Simple and sensitive detection of deoxyribonucleic acid using a RecA−GFP fusion protein–DNA filament as probe

A simple, rapid and highly sensitive method for detection of double‐stranded DNA (dsDNA) was developed using a novel fluorescence probe composed of a RecA–GFP fusion protein that had specific recognition of ssDNA complexes (RecA–GFP–DNA filament). The RecA–GFP fusion protein not only had strong fluorescence, but could also occur by homologous recombination. In the presence of the target dsDNA, the complementary ssDNA of the RecA–GFP–DNA filaments invaded one end of the dsDNA chain. In addition, the other end of the ssDNA dissociated the RecA–GFP filaments. An assay of the probe showed a linear relationship with dsDNA concentration in the range 1–11 nM, with a correlation coefficient of 0.9923. The limit of detection for dsDNA was determined experimentally to be 0.3 nM (3δ). Compared with conventional methods, this method has the advantages of simple operation, high specificity, and high sensitivity. A simple, rapid and highly sensitive method for the detection of double‐stranded DNA (dsDNA) was developed using the RecA‐ssDNA filament. This method presented high sensitive which could detect dsDNA as low as 0.12 nM, since the recombination of one chain DNA could release several RecA‐GFP fusion proteins to amplify the fluorescence signal. Compared with the conventional methods, This method has the advantages of simple operation, high specificity and high sensitivity.