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Aflatoxin m1 nanobody 2014AFM-g2

a nano-body and aflatoxin technology, applied in the field of aflatoxin m1 nano-body 2014afmg2, can solve the problems of large reagent consumption, tedious operation, strict limit of aflatoxin m1 in dairy products, etc., and achieve good stability

Active Publication Date: 2015-10-01
INST OF OIL CROPS RES CHINESE ACAD OF AGRI SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0023]Certain embodiments of the present invention, among other things, have the following beneficial advantages.
[0024](1) The construction method of the aflatoxin nanobody gene library described in the present invention is simple. The aflatoxin M1 nanobody 2014AFM-G2 obtained via screening has the properties of tolerance to organic reagents, tolerance to high temperature, tolerance to acids and bases, and good stability.
[0026](3) The aflatoxin M1 nanobody 2014AFM-G2 provided by the present invention can be applied in ELLSA detection of aflatoxin M1 and can effectively reduce the interference by other ingredients such as the organic reagents in the extracting solution of the sample, thus improving the detection accuracy.
[0027](4) The aflatoxin M1 nanobody 2014AFM-G2 provided by the present invention is expressed by prokaryote Escherichia coli, and therefore the production cost of the antibody can be effectively reduced.

Problems solved by technology

Since dairy products are the main source of infant foods, the problems about the aflatoxin M1 contamination have attracted worldwide attention and the amount of aflatoxin M1 is strictly limited in those dairy products.
The chemical analysis method does not need special instruments and equipment and can be carried out in ordinary laboratories, but it has the problems of large reagent consumption, tedious operation, severe interference by other components, poor accuracy, incapability of accurate quantification, great harm to experimenters and surrounding environment, and inapplicability to in-field rapid detection.
The precision instrument analysis methods have high sensitivity and good accuracy, but the instruments therefor are expensive.
Further, those methods require a high purification of aflatoxin samples, require tedious sample pretreatment procedures, are long time consumption, require high standard of experimental environment, and are difficult to realize rapid detection.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

Construction of an Aflatoxin Nanobody Gene Library

[0031]1. Immunization of Animals

[0032]One male alpaca of 2 years old was purchased and immunized with the aflatoxin M1 complete antigen (AFM1-BSA, Sigma-Aldrich Corporation). 200 μg of aflatoxin M1 complete antigen was emulsified with Freund's incomplete adjuvant, and subcutaneously injected to the alpaca at multiple points. The alpaca was immunized in an interval of 2 weeks. Blood was sampled intravenously from the alpaca 7-10 days after each immunization, and serum titer was determined using an indirect ELISA method. After selecting an immunization with the highest titer, 10 mL of blood was sampled for extracting the total RNA.

[0033]2. Construction of a cDNA Library

[0034](1) Extraction of the total RNA: after selecting an immunization with the highest serum titer in the alpaca, and 7-10 days after immunization, 10 mL of blood was sampled intravenously from the alpaca for extracting total RNA: the total RNA was extracted from the bl...

example 2

Screening and Sequencing of Aflatoxin M1 Nanobodies

[0050]1. Panning of Aflatoxin M1 Nanobodies

[0051]ELISA plates were coated with AFM1-BSA (1 μg / well) and 3% of BSA-PBS solution (used as the negative control) respectively at 4° C. overnight. In the next day, the coating solutions were poured off, the plates were washed with PBST for 3 times, and blocked with 3% skimmed milk powder for 1 h. The plates were washed with PBST for 3 times, 50 μl of the above-mentioned rescued aflatoxin nanobody gene library was added to the wells coated with AFM1-BSA, and incubated at 37° C. for 1 h. The plates were washed with PBST for 10 times, 100 μl 100 ng / mL AFM1 solution was added to each well, and eluting is performed via shaking at room temperature (20° C.-30° C.) for 30 min. The eluate was transferred to the wells coated with 3% BSA-PBS solution and incubated at 37° C. for 1 h (removing non-specific adsorption). After incubation, the supernatant was taken to infect with 2 mL of TG1 bacterial cul...

example 3

Preparation of Aflatoxin M1 Nanobody 2014AFM-G2

[0058](1) TG1 bacterial culture capable of secreting aflatoxin M1 nanobody 2014AFM-G2 was obtained, DNA mini-extraction kit of Qiagen was used to extract plasmids. The extracted plasmids were transformed to HB2151 competent cells, and the transformed competent cells were spread onto LB-ampicillin plates.

[0059](2) HB2151 colonies containing aflatoxin M1 nanobody 2014AFM-G2 plasmids were picked out and inoculated onto 100 mL SB-ampicillin liquid culture medium. The inoculated culture medium was cultured under 250 rpm at 37° C. until OD600=0.5-0.8, and 200 μl 0.5 M IPTG solution was added to the culture to induce overnight.

[0060](3) The cultured medium after induction was centrifuged at 4° C. under 10,000 rpm for 15 min. The supernatant was removed carefully in a sterile operation platform, and the bacterial cell pellets were subjected to soluble protein extraction using an osmotic shock method to obtain the proteins from the supernatant. ...

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Abstract

Aflatoxin M1 nanobody 2014AFM-G2 has the amino acid sequence of SEQ ID NO:7, and is encoded by the gene sequence of SEQ ID NO:8. The aflatoxin M1 nanobody 2014AFM-G2 obtained via screening has the properties of tolerance to organic reagents, tolerance to high temperature, tolerance to acids and bases and the like, and good stability. The aflatoxin M1 nanobody 2014AFM-G2 has 50% inhibiting concentration IC50 to aflatoxin M1 of 0.208 ng / mL, and has cross reaction rates with aflatoxin B1, B2, G1, G2 are 9.43%, 5.93%, 4.87% and 6.17%, respectively.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This non-provisional application claims priority under 35 U.S.C. §119(a) on Patent Application No. 201410121773.5 filed in P.R. China on Mar. 28, 2014, the entire contents of which are hereby incorporated by reference.[0002]Some references, if any, which may include patents, patent applications and various publications, may be cited and discussed in the description of this invention. The citation and / or discussion of such references, if any, is provided merely to clarify the description of the present invention and is not an admission that any such reference is “prior art” to the invention described herein. All references listed, cited and / or discussed in this specification are incorporated herein by reference in their entireties and to the same extent as if each reference was individually incorporated by reference.FIELD OF THE INVENTION[0003]The present invention relates to aflatoxin M1 nanobody 2014AFM-G2.BACKGROUND OF THE INVENTION[0004...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G01N33/569C07K16/14
CPCG01N33/56961C07K16/14C07K2317/569G01N2333/38G01N2469/10C07K2317/565
Inventor LI, PEIWUHE, TINGZHANG, QIZHANG, ZHAOWEIDING, XIAOXIA
Owner INST OF OIL CROPS RES CHINESE ACAD OF AGRI SCI
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