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Nucleic acid testing method based on prokaryotic Argonaute protein and application of nucleic acid testing method

A nucleic acid and target nucleic acid technology, applied in the biological field

Active Publication Date: 2018-11-13
JIAOHONG BIOTECHNOLOGY (SHANGHAI) CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there is still a lack of methods for rapid and effective detection of target DNA (especially trace DNA)

Method used

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  • Nucleic acid testing method based on prokaryotic Argonaute protein and application of nucleic acid testing method
  • Nucleic acid testing method based on prokaryotic Argonaute protein and application of nucleic acid testing method
  • Nucleic acid testing method based on prokaryotic Argonaute protein and application of nucleic acid testing method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0158] Preparation of detection reagent and detection method

[0159] In this embodiment, a kit for the nucleic acid detection method based on the gene editing enzyme Pyrococcus furiosus Argonaute (PfAgo) of the present invention and its usage method are provided.

[0160] 1.1 Detection reagents and kits

[0161] In this embodiment, taking the detection of the E545K mutation of the PIK3CA gene as an example, the corresponding specific target nucleic acid sequence is 5'-CTGTGACTCCATAGAAAAATCTTTCTCCTGCTCAGTGATTTCAGAGAGAGGATCTCGTGTAGAAATTGCTTTGAGCTGTTCTTTGTCATTTTCCCCT-3', SEQ ID No.: 1.

[0162] Based on the method of the present invention, the corresponding detection reagents include the following:

[0163] (1), amplification primer F-primer and R-primer, specific sequence is as follows:

[0164] F-primer: 5'-CTGTGACTCCATAGAAAATCTTTCTCC-3' (SEQ ID No.2)

[0165] R-primer: 5'-AGGGAAAATGACAAAGAACAGCTC-3' (SEQ ID No.3)

[0166] (2), specific guide ssDNAs pair, including sense s...

Embodiment 2

[0182] Detection of different concentrations of nucleic acids to be detected

[0183] The specific target nucleic acid (SEQ ID NO.: 1) was diluted according to the principle of 10-fold dilution method, and diluted into standard mother solutions of 200pM, 20pM, 2pM, 200fM, 20fM, 2fM and OfM respectively. Nucleic acid standard mother solutions of different concentrations were added to the reaction system described in Example 1, and the sample addition reaction was carried out step by step, and the fluorescent signal value at the wavelength of the corresponding fluorophore was detected by fluorescent quantitative PCR.

[0184] The result is as Figures 4A-4H shown. in, Figure 4A , 4B The concentration of the target nucleic acid in , 4C, 4D, 4E, 4F, 4G is 0fM, 2fM, 20fM, 200fM, 2pM, 20pM, 200pM respectively, Figure 4H It is a non-target nucleic acid (20ng is added to the system).

[0185] Non-target nucleic acid is the total DNA extracted from normal human serum. The resul...

Embodiment 3

[0188] Specificity tests and multiplexing

[0189] Prepare different types of target nucleic acid solutions with a concentration of 200pM, which are two types of HCV virus, JFH-1 2a and CON1-1b.

[0190] It should be noted that the difference between the two types is only that there are two consecutive differences in the sequence.

[0191] Configure a multiplex mixed detection system: add 2 pairs of specific amplification primers to the detection amplification system at the same time, and add the target detection nucleic acid to the detection amplification system in the following 4 groups: (1) blank control; (2) JFH- 12a; (3) CON1-1b; (4) JFH-1 2a and CON1-1b. (The specificity of the fluorescent reporter nucleic acid is verified respectively in Figure 5, and they do not affect each other in a reaction system)

[0192] After the amplification reaction, the PfAgo enzyme, MnCl 2 , 2 groups of specific ssDNAs, 2 pairs of fluorescent reporter nucleic acids with different fluores...

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Abstract

The invention provides a nucleic acid testing method based on a prokaryotic Argonaute protein and an application of the nucleic acid testing method, and particularly provides a system for detecting atarget nucleic acid molecule. The system comprises guide ssDNAs, gene editing enzyme Pyrococcus furiosus Argonaute (PfAgo) and a fluorescence reporter nucleic acid. The nucleic acid testing method ishigh in sensitivity, good in specificity and high in flux and can be widely applied to the fields of molecular medical diagnosis, food safety testing, environmental monitoring and the like.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to a prokaryotic Argonaute protein-based nucleic acid detection method and application thereof. Background technique [0002] Nucleic acid detection technology is widely used in many fields such as molecular medical diagnosis, food safety detection and environmental monitoring. Rapid, cheap and sensitive nucleic acid detection can be widely used in pathogen detection, genotyping, disease course monitoring, etc. [0003] Although some traditional nucleic acid detection methods (qPCR, sequencing, nucleic acid imprinting, etc.) have been widely used, however, there are still some shortcomings. For example, qPCR and high-throughput sequencing have disadvantages such as time-consuming, high cost, and complicated design principles. In addition, for the extremely small amount of nucleic acid to be detected, there is still a lack of satisfactory detection methods in the art. [0...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/44G01N21/64
CPCG01N21/6428C12Q1/44C12Q1/6818C12Q1/708C12Q2521/301C12Q2563/107
Inventor 冯雁荀冠华刘倩
Owner JIAOHONG BIOTECHNOLOGY (SHANGHAI) CO LTD
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