Why screen the whole repertoire
The antibody you need may sit in a population that most platforms never reach. Memory B-Cells and plasma cells carry different parts of the immune response, and most screening methods are built to interrogate one or the other. Choosing a single population and not sampling the full response narrows diversity before discovery has even started, and the rarest clones, often the ones with the most useful epitopes, are the first to be lost.
Binding is only half the question. A binder that cannot block, agonise, or internalise adds little to a programme if function is the critical parameter. Single B-Cell screening lets us ask the functional question early, at the B-Cell stage, before resource goes into candidates that were never going to advance.
Three things this protects against:
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