EP0553077A1 - Anticorps monoclonaux destines a des insecticides au cyclodiene et procede de detection desdits insecticides - Google Patents
Anticorps monoclonaux destines a des insecticides au cyclodiene et procede de detection desdits insecticidesInfo
- Publication number
- EP0553077A1 EP0553077A1 EP19910905126 EP91905126A EP0553077A1 EP 0553077 A1 EP0553077 A1 EP 0553077A1 EP 19910905126 EP19910905126 EP 19910905126 EP 91905126 A EP91905126 A EP 91905126A EP 0553077 A1 EP0553077 A1 EP 0553077A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- compounds
- cyclodienes
- monoclonal antibodies
- heptachlor
- antigen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/44—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material not provided for elsewhere, e.g. haptens, metals, DNA, RNA, amino acids
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/5308—Immunoassay; Biospecific binding assay; Materials therefor for analytes not provided for elsewhere, e.g. nucleic acids, uric acid, worms, mites
Definitions
- the subject invention is related generally to assay of insecticides found in foods and environmental samples and more particularly to production and use of monoclonal antibodies for specific detection of cyclodiene insecticides.
- cELISA competition enzyme-linked immunosorbent assay.
- BSA bovine serum albumin.
- KLH keyhole limpet hemocyanin
- GC/EC gas chromatography/electron capture
- GABA gamma-amino butyric acid, a neurotransmitter which increases the permeability of the post- synaptic membrane to Cl ⁇ ion.
- hapten a small molecule which carries an antigenie determinant, but is not i munogenic until it is chemically coupled to a larger protein carrier.
- the hapten-carrier complex then stimulates an immune competent cell to form antibodies to the hapten and the complex;
- HPLC high pressure liquid chromatography
- cyclodiene insecticides chlorinated hydrocarbon insecticides, containing an endo ethylene bridge which include heptachlor, chlordane, aldrin, dieldrin, endrin, p
- Strobane endosulfan. toxaphene and BHC (mixed isomers) benzene hydrochloride.
- heptachlor 1 ,-exo-,4,5,6,7,8,8,-Heptachloro-3a,4, 7, 7a-tetrahydro-4,7-methanoindene.
- heptachlor epoxide the product of heptachlor oxidation, which occurs in soil, in animals, and in or on crops when treated with heptachlor.
- chlordane 2,3,4,5,6,7,8,8-Octachloro-2,3,3a,4, 7,7a-hexahydro-4,7-methanoindene.
- aldrin 1 ,2,3,4,10,10-Hexachloro-l ,4,4a,5,8,8a hexahydro-1 ,4-exo, endo-5,8,-dimethano- naphthalene (HHDN).
- dieldrin (1R, 4S, 5S, 8R)-1 ,2,3,4,10,10 -hexachloro-1 ,4,4a,5,8,8a -hexahydro-1 ,4:5,8-dimethano-naphthalene
- endosulfan 6,7,8,9,10,10-Hexachloro-l ,5,5a,6, 9,9a-hexahydro-6,9, -methano-2,4,3-benzoCe3- dioxathiepin-3-oxide.
- endrin (1R, 4S, 5R, 8S) 1 ,2,3,4, 10, 10-hexachloro
- Strobane polychlorinates of camphene, pinene and related terpenes. (Production discontinued by Tenneco Chemicals, Inc.).
- norbornene isomer resulting from the maximal interaction between the unsaturated systems of the reaction between cyclopentadiene and maleic anhydride.
- the acid anhydride ring system is fused to the newly formed methylene-bridged cyclohexene nucleus (bicycloC2.2.13hept-2-ene; norbornene) through its endo positions.
- camphene C- Q H- Q .
- toxaphene (camphechlor) isomeric reaction mixture of chlorinated camphenes containing 67-69% chlorine.
- BHC 1 ,2,3,4,5,6-Hexachlorocyclohexane; also known as benzene hexachloride.
- Kepone Decachloro-octahydro-1 ,3,4,-metheno-2H- cyclobuta(cd) pentalen-2-one (Discontinued by Allied Chemical Co.).
- Cyclodiene insecticides are a large group of polychlorinated cyclic hydrocarbons with endomethylene bridged structures.
- a variety of chlorinated hydrocarbon insecticides were prepared by the Diels-Alder reaction following the discovery of chlordane in 1945, and various derivatives were widely used in the United States and other countries. Until recent discontinuance of production, or limitations on domestic usage, the cyclodiene insecticides most commonly used in the United States were
- Cyclodiene insecticides may have one or more 5 or 6 carbon rings which have been heavily halogenated. Cyclodienes may have a single cyclopentadiene ring or a dicyclopentadiene ring structure.
- the structure of bicyclo[2.2.13hept-2-ene has a joined pair of five carbon rings, which is formed by the joint sharing of three carbons, and is termed the norbornene functionality.
- the norbornene structure is a common structure of many cyclodiene insecticides.
- Cyclodienes may have a dicyclopentadiene (C -Q H, ⁇ ) ring structure in which 3 carbons are shared commonly between two 5 carbon rings and also 2 carbons may be shared commonly between one of those rings and another 5 carbon or substituted five-carbon ring. Each of the ring structures is extensively halogenated. with the ring hydrogens most commonly being replaced with chlorine. Cyclodiene insecticides act upon the central nervous system by inhibition of ATPase activity which affects ion transport and interferes with nerve cell receptors.
- cyclodiene insecticides in use differ widely in their chemical structure, toxicity and photostabiiity.
- Heptachlor was heavily used in agriculture as an insecticide and termiticide until these applications were phased out in the mid-1970's.
- heptachlor use is restricted, however, previous widespread use of these compounds has led to concern about the possibility that pesticide residues might remain in foodstuffs and the environment.
- Antibodies with specific binding to reactive sites on small organic molecules are sensitive indicators, which may distinguish chemical isomers (Stanker et al , Toxicology 45: 229-243 1987). With small haptens, the greatest antibody specificity for a reactive group appears to occur when that reactive group is most distant from the site of the linkage binding to the carrier protein. Previous attempts at immunization have produced polyclonal antibodies which have poor specificity for heptachlor.
- Another object is to provide a method for production of monoclonal antibodies which identify cyclodiene insecticides, particularly those with the cyclopentadiene or dicyclopentadiene functionality, more preferably those with the norbornene structure, and including production of a monoester of heptachlor hapten which will elicit formation of these antibodies.
- a further object is to provide a method for the specific and sensitive detection and separation of cyclodiene insecticides from samples, particularly a class of cyclodiene insecticides which possess the cyclopentadiene or dicyclopentadiene functionality, and more particularly a class of cyclodiene insecticides which possess the norborene structure, by binding to specific monoclonal antibodies.
- Another object is to provide a method for separation of halogenated cyclic organic compounds from tissue or environmental samples and solubilizing them in a vehicle appropriate for assay of halogenated cyclic organic compounds by specific monoclonal antibodies.
- Another object is to provide a method for the detection and isolation of cyclodiene insecticides, particularly those with cyclopentadiene or dicyclopentadiene functionalities, and more particularly those with the norbornene structure, in environmental and food samples.
- the subject invention is directed to the monoclonal antibody, and the hybridoma which produces it, which is specifically reactive to the cyclodienes which have a cyclopentadiene or dicyclopentadiene functionality, and more specifically, to cyclodiene insecticides which have the norbornene structure.
- Such compounds include, but are not limited to those shown in Table 1 (appearing on page 33), and derivatives thereof.
- the present invention also provides a method for the production and use of monoclonal antibodies reactive with the antigenic determinants on compounds selected from the group consisting of the cyclodiene insecticides which have a cyclopentadiene or dicyclopentadiene functionality, or more particularly to those with the norbornene structure.
- the method for the production of monoclonal antibodies to cyclodiene insecticides in accordance with the subject invention is adapted from general methods for production of monoclonal antibodies, such as that described by Kohler and Milstein (1975), which is incorporated by reference.
- Cyclodiene-specific antibodies are produced by immunizing a suitable mammal with an immunogenic carrier protein conjugate of the desired antigen compound and obtaining im unosensitized cells from the mammal, which are capable of producing antibodies to the antigen.
- the immunosensitized cells are fused with immortally reproducing cells of the same species, or of another mammal species.
- hybrid cells produced are cultured in a suitable host, or in a culture medium, and clones of hybrid cells, referred to as hybridomas, are isolated.
- the hybridomas continuously produce specific antibodies which react with the sensitizing antigen and from them cells are selected which produce monoclonal antibodies of desired reactivity. These antibodies are grown in culture medium or in a host, and harvested and purified, if desired.
- the monoclonal antibodies produced are capable of recognizing cyclodiene insecticides, particularly those with the cyclopentadiene or dicyclopentadiene functionalities, and more particularly those with norbornene structure.
- the cell lines developed in accordance with the instant invention are capable of producing highly specific monoclonal antibodies which may be used to distinguish the presence of cyclodiene insecticides in foods and environmental samples. These antibodies are contemplated to be useful for the sensitive detection of cyclodiene insecticides in tissue and surface samples.
- the disclosed cyclodiene insecticide specific antibodies produced according to the present method may be used as attachment agents in an affinity column for the concentration and purification of cyclic pesticide structures which may contain substitutions on the ring structure.
- the subject method of use provides for preparation of samples containing polar soluble compounds so that they may be rapidly and automatically screened for polar compounds, by a nonpolar immunoassay with monoclonal antibodies.
- the procedure for isolation of assay samples is suitable for materials found in environmental samples and in common foods.
- the extraction procedure developed for assay of food or environmental samples by specific monoclonal antibodies may also be used when samples are assayed by GC/EC.
- a kit format of the diagnostic method may be used for field testing of environmental surface wipe samples.
- Figure 1 presents a representative synthetic pathway for the production of the hapten-carrier protein linkage of the immunogen used to immunize mice to produce monoclonal antibodies to cyclodiene insecticides.
- Figure 2 shows representative competition ELISA data for the monoclonal antibody from hybridoma Hept-2, (closed circles) when heptachlor is used as a competitor. Bars represent +/- one standard deviation.
- Figure 3 shows competition ELISA data for monoclonal antibody from Hept-2 when reacted with competitors: heptachlor, (closed circle); heptachlor epoxide, (open circle); aldrin, (open square); chlordane, (open diamond ⁇ : and endrin, (open triangle).
- the subject invention is directed to a group of monoclonal antibodies, and the hybridomas which continuously produce them, which react specifically with the described group of cyclodiene insecticides, which contain the cyclopentadiene or dicyclopentadiene ring, and more particularly to those which contain the norbornene structure.
- the present invention also provides a method for making monoclonal antibodies reactive to chlorinated cyclodiene insecticides with the cyclopentadiene or dicyclopentadiene rings, more particularly to those which contain the norbornene structure.
- the subject invention provides a method for preparation of samples containing fat-soluble halogenated cyclic organic compounds so that they may be assayed by aqueous-based immunoassay.
- Cyclodiene insecticides are small organic molecules, and in order to render them immunogenic, it was necessary to conjugate such molecules to carrier protein by a method such as that described in
- cyclodienes may be made in an effort to achieve this purpose.
- a functional group was introduced into chlordene by which it could be conjugated to a carrier protein.
- hexachlorocyclo- pentadiene and cyclopentadiene are allowed to react together and the resulting intermediate is oxidized to form 1-hydrochlordene.
- This intermediate was connected with a succinate linker to a carrier protein to form the immunogen.
- the carrier protein was selected from any of several immunogenic proteins such as keyhole limpet hemocyanin, serum albumins and thyroglobulin.
- the analog hapten of heptachlor was linked through succinate to BSA as the protein conjugate.
- Immunization to Raise Antibodies Techniques for the immunization of laboratory mammals with proteins are known to those skilled in the art. However, when the antigenic compounds are short peptide fragments or small nonproteinaceous molecules, immunization with these compounds may fail to produce an adequate immune reaction. Modified small molecules, termed haptens, may be conjugated to a known immunogen or to a carrier protein which is a known immunogen and by such a linkage be rendered immunogenic. Mammalian antibodies raised in response to an immunogenic conjugate may recognize the small molecule apart from the carrier protein. Carrier proteins may be selected from any of a group of proteins which are immunogenic.
- Suitable carrier proteins include, but are not limited to, keyhole limpet hemocyanin (KLH), serum albumins, including bovine serum albumin (BSA), globulins including thyroglobulins and the like. Keyhole limpet hemocyanin (KLH) and bovine serum albumin (BSA) are conveniently employed in the subject invention.
- KLH keyhole limpet hemocyanin
- BSA bovine serum albumin
- KLH keyhole limpet hemocyanin
- BSA bovine serum albumin
- the method for the production of monoclonal antibodies which are capable of distinguishing the presence of cyclodiene insecticides with the cyclopentadiene or dicyclopentadiene ring structure and more particularly of distinguishing the presence of cyclodienes with the norbornene structure in accordance with the subject invention, comprises immunizing a suitable mammal, preferably mice, rats, hamsters, rabbits, goats, sheep, cows and horses, still more preferably mice, with an antigen hapten conjugate; preferably with an antigen of heptachlor succinate hapten, which has been conjugated to an immunogenic carrier protein.
- Repeated intraperitoneal (i.p.) administration of the antigen is made to a first species of mammal in a suitable amount, preferably between about 10 ug to about 200 ug, with about 50 ug
- the antigen may be mixed with adjuvant, preferably Ribi adjuvant (Ribi Immunoche ical Research
- Immunosensitized spleen cells or lymphocytes preferably sensitized spleen cells, which are now capable of producing antibodies to the antigen of choice, are removed from the animal.
- the sensitized spleen cells or lymphocytes are fused with immortally reproducing cells, preferably myeloma cells of the first species of mammal or of another species, to produce hybrid cells.
- the hybrid cells are cultured in a suitable host or in a culture medium.
- the clones of hybrid cells, known as hybridomas, which continuously produce or secrete specific antibodies to an antigen of the aforenamed group, are isolated.
- Hybridomas which produce monoclonal antibodies that distinguish the presence of cyclodienes, are selected, quantities of these monoclonal antibodies are generated, antibodies from the culture medium or from the host used for growing the cells are harvested, the monoclonal antibodies isolated and purified, if preferred, and monoclonal antibodies so produced are used to assay samples for the presence of cyclodienes.
- the hybridomas may be propagated in a suitable host animal or grown in a suitable culture or carrier medium.
- Host animals are mammals which include, but are not limited to, those described previously.
- Suitable culture media include, but are not limited to, ascites fluid, hybridoma supernatant or synthetic media, such as D-MEM, RPMI or Iscocos, as well as one of the culture media specified above.
- Antibodies were screened for their ability to bind to the analog hapten of heptachlor-BSA and were also selected for those similarly responsive to the related cyclodiene compounds, heptachlor epoxide, chlordane, aldrin, as well as the synthesized antigen, heptachlor-KLH, but were not responsive to the carrier proteins alone.
- the selection procedure also included screening for antibody which would be active in the solvent system of the immunoassay. This screening eliminates clones that recognize the linkage chemistry of the conjugate protein. Those clones which test positively with respect to the hapten regardless of carrier protein and negative with respect to the two carrier proteins in the presence of immunoassay solvent were subcloned. Those clones which could recognize free heptachlor, heptachlor epoxide and/or chlordane were evaluated by c-ELISA.
- the hybridoma cell line designated as Hept-2, was developed.
- the clone of said cell line is capable of producing monoclonal antibody of high specificity with which to distinguish the presence of the described cyclodienes with the cyclopentadiene or dicyclopentadiene functionality, more preferably to distinguish the presence of the described cyclodienes with the norbornene structure.
- This cell line was deposited on December 11, 1990, with the American Type Culture Collection (ATCC), 12301 Parklawn Drive, Rockville, Maryland 20852 USA, and has been accorded Accession Number ATCC No. HB 10623. This hybridoma deposit was made pursuant to a contract under the terms of the Budapest
- Antibodies of this invention may be used in the form of hybridoma supernatant, or as ascites fluid, or as the isolated and purified monoclonal antibodies.
- the sensitivity of the assey is dependent upon the type of binding antigen used to coat the microtiter plate. Any of the several described cyclodiene antigens may be used to coat the microtiter plate, the preferred antigen being a BSA protein conjugate of heptachlor.
- the binding specificities of antibodies to standards and assay samples were evaluated by competition ELISA assays.
- an antigen which is a large molecule with protein or carbohydrate moieties which can precisely bind with steric interaction with the conformation of the antibodies, is fixed to the reaction surface of a test plate.
- Antigen-specific antibody is added along with an aliquot of sample extract or standard test solution.
- the free-floating antibody partitions between the fixed antigen bound to the test reaction surface and the antigen of the added sample or standard, which is free-floating in the solution.
- the free-floating antigen-antibody complex is washed away.
- the plate is rewashed and incubated with an enzyme-tagged indicator molecule which will immunospecifically bind to the proteins of the animal species which was the source of the cyclodiene-specific antibodies.
- Substrate and buffer are provided for the reaction of the enzyme-tagged indicator molecule.
- the optical signal generated from the enzyme substrate reaction indicates the amount of cyclodiene-specific antibody which remains bound to the immobilized antigen on the reaction plate. Limited color in the microtiter reaction well indicates a high concentration of antigen in the sample. The utility of such a reaction system is dependent on the surface binding of the antigenic hapten-protein complex.
- the sensitivity of such a binding system can be amplified by any of several means such as by coupling the enzyme reaction endpoint to a biotin-avidin complex.
- Optimal enzyme detection sensitivity occurs when a minimal amount of coating antigen (heptachlor-BSA) is used.
- the total binding capacity of the plate is large so that extra unconjugated carrier protein does not degrade binding.
- the present invention also provides an improved method for identifying organic compounds and pesticides in the presence of other compounds found in food or environmental samples.
- the method is contemplated to be useful for the sensitive detection of organic compounds, pesticides and their metabolites in samples by their specific binding affinity to monoclonal antibodies which are fixed to a surface.
- nonpolar compounds non-electrolytic compounds which generally consist of carbon or nitrogen, with or without other elements, are to be assayed by a specific monoclonal antibody in a polar or electrolytic reaction medium of the immunoassay.
- Fat can be removed by rendering of the tissue with heating to 110°C for 30 minutes and extraction of the rendered fat with activated resin, such as silica gel, alumina, C-18 reverse phase resin or florisil, preferably florisil, followed by a resuspension of the sample in a polar-non-polar solvent mixture for immunoassay.
- activated resin such as silica gel, alumina, C-18 reverse phase resin or florisil, preferably florisil
- Food or tissue samples are prepared for assay by heating and dissolving the rendered fat in organic solvent.
- Assay samples from soft samples, such as soils, grains and muscle tissue are ground in organic solvent, such as hexane and subjected to column fractionation. Muscle tissue of fish and other lean animals is homogenized in organic solvent, and milk is simply extracted with an organic solvent, preferably hexane. The hexane-extracted fat fraction is applied to an activated glass column in which the resin is used in a ratio of 50-100 times the weight of the fat sample.
- the fat soluble components are eluted from an activated glass column, preferably a florisil column, with organic solvent such as hexane and the solvent evaporated under a stream of inert gas (N 2 @ 30°C).
- the residues are then resuspended in alcohol, preferably 100% methanol and subsequently diluted to 25% methanol prior to assay with cyclodiene-specific monoclonal antibodies of the invention.
- Other sample preparation techniques when used for HPLC or GC analysis, use a smaller amount of florisil and may leave residues which may interfere with the immunoassay.
- This sample preparation method is suitable for a variety of organic compounds, including those with one or more 5 or 6 carbon ring structures. It is especially suitable for heterocyclic pesticides, their production by-products and metabolites.
- a kit format of the detection system may be used for field analysis of surface wiped or extracted samples.
- the specific antibodies developed here can be used in a diagnostic kit for office or field testing of samples which are suspected of containing cyclodiene insecticides or metabolites of such.
- a card or a cup test format may be used in which the antibody is affixed to an absorbent layer, or is mixed in a permeable layer which is bound to an absorbent layer.
- the binding specificity of the described monoclonal antibodies of this invention for cyclodienes may be utilized in a binding column to selectively discriminate cyclodienes.
- Compounds with the norbornene structure may reversibly bind specifically to monoclonal antibodies, produced by this invention, which are fixed in a column.
- Differential binding of cyclodiene compounds to a column of fixed monoclonal antibody may also be used to remove, purify or concentrate these compounds.
- An exemplary separation method is binding and release of a compound by alteration of the ionic concentration of the column.
- the cyclodiene compound, heptachlor is a small molecule. which by itself has limited immunogenicity.
- a hapten is formed b condensation of hexachloropentadiene and cyclopentadiene to develop an intermediate, chlordene, and oxidation of the intermediate to form 1-hydroxychlordene by the method of Buchel et al . Chem. Ber.
- the 1-hydroxychlordene hapten is rendered immunogenic by coupling it to an immunogenic carrier protein through a succinate moiety.
- the conjugated hapten-protein elicits formation of an antibody which will recognize several different cyclodienes.
- condensation reaction is a Diels-Alder addition of hexachlorocyclopentadiene and cyclopentadiene to yield 4,5,6,7,8,8,-hexachloro-3a,4,
- the hapten was rendered immunogenic by coupling to an immunogenic carrier protein through a succinate moiety.
- an immunogenic carrier protein through a succinate moiety.
- 4,7,7a-tetrahydro-4,7-methanoindene was treated with succinic anhydride in pyridine.
- the resulting solution was evaporated in vacuo, dissolved in 5% aqueous sodium bicarbonate, washed with chloroform, and the aqueous solution was acidified with concentrated hydrochloric acid to give the crude he isuccinate.
- the crude material was conjugated to bovine serum albumin and keyhole limpet hemocyanin by a N-hydroxysuccinimide procedure such as that described by Lauer et al . Experientia 30: 558 (1974), which is incorporated by reference.
- the hapten-protein conjugates used for immunization were produced by conjugation of the 1-hydroxychlordene hemisuccinate to keyhole limpet hemocyanin (KLH) to form (heptachlor-KLH), and to bovine serum albumin (BSA) to form (heptachlor-BSA) using acid anhydride intermediate which readily couples to the free amine groups of the protein.
- KLH conjugates were used for immunization of animals and BSA conjugates were used for ELISA screening of hybridoma clones.
- mice with a heptachlor-keyhole limpet hemocyanin conjugate (heptachlor-KLH).
- heptachlor-KLH heptachlor-keyhole limpet hemocyanin conjugate
- the heptachlor-keyhole limpet hemocyanin conjugate preferably 1-hydroxychlordene-KLH, made as described above, was used to immunize 6-month old BALB/cBkl mice by repeated intraperitoneal injections, preferably three, of 50 ug heptachlor-KLH conjugate, mixed with Ribi adjuvant.
- the mice received a single injection every other week for three injections.
- mouse hapten-specific serum titer was boosted with an intrasplenic injection of 100 ug cyclodiene-bovine serum albumin conjugate, preferably
- Hybridoma fusions, of lymphocytes to SP2/0 myeloma cells were made by standard methods such as those described by Bigbee, W.L. et al . Molecular
- Fusion is not limited to the use of SP2/0 myeloma cells and the use of other immortally reproducing mammalian cells is contemplated to be within the scope of this invention. Following fusion, hybridomas were screened in a direct binding ELISA for the ability of the antibodies which they produced to recognize the appropriate
- a direct binding ELISA assay a modification of the method of Stanker et al . (1986) (0. Immunol. 136: 4174-4180), was used to screen against a variety of heptachlor and heptachlor-related antigens for antibodies to cyclodienes in the culture fluids of growing hybridomas.
- Microliter plates were coated with a cyclodiene hapten-protein complex, preferably 1-hydroxychlordene-bovine serum albumin complex in the amount of about 0.002-0.5 ug per well, preferably about 0.2 ug per well, in carbonate-bicarbonate buffer
- TM surfactant compounds especially preferred was 0.05% Tween-20 (Polyoxethylenesorbitan Monol aurate) i n a concentration of
- a fluorometric endpoint of an enzymatic reaction such as, mouse peroxidase, conjugated with goat anti-mouse antiserum (United
- Hybridoma cells from wells showing a positive response in the ELISA screen were expanded and subcloned twice by limiting dilution to ensure their monoclonal origin.
- Ascites fluid was prepared in irradiated mice according to Stanker et al . (1986) (J.Immunol. Methods 136: 4174-4180), and the monoclonal antibodies purified from the ascites by a method such as hydroxylapatite chromatography as described by (Stanker et al . (1985) J. Immunol .
- Hybridomas from the fusions were cultured and antibodies that recognized both hapten conjugates, but not either carrier protein, was observed and evaluated for their ability to recognize unconjugated heptachlor and heptachlor epoxide in a competition
- Isotype of the monoclonal antibody produced by Hept-2 was determined to be IgG 2a kappa -. ght chain by direct-binding ELISA with isotype-specific antisera (Southern Biotech, Mobile, AL). 5. Assessment of Cyclodienes by Competition Enzyme-linked Immunoabsorbent Assays
- a competition enzyme-linked im unosorbent assay (c-ELISA) was developed to quantify heptachlor standards in solution and to assess the specificity of the antibodies for various cyclodienes and derivatives. Any of several coating antigens were used, however, preliminary work to optimize the sensitivity of the assay showed greatly improved sensitivity if heptachlor-bovine serum albumin was used.
- Microtiter plates were coated with 0.025 ug/well heptachlor-BSA and blocked with 300 ul of assay buffer per well for 1 hour at room temperature. In the competition ELISA, the competitors of antibody binding were dissolved in methanol and were added to assay buffer.
- Competitor was added so that each well contained 100 ul of competitor in a 50% methanol-assay buffer solution.
- An equal volume of assay buffer containing monoclonal antibody was added such that there was a final concentration of 100-200 ng antibody/well in a 25% methanol solution in assay buffer comprising antibody and competitor.
- These antibodies can tolerate up to 40% methanol with only minimal loss of activity.
- Peroxidase-conjugated goat anti-mouse IgG antibody was added. The plates were incubated for one hour at room temperature and the endpoint assessed by observation of the color change of
- ABTS 2,2,azino-di-3-ethylbenzthiozoline sulfonic acid
- avidin (10 /M) forms bridging complexes between biotinylated molecules.
- Both the specific-binding monoclonal antibody and the peroxidase-enzyme indicator system are bound to biotin. Linkage of the biotin molecules with avidin complexes the indicator molecules and increases detection signal.
- Cyclodiene specific antibody was conjugated to biotin by standard methods, such as that described by P. Tijssen in Chapter 3 of "Practice and Theory of Enzyme Immunoassays" (R. H. Burdon and P. H. Van Knippenberg, Eds., Elsevier, Amsterdam (1985)).
- Biotinylated-N-hydroxy succinimide (BNHS) ester was reacted with the cyclodiene-specific antibodies to make the biotinylated i munoreactants.
- cyclodiene-specific antibody was identified by the binding of a biotinylated anti-mouse IgG immunoglobulin to the antibody, and using biotinylated peroxidase, Vectastain (Vector Laboratories, Burlinga e, CA) for bridging to the avidin-biotin amplification complex.
- the antibody of the hybridoma Hept-2 was titrated against immobilized antigen (0.025 ug antibody/well) in a direct binding ELISA.
- immobilized antigen 0.025 ug antibody/well
- the level used in subsequent cELISA's approximately 50% of the plateau activity was reached.
- TM the preferred method, Tween-20 , in the concentration range of about 0.0001-0.1% , preferably a concentration of 0.01%, was routinely used 0.2 ml of assay buffer.
- the competition ELISA data was normalized by using the optical density of wells in which antibody was bound to the solid phase antigen (heptachlor-BSA) in the absence of any competitor as the defined value of 100% activity.
- the test wells, each containing different amounts of competitor, were normalized to the 100% activity wells. Percent inhibition was calculated by subtracting the normalized percent activity from 100.
- Figure 2 shows competition ELISA data for the monoclonal antibody from hybridoma
- Figure 3 shows competition ELISA data for monoclonal antibody from hybridoma Hept-2 when reacted respectively with heptachlor, heptachlor epoxide, aldrin, chlordane, and endrin, as competitors.
- the I 50 values observed for these competitors were all in the range of 1-10 ng/well. Replicate assays generally had less than 10% variation. A smaller I 50 value indicates a greater relative affinity of the antibody for the compound.
- I 50 values were estimated graphically from competition ELISA data.
- Table 1 represents the cross-reactivity of the monoclonal antibody from hybridoma Hept-2 with various cyclic organic compounds including
- Kepone (5) The values listed in Table 1 represent the averages from at least two independent assays. 6. Preparation of Food and Environmental Samples for
- Samples from food or environmental sources are prepared for specific immunoassay by isolation and treatment of the lipid fraction which may contain organic or pesticide materials.
- Assay material from soft samples such as soils, grains and muscle tissue is ground in organic solvent, such as hexane, and subjected to column fractionation.
- organic solvent such as hexane
- the lipid portion of a milk sample is in the low density cream which is assayed for presence of cyclodiene contaminants.
- Meat samples which contain structured fat and epithelial tissue are heated to render any fat.
- samples are heated to 80-150°C for 60 minutes, a temperature of
- a tissue sample is supported by silicanized glass wool during the rendering process.
- the heated samples are dissolved in organic solvent, preferably hexane at a ratio of 0.1 g of rendered fat in the sample to 1 ml of hexane.
- hexane solubilized fat of any meat, soft tissue or milk sample is applied to a previously washed 5-10 gm florisil (Baker or
- the volume of the florisil column is at least ten times the volume of the hexane-fat mixture. In the preferred mode, at least 20 ml of hexane is used to elute the florisil column.
- the sample eluate is dried under a stream of inert gas at room temperature, preferably N Document at 30°C.
- the florisil column used for sample clean-up is prepared by activiation of the gel to remove water and deactivated by addition of a defined amount of water back to the silica gel. In the preferred mode, the florisil is activated by heating, at 650 C overnight, and then stored at 130°C in an open container.
- the resin is selectively deactivated by addition of water back to the dessicated resin by addition with an atomizer with shaking between water additions.
- the preferred deactivated resin contains 7% w/w water. The deactivated resin is allowed to sit overnight before use, and can be stored in a closed container at room temperature.
- Antibodies produced by the above method may be used in a testing screen to identify the presence of cyclodienes in foods or environmental samples when prepared by the above method.
- the antibodies described can be used to distinguish the presence of the most commonly known cyclodiene insecticides.
- Heptachlor was detected in heptachlor-spiked fish muscle and in heptachlor-spiked samples of cream which are extracted with hexane, bound to and extracted from a florisil column with hexane, when the samples were assayed with monoclonal antibody from hybridoma Hept-2.
- Monocloal antibodies have considerable usefulness as diagnostic agents and as binding agents for removal of stable cyclodiene insecticides. TABLE 1
- heptachlor 100 heptachlor epoxide 100 chlordane 75 aldrin 100 endrin 150 dieldrin 300
- Endosulfan (mix) 173 a-Endosulfan 43 b-Endosulfan 250
- a value of 0 indicates that the cross reactivity was less than 0.06%
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PCT/US1991/000151 WO1992012427A1 (fr) | 1991-01-08 | 1991-01-08 | Anticorps monoclonaux destines a des insecticides au cyclodiene et procede de detection desdits insecticides |
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US6635434B1 (en) | 1999-09-17 | 2003-10-21 | Exiqon A/S | Immunoassay for pesticides and their degradation products |
WO2003033537A1 (fr) * | 2001-10-17 | 2003-04-24 | Council Of Scientific And Industrial Research | Procede relatif a l'elaboration d'anticorps a base de jaune d'oeuf pour pesticides organochlores |
CN111856000B (zh) * | 2020-06-04 | 2023-07-07 | 北京勤邦科技股份有限公司 | 一种检测氯丹的试纸条及方法 |
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EP0242589A2 (fr) * | 1986-03-18 | 1987-10-28 | Research Corporation | Détection d'haptènes dans des techniques d'immunoessai |
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EP0242589A2 (fr) * | 1986-03-18 | 1987-10-28 | Research Corporation | Détection d'haptènes dans des techniques d'immunoessai |
Non-Patent Citations (3)
Title |
---|
ACS SYMPOSIUM SERIES.IMMUNOASSAYS FOR TRACE CHEMICAL ANALYSIS.MONITORING TOXIC CHEMICALS IN HUMANS,FOOD,AND THE ENVIROMENT, vol.451, 1990, WASHINGTON D.C.,USA pages 108 - 123 STANKER ET AL 'ANALYSIS OF HEPTACHLOR AND RELATED CYCLODIENE INSECTICIDES IN FOOD PRODUCTS' & DEVELOPED FROM A SYMPOSIUM SPONSORED BY THE INTERNATIONAL CHEMICAL CONGRESS OF PACIFIC BASIN SOCIETEIES, December 1989, HONOLULU,HAWAII * |
See also references of WO9212427A1 * |
U.S.ENVIRON.PROT.AGENCY,RES.DEV.,(REP.) EPA 1988, EPA/600/D-89/189,FIELD SCREENING METHODS HAZARD. WASTE SITE INVEST., 1988 pages 433 - 437 BUSHWAY ET AL 'DETERMINATION OF CHLORDANE IN SOIL BY ENZYME IMMUNOASSAY' * |
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WO1992012427A1 (fr) | 1992-07-23 |
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