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Mycobacterium tuberculosis Rv 2991 recombinant protein, preparation method and application of mycobacterium tuberculosis Rv 2991 recombinant protein

A technology of Mycobacterium tuberculosis, rv2991, applied in the direction of botany equipment and methods, biochemical equipment and methods, applications, etc., can solve the problem of low diagnostic value, achieve high stability, reduce production costs, and high sensitivity Effect

Inactive Publication Date: 2015-12-09
SHANGHAI JIAO TONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, PPD has cross-reactions with environmental mycobacteria and BCG vaccine strains, so the diagnostic value is low

Method used

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  • Mycobacterium tuberculosis Rv 2991 recombinant protein, preparation method and application of mycobacterium tuberculosis Rv 2991 recombinant protein
  • Mycobacterium tuberculosis Rv 2991 recombinant protein, preparation method and application of mycobacterium tuberculosis Rv 2991 recombinant protein
  • Mycobacterium tuberculosis Rv 2991 recombinant protein, preparation method and application of mycobacterium tuberculosis Rv 2991 recombinant protein

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Experimental program
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Embodiment 1

[0037] Construction of embodiment 1 recombinant plasmid pET28a-Rv2991

[0038] (1) Target gene primer design

[0039] Rv2991-F (SEQ ID No: 3): GGAATTCCATATGGGAACCAAACAGCGCGC

[0040] Rv2991-R (SEQ ID No: 4): CCCAAGCTTGGCTACGGGGCGGTCGAGCCAC

[0041] The enzyme cutting sites are NdeI and HindIII respectively.

[0042] (2) PCR amplification, cloning and sequence determination of the target gene

[0043] Mycobacterium tuberculosis H 37Rv genomic DNA was used as a template, Rv2991-F and Rv2991-R were used as primers, and the Rv2991 protein gene was directly amplified by PCR using Taq enzyme (Bao Biological Engineering (Dalian) Co., Ltd.). PCR reaction conditions: pre-denaturation at 94°C for 5 minutes; (94°C, 30s; 58°C, 30s; 72°C, 40s) 35 cycles; extension at 72°C for 5 minutes; storage at 4°C. After the reaction, the target fragment was separated by 1% agarose gel electrophoresis, and then recovered with a DNA recovery kit (Invitrogen). Digested with NdeI and HindIII, and cl...

Embodiment 2

[0044] Example 2 Induced expression and purification of recombinant protein Rv2991

[0045] The eppdorf tube containing 100 μl of BL21(DE3) physS competent cells (TIANGEN) was immediately placed on ice from the -80°C freezer. After 3-5 minutes, wait for the liquid in the tube to melt, put 0.5 μl of the recombinant pET32a-Rv2991 plasmid with correct sequencing into competent cells, place it on ice for 45 minutes, place it in a water bath at 42°C, heat shock it for 90 seconds, and let it stand on ice for 3 minutes. Add 500 μl of preheated LB medium without antibiotics, shake at 37°C, 220rmp, and incubate for 45-60min. Take a certain amount and spread it on a solid LB medium plate containing kanamycin, dry it at room temperature and place it upside down in a 37°C incubator for overnight cultivation. Pick the clones, put them into LB liquid medium containing 50μg / ml kanamycin resistance, culture at 220rmp, 37°C to OD to about 0.6, add the final concentration of 10mMIPTG, 37°C for...

Embodiment 3

[0047] Example 3 Recombinant Rv2991 antigen is used as a detection reagent to detect clinically suspected tuberculosis patients

[0048] In this example, the recombinant Rv2991 antigen is used as a detection reagent to detect clinically suspected tuberculosis patients, and healthy people are used as a control group. At the same time, the experiment is carried out in groups with commonly used tuberculosis diagnostic antigens. The ELISPOT test design of specific antigens is shown in Table 1. The operation steps are as follows :

[0049] 1. Sample collection: Aseptically collect about 5ml of human peripheral venous blood into a heparin anticoagulant tube. After collection, the sample can be stored at room temperature, and should not be placed in a refrigerator or freezer; and marked;

[0050] 2. Separation, collection and counting of peripheral blood mononuclear lymphocytes:

[0051] a. Take 5ml of whole blood, add an equal volume of RTPMI-1640 serum-free culture medium, and mix...

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Abstract

The invention discloses a mycobacterium tuberculosis Rv 2991 recombinant protein, a preparation method and application of the mycobacterium tuberculosis Rv 2991 recombinant protein. The mycobacterium tuberculosis Rv 2991 recombinant protein disclosed by the invention has an amino acid sequence shown as SEQ ID NO. 1. The invention also provides the preparation method of a coded nucleotide sequence of the mycobacterium tuberculosis Rv 2991 recombinant protein and the recombinant protein. Based on a research result of immunomics, a mycobacterium tuberculosis immunodominant antigen Rv 2991 is reported for the first time. By applying the mycobacterium tuberculosis Rv 2991 recombinant protein to a tuberculosis cellular immunology diagnosis, higher sensitivity is achieved, and the recombinant protein has the advantages of higher speed, safety and reliability in comparison with a conventional skin test.

Description

technical field [0001] The invention belongs to the technical field of biomedical in vitro diagnostic reagents, and in particular relates to Mycobacterium tuberculosis Rv2991 recombinant protein, a preparation method and application thereof. Background technique [0002] Tuberculosis is caused by the pathogen Mycobacterium tuberculosis infecting the body, and it is still an important infectious disease for humans. Rapid and accurate diagnosis of Mycobacterium tuberculosis (MTB) infection is of great significance for the control of tuberculosis. There are many methods for diagnosing MTB infection. The most commonly used clinical method still relies on traditional sputum smear bacteriological examination, but the detection rate is low; MTB culture can be used as the "gold standard" for the diagnosis of tuberculosis, but the culture time is too long. Generally 4-6 weeks, it is difficult to meet the clinical needs; Bactec technology shortens the culture time, but the cost is hi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07K14/35C12N15/31C12N15/70G01N33/68G01N33/569
CPCC07K14/35G01N33/5695G01N33/68G01N2333/35
Inventor 李荣秀张舒林马国荣张康周福强孙战强
Owner SHANGHAI JIAO TONG UNIV
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