Method for detecting new coronavirus SARS-CoV-2 N protein by adopting nucleic acid aptamer

A nucleic acid aptamer, sars-cov-2 technology, applied in the field of detection of the new coronavirus SARS-CoV-2 N protein, it can not solve the problem, false negative and false positive results are likely to be produced, and clinical laboratories are widely carried out Difficulties, technical and facility requirements, etc., to achieve the effect of strong affinity, easy preparation, low immunogenicity and toxicity

Pending Publication Date: 2020-09-22
SUZHOU UNIV +1
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Problems solved by technology

[0004] However, each detection method has its disadvantages: 1. Virus isolation and cultivation: The isolation, cultivation and identification of viruses is the gold standard for virus diagnosis, but its methods are complicated, require high technology and facilities, and take a long time. There are difficulties in widespread implementation; 2. Immunological techniques: At present, the new clinical guidelines point out that the detection of new coronavirus-specific IgM in patients begins 3 to 5 days after onset
IgG is even later, starting to appear on 10-21 days, and it will increase 4 times in the recovery period, so this method can only be used for the diagnosis of

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  • Method for detecting new coronavirus SARS-CoV-2 N protein by adopting nucleic acid aptamer
  • Method for detecting new coronavirus SARS-CoV-2 N protein by adopting nucleic acid aptamer
  • Method for detecting new coronavirus SARS-CoV-2 N protein by adopting nucleic acid aptamer

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[0031] The technical solutions in the embodiments of the present invention will be described clearly and completely below. Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative work shall fall within the protection scope of the present invention.

[0032] 1. The homology analysis of the N protein of SARS and SARS-CoV-2

[0033] Using bioinformatics methods and bioinformatics comparisons, it was found that the N protein of the 2003 SARS virus and the 2019 new coronavirus SARS-CoV-2 had 91% protein homology. Molecular structure simulation also speculated that the N protein of SARS-CoV-2 has a similar 3D molecular structure to the N protein of SARS. The homology comparison results of the N protein of SARS-CoV and SARS-CoV-2 are as follows figure 1 Shown.

[0034] 2. Design a...

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Abstract

The invention discloses a method for detecting a new coronavirus SARS-CoV-2 N protein by adopting a nucleic acid aptamer. The aptamer is N Aptamer 1, N Aptamer 2 or N Aptamer 3, can be specifically combined with SARS-CoV-2 virus N protein, and can also be used for specifically detecting N protein diluted in human serum and N protein in a protein electrophoresis sample. By means of the mode, nucleic acid extraction or antibody detection is not needed, meanwhile, the method has the advantages of being high in affinity with target molecules, high in specificity, easy to prepare, low in immunogenicity and toxicity, stable in chemical structure and the like, and conditions are created for early detection of 2019 SARS-CoV-2 pathogens.

Description

technical field [0001] The invention relates to the technical field of biomedical applications, in particular to a method for detecting the N protein of the new coronavirus SARS-CoV-2 using a nucleic acid aptamer. Background technique [0002] The novel coronavirus, with its high infectivity and strong pathogenicity, quickly caused a pandemic of new coronary pneumonia around the world, posing a serious threat to human health and social economy. Rapid and accurate diagnosis of suspected cases, effective isolation of infected persons and active treatment are important foundations for epidemic prevention and control. [0003] At present, the routine methods used in virological diagnosis include: 1. Virus isolation and culture (gold standard for virus characteristics, morphology, staining and biochemical identification); 3. Molecular biology techniques (nucleic acid molecular hybridization, PCR, nucleic acid sequencing, etc.). [0004] However, each detection method has its di...

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Application Information

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IPC IPC(8): G01N33/68G01N33/569G01N33/53
CPCG01N33/68G01N33/56983G01N33/5308G01N2333/165Y02A50/30
Inventor 戴建锋陈志强陈静吴奇涵倪晓华
Owner SUZHOU UNIV
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