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Using alanine mutagenesis and hACE2 competition, we found that the RBD mAbs largely fell into two competition groups, one group that blocked hACE2 binding (Group A), and another that minimally inhibited hACE2 binding but instead targeted a cryptic, but conserved, epitope spanning across class III and V epitopes (Group B)

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Furthermore, protein binding, tissue distribution, metabolic conjugation, and elimination kinetics further influence biologically active free drug levels