Decreased in vitro fertilization efficiencies in the presence of specific cyritestin peptides

Abstract
Synthetic peptides corresponding to specific regions of the mouse acrosomal transmembrane protein cyritestin have been used as competitors in in vitro fertilization experiments. One peptide representing a putative egg‐receptor binding site within the disintegrin domain of cyritestin lowered the fertilization rate to 30% of the normal value.