1 是一种双向单链 DNA(ssDNA)特异性外切酶。该方法检测到标记在固定化 DNA 底物上的 Cy3 荧光团的荧光信号逐步下降。使用 NISP,我们成功确定了 MGME1 在 5'-3'和 3'-5'方向的 DNA 降解速率分别为 6.3±0.4 和 2.0±0.1 核苷酸(nt)s-1。这些结果为 MGME1 更强的 5'方向性提供了直接证据,与它在维持线粒体 DNA 中的作用一致。重要的是,当我们使用 NISP 研究绿豆核酸酶(一种 ss 特异性内切酶)时,我们观察到明显不同的 NISP 模式,表明该酶具有分布性切割活性。此外,我们应用 NISP 来确定双链特异性外切酶 λ外切酶的 ssDNA 降解行为。这些发现强调了 NISP 能够准确可靠地测量外切酶和内切酶对 ssDNA 的降解。在这里,我们证明了 NISP 是一种强大的工具,可用于在单分子水平上研究核酸酶的 ssDNA 降解行为。