Methods for selecting low frequency antigen-specific single B lymphocytes
First Claim
1. Two different sets of antigen probes suitable for labelling B lymphocytes, the first set of antigen probes comprising an antigen which binds the antibodies on the surface of particular B lymphocytes, said antigen conjugated with a first cross-linker to a first fluorochrome, and the second set of antigen probes comprising the antigen which is conjugated with a second cross-linker to a second fluorochrome, and wherein the first and second cross-linkers are different and the first and second fluorochrome yield different colors upon activation.
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Abstract
Disclosed are immunofluorescence staining methods which increase the likelihood that antibodies expressed by a single B cell selected and sorted by fluorescence activated cell sorting are specific for the antigen of interest, and which also allow selection of B cells expressing antibodies of high affinity for the antigen of interest. The selection for B cells expressing antibodies to specific antigens is increased by labeling B cells with at least two antigen probes, where each antigen probe includes the antigen of interest and the difference between the two probes is that each is labeled with a different fluorochrome. The specificity of sorting of the desired B cells can be further enhanced by staining those antigen-specific B cells which produce the immunoglobulin isotype (typically IgG), with targeting molecules reactive with B cell markers, such as γ chain and CD19, that are conjugated with different fluorochromes. Thus, the antigen-specific IgG-producing B cells of interest may be labeled with these unique reagents in three or four color FACS, which can sort the desired antigen-specific B cells at enhanced proportions. The differences in relative intensities between the antigen labels and the isotype labels (e.g., IgG labels) among the different antibodies of the single cells selected can be used to determine the relative antigen binding affinity of those antibodies. For example, the ratio of antigen label to IgG label can be calculated for each labeled B cell. The higher the ratio, the higher the relative affinity of the antibodies on the B cells for the antigen. After sorting the B cells with FACS, those B cells with high affinity are preferred for analysis by the single cell-PCR procedure to amplify and clone the VH and VL segments of interest.
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Citations
12 Claims
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1. Two different sets of antigen probes suitable for labelling B lymphocytes, the first set of antigen probes comprising an antigen which binds the antibodies on the surface of particular B lymphocytes, said antigen conjugated with a first cross-linker to a first fluorochrome, and the second set of antigen probes comprising the antigen which is conjugated with a second cross-linker to a second fluorochrome, and wherein the first and second cross-linkers are different and the first and second fluorochrome yield different colors upon activation.
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2. A method of selecting antigen-specific B lymphocytes from a population of B lymphocytes, comprising:
- labeling the B lymphocytes with at least two different antigen probes, wherein the antigen probes comprises the same antigen which binds the antibodies on the target B lymphocyte surface and which is conjugated, through different cross-linkers, with different fluorochrome which yield different colors;
sorting the labeled B lymphocytes by fluorescence activated cell sorting to separate individual B lymphocytes which are labeled with at least two different fluorochromes. - View Dependent Claims (3, 4, 5, 6, 7, 8, 9)
- labeling the B lymphocytes with at least two different antigen probes, wherein the antigen probes comprises the same antigen which binds the antibodies on the target B lymphocyte surface and which is conjugated, through different cross-linkers, with different fluorochrome which yield different colors;
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10. A method of selecting antigen-specific B lymphocytes from a population of B lymphocytes, comprising:
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labeling the B lymphocytes with at least two different antigen probes, wherein the antigen probes comprise the same antigen which binds the antibodies on the target B lymphocyte surface, and the antigen is conjugated with different fluorochromes which yield different colors; labeling the B lymphocytes with a targeting molecule specific for a marker unique to B lymphocytes, wherein the targeting molecule is labeled with a fluorochrome yielding a color different from those used to label the antigen probes; sorting the labeled B lymphocytes by fluorescence activated cell sorting to separate individual B lymphocytes; determining the ratio of the quality of the fluorochrome associated with the antigen probes over the quantity of fluorochrome associated with the B lymhocyte marker; and noting those B lymphocytes with the highest said ratio. - View Dependent Claims (11, 12)
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Specification