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

Monoclonal antibody YG11-1 of anti-staphylococcus aureus enterotoxin B and applications of antibody

A technology of antibody and sequence table, applied in application, antibody, antibacterial drug, etc., can solve the problem that there is no SEB poisoning vaccine and drug, achieve high affinity and improve survival rate

Active Publication Date: 2020-06-26
ACADEMY OF MILITARY MEDICAL SCI
View PDF5 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there is no effective vaccine and drug against SEB poisoning clinically

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
  • Monoclonal antibody YG11-1 of anti-staphylococcus aureus enterotoxin B and applications of antibody
  • Monoclonal antibody YG11-1 of anti-staphylococcus aureus enterotoxin B and applications of antibody
  • Monoclonal antibody YG11-1 of anti-staphylococcus aureus enterotoxin B and applications of antibody

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Embodiment 1, the preparation of His-SEB protein and its functional research

[0040] 1. Preparation of His-SEB protein

[0041] 1. Replace the small fragment between the NdeI and XhoI restriction sites of the vector pET28a(+) with the DNA molecule shown in sequence 6 of the sequence listing to obtain the recombinant plasmid pET28a-SEB. Sequencing verified.

[0042] In the recombinant plasmid pET28a-SEB, the DNA molecule shown in sequence 6 in the sequence table is fused with the DNA molecule encoding His tag on the vector backbone to form a fusion gene to express the fusion protein.

[0043] The fusion gene is composed of the following two segments sequentially from upstream to downstream: the DNA molecule shown in sequence 8 in the sequence listing, and the DNA molecule shown in sequence 6 in the sequence listing.

[0044] The fusion protein consists of the following two segments sequentially from the N-terminal to the C-terminal: the segment shown in sequence 7 of ...

Embodiment 2

[0073] Embodiment 2, phage antibody library screening anti-SEB protein monoclonal antibody

[0074] 1. Biopanning of anti-SEB monoclonal antibodies

[0075] (1) SEB group

[0076] 1. The first round of affinity panning

[0077] (1) Coat the immunotube with 500 μL of His-SEB protein solution (adjust the protein concentration with PBS buffer) with a protein concentration of 10 μg / mL, and overnight at 4°C.

[0078] (2) Take the immunotube, add PBST buffer solution containing 5g / 100mL skimmed milk powder, and block at room temperature for 1 hour.

[0079] (3) Take the phage antibody library, add PBST buffer containing 5g / 100mL skimmed milk powder, and block at room temperature for 1 hour.

[0080] (4) Take the immune tube that completed step (2), first add sterile PBS buffer to wash 3 times, and then add the phage antibody library that completed step (3) (the input amount of phage is about 1.2×10 12 ), let stand at room temperature for 1h.

[0081] (5) After completing step (...

Embodiment 3

[0101] Example 3, Functional Identification of YG11-1 Antibody

[0102] 1. Preparation of YG11-1 antibody

[0103] 1. Construction of recombinant plasmids

[0104]The small fragment between the HindIII and XhoI restriction sites in the vector pCDNA3.1(+) was replaced with the DNA molecule shown in Sequence 2 of the sequence listing to obtain the heavy chain expression vector. In sequence 2 of the sequence listing, nucleotides 1-584 constitute a promoter, nucleotides 681-2108 encode a full-length heavy chain, and nucleotides 2141-2196 constitute a terminator.

[0105] The small fragment between the HindIII and XhoI restriction sites in the vector pCDNA3.1(+) was replaced with the DNA molecule shown in Sequence 4 of the sequence listing to obtain the light chain expression vector. In sequence 4 of the sequence listing, nucleotides 1-584 constitute a promoter, nucleotides 681-1385 encode a full-length light chain, and nucleotides 1418-1473 constitute a terminator.

[0106] 2. ...

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

PropertyMeasurementUnit
affinityaaaaaaaaaa
Login to View More

Abstract

The invention discloses a monoclonal antibody YG11-1 of anti-staphylococcus aureus enterotoxin B and applications of the antibody. The IgG antibody (named as YG11-1 antibody) consists of a light chainand a heavy chain; the variable region of the heavy chain in the heavy chain consists of 21-145 amino acid residues from the N-terminal of a sequence 1 of a sequence table; and the variable region ofthe light chain consists of 21-127 amino acid residues from the N-terminal of a sequence 3 of the sequence table. The applications of the YG11-1 antibody in preparing drugs for treating enterotoxin B, the applications of the YG11-1 antibody in preparing drugs for antagonizing the enterotoxin B and the applications of the YG11-1 antibody in preparing drugs for preventing and / or treating diseases caused by staphylococcus aureus are also protected. The YG11-1 antibody has important application prospects on treating enterotoxin B poisoning and preventing or treating the diseases caused by the staphylococcus aureus.

Description

technical field [0001] The invention belongs to the field of biotechnology, and specifically relates to a monoclonal antibody YG11-1 against Staphylococcus aureus enterotoxin B and its application, in particular to the preparation of the monoclonal antibody for preventing and / or treating Staphylococcus aureus-induced application in medicine for diseases. Background technique [0002] Staphylococcus aureus (Staphylococcus aureus) is a Gram-positive pathogenic bacteria widely distributed in nature. It is estimated that 20-30% of the population carries the pathogen, which mainly exists in the mucous membranes, skin, and especially the nasopharynx of the human body. Staphylococcus aureus can cause a range of diseases, from minor skin infections, to scalded skin syndrome, to abscesses, to life-threatening pneumonia, meningitis, endocarditis, osteomyelitis, toxic shock syndrome, etc. . Staphylococcus aureus infection affects a wide range of skin, soft tissue, respiratory tract,...

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 Applications(China)
IPC IPC(8): C07K16/12C12N15/13A61K39/40A61P31/04
CPCC07K16/1271A61P31/04C07K2317/92A61K2039/505
Inventor 杨光刘成华刘玉刘方杰高亚萍冯健男
Owner ACADEMY OF MILITARY MEDICAL SCI
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