A new filter assay technique was developed to evaluate spermatozoal binding at 5°C for steroid present at 0.1–5,000 nM. A charcoal-stripping technique was used to reduce the amount of endogenous steroid bound by sperm. Both stripped and non-stripped sperm bound steroids to essentially unsaturable sites. Progesterone was bound with greatest affinity followed by estradiol > dihydrotestosterone > testosterone > androsterone, androstenedione > androstanediol, etiocholanolone. We conclude that very few if any specific, saturable, high affinity steroid-binding sites exist on intact testicular or ejaculated sperm.
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Amann et al. (1976) studied this question.