Genome Center, Department of Pharmacology, University of California, Davis, CA 95616, USA.
Nucleic Acids Res. 2011 Mar;39(5):e29. doi: 10.1093/nar/gkq1214. Epub 2010 Dec 5.
The visual detection of specific double-stranded DNA sequences possesses great potential for the development of diagnostics. Zinc finger domains provide a powerful scaffold for creating custom DNA-binding proteins that recognize specific DNA sequences. We previously demonstrated sequence-enabled reassembly of TEM-1 β-lactamase (SEER-LAC), a system consisting of two inactive fragments of β-lactamase each linked to engineered zinc finger proteins (ZFPs). Here the SEER-LAC system was applied to develop ZFP arrays that function as simple devices to identify bacterial double-stranded DNA sequences. The ZFP arrays provided a quantitative assay with a detection limit of 50 fmol of target DNA. The method could distinguish target DNA from non-target DNA within 5 min. The ZFP arrays provided sufficient sensitivity and high specificity to recognize specific DNA sequences. These results suggest that ZFP arrays have the potential to be developed into a simple and rapid point-of-care (POC) diagnostic for the multiplexed detection of pathogens.
特定双链 DNA 序列的可视化检测在诊断学的发展中具有巨大的潜力。锌指结构域为创建能够识别特定 DNA 序列的定制 DNA 结合蛋白提供了强大的支架。我们之前已经证明了 TEM-1 内酰胺酶(SEER-LAC)的序列启用重组,该系统由两个与工程锌指蛋白(ZFPs)相连的失活的内酰胺酶片段组成。在这里,SEER-LAC 系统被应用于开发 ZFP 阵列,该阵列用作简单的设备来识别细菌双链 DNA 序列。ZFP 阵列提供了一个检测限为 50 fmol 靶 DNA 的定量测定。该方法可以在 5 分钟内区分靶 DNA 和非靶 DNA。ZFP 阵列具有足够的灵敏度和高特异性,可以识别特定的 DNA 序列。这些结果表明,ZFP 阵列有可能被开发成一种简单、快速的即时检测(POC)诊断方法,用于对病原体进行多重检测。