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


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 ?-lactamase (SEER-LAC), a system consisting of two inactive fragments of ?-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.

SUBMITTER: Kim MS 

PROVIDER: S-EPMC3061069 | biostudies-literature | 2011 Mar

REPOSITORIES: biostudies-literature

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

Kim Moon-Soo MS   Stybayeva Gulnaz G   Lee Ji Youn JY   Revzin Alexander A   Segal David J DJ  

Nucleic acids research 20101205 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 dev  ...[more]

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