US5164311A
Expired / Lapsed
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Preparation of an antibody-enzyme conjugate
Assignee: Beckman Coulter Inc
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Filing: 1992-03-19
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Granted: 1992-11-17
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Expires: 2012-03-19
Abstract
Abstract An antibody-enzyme conjugate is prepared having an enzyme to antibody ratio of approximately 3. The conjugate is produced by adding sulfhydryl groups to an antibody and maleimidyl groups to an enzyme to produce a modified antibody and enzyme, and reacting the modified antibody and enzyme to produce the conjugate. In producing the modified antibody and enzyme, about a 15 molar excess of reagents for introducing sulfhydryl and maleimidyl groups is used. When reacting the modified antibody and enzyme, a four molar excess of the modified enzyme is used, and reacting is stopped after a specified period of time by addition of selective reagents. The selective reagents may be cysteine and iodoacetamide.
Inventors
- 👤 Ravinder K. Gupta
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-09 05:05
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/53; G01N33/531; G01N33/532; G01N33/535; Y; Y10; Y10S; Y10S435/00; Y10S435/964; Y10S435/972
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
201 words
A method for producing an enzyme-antibody conjugate of molar ratio of about 3:1, said method comprising: (a) reacting an enzyme with about a 15 molar excess of a reagent capable of introducing maleimidyl groups into said enzyme, said reaction being carried out in a phosphate buffer solution of about pH 7.4 for a period of time of about 1 hour at a temperature of about 21°-25° C.; (b) reacting an antibody with about a 15 mole excess of a reagent capable of introducing sulfhydryl groups into said antibody, said reaction being carried out in a phosphate buffer solution of about pH 7.4 for a period of time of about 1 hour at a temperature of about 22° C.; (c) reacting the products of steps (a) and (b) in a selected proportion such that there is a four molar excess of (a) over (b), said reaction being carried out for a period of time of about 2 hours at a temperature of about 22° C.; (d) stopping the reaction of step (c) by the addition of selective reagents; and (e) concentrating the product of step (d) and purifying the same to thereby obtain said enzyme-antibody conjugate of said ratio molar about 3:1.
Claim 2
Independent Claim
201 words
A method for producing an enzyme-antibody conjugate of molar ratio of about 3:1, said method comprising: (a) reacting an enzyme with about a 15 molar excess of a reagent capable of introducing maleimidyl groups into said enzyme, said reaction being carried out in a phosphate buffer solution of about pH 7.4 for a period of time of about 1 hour at a temperature of about 21°-25° C.; (b) reacting an antibody with about a 15 mole excess of a reagent capable of introducing sulfhydryl groups into said antibody, said reaction being carried out in a phosphate buffer solution of about pH 7.4 for a period of time of about 1 hour at a temperature of about 22° C.; (c) reacting the products of steps (a) and (b) in a selected proportion such that there is a four molar excess of (a) over (b), said reaction being carried out for a period of time of about 2 hours at a temperature of about 22° C.; (d) stopping the reaction of step (c) by the addition of selective reagents; and (e) concentrating the product of step (d) and purifying the same to thereby obtain said enzyme-antibody conjugate of said ratio molar about 3:1.
Claim 3
Dependent Claim
13 words
The method according to claim 1 wherein the antibody is a polyclonal antibody.
Claim 4
Dependent Claim
13 words
The method according to claim 1 wherein the antibody is a monoclonal antibody.
Claim 5
Dependent Claim
13 words
The method according to claim 1 wherein the antibody comprises an antibody fragment.
Claim 6
Dependent Claim
12 words
The method according to claim 1 wherein the enzyme is horseradish peroxidase.
Claim 7
Dependent Claim
13 words
The method of claim 1 wherein said stopping reagents are cysteine and iodoacetamide.
References Cited (Backward Citations)
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