US 12,693,296 B2 · Method for determining antibody dissociation rate

Abstract

The present invention is directed to a method of measuring the dissociation rate of the binding of an antibody to an antigen. The method has two phases: a first phase of binding and a second phase of dissociation. The first phase of the assay has a probe coated with an antigen, or protein G, or an anti-human IgG Fc antibody. The probe is immersed in a sample solution containing an antibody, followed by a wash sequence, then the probe is transferred to a reagent with a biotinylated antigen. After an incubation, the antibody bound on the probe binds to the biotinylated antigen to form an immune complex. Fluorescent signal is produced by immersing the probe in a reagent having a fluorescent tagged streptavidin. The last step of the first phase is a measurement of fluorescent on the probe tip. The second phase of the assay is making subsequent fluorescent measurements over time to monitor the loss in fluorescence indicating dissociation of the immune complex and calculating the dissociation rate of the binding of the antibody to the antigen.

Claims17

Dependent claims

A method of measuring the dissociation rate of the binding of an antibody to an antigen, comprising the steps of:

(a) obtaining a probe having an antigen immobilized on the tip of the probe, wherein the diameter of the tip surface is ≤5 mm;
(b) dipping the probe tip into an antibody sample solution, wherein the antibody is specifically against the antigen;
(c) dipping the probe tip into an antigen solution comprising the antigen conjugated with biotin;
(d) dipping the probe tip into a signal solution comprising fluorescent labels conjugated to streptavidin, to form an immunocomplex among the antigen immobilized on the probe, the antibody, the biotinylated antigen, and the streptavidin conjugated with fluorescent labels on the probe tip;
(e) dipping the probe tip into a wash solution;
(f) dipping the probe tip in a first aqueous solution and measuring the first fluorescent signal of the immunocomplex emitted at the probe tip;
(g) dipping the probe tip into a second aqueous solution for a period of time and then measuring the second fluorescent signal of the immunocomplex emitted at the probe tip;
(h) repeating step (g) 0 to 30 times, and
(i) determining the dissociation rate of the antibody based on the measured fluorescent signal change between steps (f) and (g) and the length of the period of time in step (g).

6 more elements

A method of measuring the dissociation rate of the binding of an IgG antibody to an antigen of interest, comprising the steps of:

(a) obtaining a probe having protein G, or an anti-IgG Fc antibody immobilized on the tip of the probe, wherein the diameter of the tip surface is ≤5 mm;
(b) dipping the probe tip into an antibody sample solution to capture IgG antibody in the antibody sample solution on the probe, wherein at least a portion of the captured IgG antibody is specifically against the antigen of interest;
(c) dipping the probe tip into a solution comprising the antigen conjugated with biotin;
(d) dipping the probe tip into a signal solution comprising fluorescent labels conjugated to streptavidin, to form an immunocomplex among (i) the protein G or anti-IgG Fc antibody immobilized on the probe, (ii) the IgG antibody against the antigen, (iii) the biotinylated antigen, and (iv) the streptavidin conjugated with fluorescent labels on the probe tip;
(e) dipping the probe tip into a wash solution;
(f) dipping the probe tip in a first aqueous solution and measuring the first fluorescent signal of the immunocomplex emitted at the probe tip;
(g) dipping the probe tip into a second aqueous solution for a period of time and then measuring the second fluorescent signal of the immunocomplex emitted at the probe tip;
(h) repeating step (g) 0 to 30 times, and
(i) determining the dissociation rate of the antibody based on the measured fluorescent signal change between steps (f) and (g) and the length of the period of time in step (g).

6 more elements

Dependencies are inferred from the claim text.

Method for determining antibody dissociation rate

Life of this patent

Method for determining antibody dissociation rate

Life of this patent

Abstract

Claims17