Abstract

The properties of the membrane of intact, metabolically active, human persmatozoa have been studied by the use of 1-anilino-8-napthalene sulfonate (ANS). By fluorescence microscopy it was found that at neutral pH ANS is bound exclusively to the membrane of the entire sperm with some preferential binding to the midpiece, while at low pH some preferential binding to the aerosome was observed. By spectrofluorimetry, fluorescence was found to be enhanced 48-fold on binding of ANS to the spermatozoal membrane, with a 50-nm shift in the emission spectrum of the bound dye. 2.47 ± 0.02 nmoles of ANS were bound per 10 6 spermatozoa ( K=2.3–10 −5 M ). Scatchard plots indicate that all the binding sites on the spermatozoal membrane have similar binding characteristics with a Z value of 84.8. Energy transfer with an efficiency of 7% was found for recently ejaculated spermatozoa. The fluorescence of bound ANS depends on the pH of the medium and possibly on the metabolic state of the cell, since addition of succinate or fructose produces an enhancement of fluorescence, while addition of glucose results in a decrease of this parameter. These changes are inhibited by the presence of cyanide.

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