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

A method for isolating and purifying native protease 3 from azurophilic granules of human blood neutrophils

A technology for separation and purification of neutrophils, applied in the field of medical detection products, can solve the problems of cumbersome chromatographic column separation steps, impact on yield and purity, loss, etc., to increase enrichment and relative purity, and improve extraction process. , the effect obtained efficiently

Active Publication Date: 2021-04-13
武汉博百欧生物科技有限公司
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Yield and purity are severely affected due to the crude whole cell extract containing a large amount of impurity proteins, the required chromatographic column separation steps are cumbersome, and there is a large amount of loss

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 method for isolating and purifying native protease 3 from azurophilic granules of human blood neutrophils
  • A method for isolating and purifying native protease 3 from azurophilic granules of human blood neutrophils
  • A method for isolating and purifying native protease 3 from azurophilic granules of human blood neutrophils

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0043] The existing preparation and purification process of natural protease 3 (PR3) has more impurity proteins in the blood neutrophil crude extract due to the unreasonable extraction process of primary white blood cell tissue fluid, and the insufficient chromatographic steps lead to a complete The impurity proteins in the crude cell extract cannot be separated well, resulting in the final yield, purity and specificity of native protease 3 being seriously affected. The present invention aims at the problems existing in the existing human blood protease 3 purification method, in order to obtain high-purity, high-activity and high-specificity natural protease 3 antigens in large quantities, through the research on the biochemical characteristics of natural protease 3 (PR3), design An improved method for isolating and purifying native proteinase 3 (Proteinase 3, PR3) from azurophilic granules of human blood neutrophils. The first purpose of this method is to improve the extracti...

Embodiment 1

[0049] In this example, 30.5 g of neutrophil azurophilic granules recovered and extracted from discarded medical supplies after human blood transfusion were used, ground, dissolved, and centrifuged to obtain a chromatographic initial protein solution containing protease 3, which was combined with A series of chromatographic methods such as cation exchange chromatography, dye ligand chromatography, molecular sieve chromatography and affinity chromatography finally obtained 35.0 mg of high-purity PR3 antigen. The specific implementation steps are as follows:

[0050] 1. Use PBS buffer solution to elute the white blood cells in the discarded medical supplies after human blood transfusion, centrifuge the eluate, discard the supernatant and keep the lower cell layer, add cell lysate to the cell layer and centrifuge, keep the lower layer of sediment, and then get astrocytosis Blue granule cell tissue. The azurophilic granulosa cell tissue is rich in proteinase 3. The centrifugatio...

Embodiment 2

[0059] In this example, the purity of the natural protease 3 antigen extracted and purified in Example 1 was verified, and the protease 3 antigen purified by India Yashraj Biotechnology Company was used for parallel comparison. The verification method is polyacrylamide gel electrophoresis (SDS-PAGE), Coomassie blue staining, and then densitometry analysis (Densitometry Analysis) of the electrophoresis gel results after scanning with BioRad's ChemiDoc MP imager. The test results are attached Figure 11 shown. From attached Figure 11 It can be clearly seen from the protein glue shown that the proteinase 3 antigen extracted and purified from Example 1 has higher purity and thermal stability than the product of Yashraj Biotechnology Company in India.

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 present invention provides a method for isolating and purifying natural protease 3 from neutrophil azurophilic granules in human blood. Particles, after grinding, dissolving and centrifuging, obtain the initial protein solution containing protease 3 through chromatography, combined with cation exchange chromatography column, dye ligand chromatography column, molecular sieve chromatography column and affinity chromatography column and other purification methods Isolation and purification of native protease 3 from neutrophil azurophilic granules in human blood. The yield, purity, activity, specificity and stability of the natural protease 3 prepared by the above method are greatly improved, and its high quality is more suitable for scientific research and medical testing.

Description

technical field [0001] The invention relates to the technical field of medical testing products, in particular to a method for separating and purifying natural protease 3 from azurophilic granules of human blood neutrophils. Background technique [0002] Antineutrophil cytoplasmic antibodies (ANCA) are found in necrotizing vasculitis. Most of these antibodies belong to the IgG type, and there are obvious positive reactions in the indirect immunofluorescence reaction of ethanol-fixed neutrophils and monocytes. One of their main targets is the proteinase 3 (PR3) antigen (the so-called cytoplasmic cANCA). Anti-proteinase 3 (PR3)-specific antibody is a sensitive and specific marker of neutrophil-specific autoantibody-associated vasculitic diseases, especially Wegener's granulomatosis (Wegener's granulomatosis), which can help Clinicians diagnose a variety of systemic inflammatory diseases. The antibody is more than 90% specific in patients with active Wegener's granulomatosis...

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): C12N9/64
CPCC12N9/6421
Inventor 孙鹏康雅明
Owner 武汉博百欧生物科技有限公司
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