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用于诊断应用的特定 DNA 序列的可视化检测的锌指蛋白阵列。

A zinc finger protein array for the visual detection of specific DNA sequences for diagnostic applications.

机构信息

Genome Center, Department of Pharmacology, University of California, Davis, CA 95616, USA.

出版信息

Nucleic Acids Res. 2011 Mar;39(5):e29. doi: 10.1093/nar/gkq1214. Epub 2010 Dec 5.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3845/3061069/f0c0dbe1acad/gkq1214f1.jpg

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