Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A mass spectrometry method and application for quantifying nucleic acids based on DNA-polypeptide probe technology

A DNA probe and probe technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve problems affecting PCR amplification efficiency and response, affecting signal collection, deviation, etc., and achieve high accuracy, Detect effects with high specificity and high precision

Active Publication Date: 2021-11-16
GUANGDONG HOSPITAL OF TRADITIONAL CHINESE MEDICINE
View PDF10 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

qRT-PCR requires fewer samples, but qRT-PCR technology usually requires pre-amplification of target RNA and further fluorophore labeling steps, and the background difference between samples will affect the amplification efficiency and response of PCR. Quenching affects signal collection and introduces bias
There is currently no quantitative method that can directly and specifically detect lncRNAs, therefore, it is imperative to develop new strategies that can provide quantitative results of lncRNAs in a sensitive and direct manner

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A mass spectrometry method and application for quantifying nucleic acids based on DNA-polypeptide probe technology
  • A mass spectrometry method and application for quantifying nucleic acids based on DNA-polypeptide probe technology
  • A mass spectrometry method and application for quantifying nucleic acids based on DNA-polypeptide probe technology

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0046] Embodiment 1 Construction of mass spectrometry method based on DNA-polypeptide probe technology quantitative nucleic acid

[0047] This embodiment takes HULC nucleic acid as an example, and provides a mass spectrometry method based on DNA-polypeptide probe technology to quantify HULC. Based on the nucleotide sequence of the nucleic acid to be tested, DNA probes are designed; characteristic polypeptides are screened out, and combined with DNA probe to construct a DNA-polypeptide probe; hybridize the DNA-polypeptide probe with the nucleic acid to be tested; perform proteolysis on the hybridized DNA-polypeptide probe, so that the characteristic polypeptide in the DNA-polypeptide probe is hydrolyzed into a reporter peptide ; Construct the LC-MS / MS detection method of the reporter peptide; use the LC-MS / MS detection method to detect the concentration of the reporter peptide; convert the concentration of the reporter peptide into the copy number of the nucleic acid to be teste...

Embodiment 2

[0220] Example 2 Application of the construction-based nucleic acid mass spectrometry quantitative method in the detection of HULC copy number in hepatocytes

[0221] In this embodiment, five different hepatocytes were used as samples to be tested, and the copy number of HULC was detected. The five kinds of liver cells used were normal liver cell L02, normal liver cell 7702, liver cancer cell SK-Hep1, liver cancer cell HepG 2 , Liver cancer cell 7721.

[0222] Refer to the construction method of the DNA-polypeptide probe in Example 1, the hybridization of the DNA-polypeptide probe and the nucleic acid to be tested, the enzymatic hydrolysis to obtain the characteristic polypeptide reporter peptide, and the LC-MS / MS of the characteristic polypeptide reporter peptide constructed based on Example 1 The detection method is to detect the copy number of HULC in the above five kinds of hepatocytes.

[0223] Wherein, the extraction process of total RNA in the above five kinds of live...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention belongs to the technical field of rapid biological detection, and specifically relates to a mass spectrometry method for quantitative nucleic acid based on DNA-polypeptide probe technology, comprising the following steps: designing a DNA probe based on the nucleotide sequence of the nucleic acid to be tested; screening out the characteristic polypeptide, and construct a DNA-polypeptide probe with the DNA probe; hybridize the DNA-polypeptide probe with the nucleic acid to be tested; carry out proteolysis of the hybridized DNA-polypeptide probe, and decompose the DNA-polypeptide probe in the DNA-polypeptide probe The characteristic peptide is hydrolyzed into a reporter peptide; construct a LC-MS / MS detection method for the reporter peptide; use the constructed LC-MS / MS detection method to detect the concentration of the reporter peptide; convert the concentration of the reporter peptide into the copy number of the nucleic acid to be tested , to realize the quantitative detection of the nucleic acid to be tested. Based on the above method, the conversion of nucleic acid quantification to polypeptide quantification has the advantages of high detection efficiency and strong specificity; in addition, the detection of the liver cancer marker HULC by this method is more conducive to the risk assessment of liver cancer.

Description

technical field [0001] The invention belongs to the technical field of rapid biological detection, and in particular relates to a method and application of lncRNA mass spectrometry quantification based on DNA-polypeptide probe technology. Background technique [0002] Long non-coding RNA (Long non-coding RNA, lncRNA) is a non-coding RNA longer than 200 nucleotides. With the gradual deepening of research, the function of lncRNA has been gradually discovered by researchers, and it is closely related to the occurrence and development of tumors. HULC is the earliest lncRNA found in liver cancer. Studies have found that HULC is significantly elevated in patients with liver cancer, and can participate in the regulation of the molecular mechanism of liver cancer. It is expected to become a potential biomarker for the diagnosis of liver cancer. [0003] At present, the methods for quantitative detection of lncRNA mainly include fluorescent dye method, Northern blot analysis, microa...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/682C12Q1/6886
CPCC12Q1/682C12Q1/6886C12Q2600/178C12Q2521/537C12Q2525/203C12Q2565/627C12Q2563/131C12Q2537/16
Inventor 黄宪章张乔轩蔡志梁韩丽乔严君展敏欧阳芬王建兵柯培锋庄俊华
Owner GUANGDONG HOSPITAL OF TRADITIONAL CHINESE MEDICINE
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com