Abstract
Human histocompatibility antigens HLA-A, HLA-B, and HLA-C are a complex of two noncovalently associated subunits: a heavy chain glycoprotein (alpha) carrying the genetic polymorphism and an invariant light chain, beta 2-microglobulin (beta 2m). Upon incubation of papain-solubilized HLA with radiolabeled urinary beta 2m, the latter is incorporated into HLA, where it substitutes for the preexisting beta 2m that has dissociated from the complex. The association-dissociation equilibrium that governs this beta 2m exchange reaction was investigated and found to be characterized by a long lifetime of the complex (half-life of 80 min at 37 degrees C) and a relatively low Kd (4 nM). The beta 2m exchange was used as the basis of a radioimmunoassay for HLA antigens with radiolabeled beta 2m as a unique label for all HLA specificities. In a similar fashion, radiolabeled beta 2m can be incorporated into HLA at the cell surface. Although the process is slower and less extensive than in solution, it can be used as a means to tag cells with specific probes for HLA antigens.
MeSH Terms
Beta-Globulins/metabolism
Cell Line
Cell Membrane/metabolism
HLA Antigens/analysis
Humans
Kinetics
Macromolecular Substances
Membrane Proteins/metabolism
Protein Binding
Radioimmunoassay
Thermodynamics
beta 2-Microglobulin/metabolism,urine
Chemicals
Beta-Globulins
HLA Antigens
Macromolecular Substances
Membrane Proteins
beta 2-Microglobulin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hyafil F
Strominger J L
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