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. 1986 May 1;102(5):1826–1831. doi: 10.1083/jcb.102.5.1826

Lateral regionalization and diffusion of a maturation-dependent antigen in the ram sperm plasma membrane

PMCID: PMC2114211  PMID: 3700476

Abstract

We have used a monoclonal antibody ESA 152 in fluorescence recovery after photobleaching (FPR) studies of a maturation-dependent surface antigen of ram sperm. The antibody is an immunoglobulin G secreted by a hybridoma derived from NS1 mouse myeloma cells. The ESA 152 antigen is not detectable in testicular sperm. It is localized on the surface of ejaculated sperm where it is present on all regions of the surface, but tends to be concentrated on the posterior region of the head. The ESA 152 antigen can be extracted by detergents or chloroform-methanol. The extracted antigen is sensitive to proteases and migrates with an apparent Mr approximately 30,000 in SDS-containing 10-20% polyacrylamide gradient gels. FPR measurements of ESA 152 lateral mobility in the membrane yield diffusion coefficients in the range 10(- 9)-10(-8) cm2/s, values typical of lipids but observed for proteins only at the fluid dynamic limit where diffusion is controlled by lipid fluidity. Immobile fractions, typical of membrane proteins, are observed on all regions. When the antigen is stained by a fluoresceinated Fab fragment of the ESA 152 antibody, the diffusibility is highly regionalized, with particularly low, but rapid, recovery on the midpiece. Cross-linking of the antigen with the intact ESA 152 antibody induces a redistribution in which the antigen is excluded from the posterior head region. This cross-linking is accompanied by increases in ESA 152 diffusibility on both the anterior head and the midpiece.

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Selected References

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  1. Axelrod D., Koppel D. E., Schlessinger J., Elson E., Webb W. W. Mobility measurement by analysis of fluorescence photobleaching recovery kinetics. Biophys J. 1976 Sep;16(9):1055–1069. doi: 10.1016/S0006-3495(76)85755-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Axelrod D., Ravdin P., Koppel D. E., Schlessinger J., Webb W. W., Elson E. L., Podleski T. R. Lateral motion of fluorescently labeled acetylcholine receptors in membranes of developing muscle fibers. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4594–4598. doi: 10.1073/pnas.73.12.4594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
  4. Barisas B. G., Leuther M. D. Fluorescence photobleaching recovery measurement of protein absolute diffusion constants. Biophys Chem. 1979 Sep;10(2):221–229. doi: 10.1016/0301-4622(79)85044-9. [DOI] [PubMed] [Google Scholar]
  5. Bearer E. L., Friend D. S. Modifications of anionic-lipid domains preceding membrane fusion in guinea pig sperm. J Cell Biol. 1982 Mar;92(3):604–615. doi: 10.1083/jcb.92.3.604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bradley M. P., Rayns D. G., Forrester I. T. Effects of filipin, digitonin, and polymyxin b on plasma membrane of ram spermatozoa--an EM study. Arch Androl. 1980 May;4(3):195–204. doi: 10.3109/01485018008986963. [DOI] [PubMed] [Google Scholar]
  7. Cherry R. J. Rotational and lateral diffusion of membrane proteins. Biochim Biophys Acta. 1979 Dec 20;559(4):289–327. doi: 10.1016/0304-4157(79)90009-1. [DOI] [PubMed] [Google Scholar]
  8. Dacheux J. L., Voglmayr J. K. Sequence of sperm cell surface differentiation and its relationship to exogenous fluid proteins in the ram epididymis. Biol Reprod. 1983 Nov;29(4):1033–1046. doi: 10.1095/biolreprod29.4.1033. [DOI] [PubMed] [Google Scholar]
  9. Dragsten P., Henkart P., Blumenthal R., Weinstein J., Schlessinger J. Lateral diffusion of surface immunoglobulin, Thy-1 antigen, and a lipid probe in lymphocyte plasma membranes. Proc Natl Acad Sci U S A. 1979 Oct;76(10):5163–5167. doi: 10.1073/pnas.76.10.5163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Frye L. D., Edidin M. The rapid intermixing of cell surface antigens after formation of mouse-human heterokaryons. J Cell Sci. 1970 Sep;7(2):319–335. doi: 10.1242/jcs.7.2.319. [DOI] [PubMed] [Google Scholar]
  11. Galfre G., Howe S. C., Milstein C., Butcher G. W., Howard J. C. Antibodies to major histocompatibility antigens produced by hybrid cell lines. Nature. 1977 Apr 7;266(5602):550–552. doi: 10.1038/266550a0. [DOI] [PubMed] [Google Scholar]
  12. Hammerstedt R. H., Hay S. R., Amann R. P. Modification of ram sperm membranes during epididymal transit. Biol Reprod. 1982 Oct;27(3):745–754. doi: 10.1095/biolreprod27.3.745. [DOI] [PubMed] [Google Scholar]
  13. Holt W. V. Membrane heterogeneity in the mammalian spermatozoon. Int Rev Cytol. 1984;87:159–194. doi: 10.1016/s0074-7696(08)62442-0. [DOI] [PubMed] [Google Scholar]
  14. King S. M., Otter T., Witman G. B. Characterization of monoclonal antibodies against Chlamydomonas flagellar dyneins by high-resolution protein blotting. Proc Natl Acad Sci U S A. 1985 Jul;82(14):4717–4721. doi: 10.1073/pnas.82.14.4717. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Klausner R. D., Wolf D. E. Selectivity of fluorescent lipid analogues for lipid domains. Biochemistry. 1980 Dec 23;19(26):6199–6203. doi: 10.1021/bi00567a039. [DOI] [PubMed] [Google Scholar]
  16. Koehler J. K. The mammalian sperm surface: studies with specific labeling techniques. Int Rev Cytol. 1978;54:73–108. doi: 10.1016/s0074-7696(08)60165-5. [DOI] [PubMed] [Google Scholar]
  17. Koppel D. E., Axelrod D., Schlessinger J., Elson E. L., Webb W. W. Dynamics of fluorescence marker concentration as a probe of mobility. Biophys J. 1976 Nov;16(11):1315–1329. doi: 10.1016/S0006-3495(76)85776-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Koppel D. E. Fluorescence redistribution after photobleaching. A new multipoint analysis of membrane translational dynamics. Biophys J. 1979 Nov;28(2):281–291. doi: 10.1016/S0006-3495(79)85176-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Köhler G., Howe S. C., Milstein C. Fusion between immunoglobulin-secreting and nonsecreting myeloma cell lines. Eur J Immunol. 1976 Apr;6(4):292–295. doi: 10.1002/eji.1830060411. [DOI] [PubMed] [Google Scholar]
  20. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  21. McNutt N. S., Weinstein R. S. Membrane ultrastructure at mammalian intercellular junctions. Prog Biophys Mol Biol. 1973;26:45–101. doi: 10.1016/0079-6107(73)90017-5. [DOI] [PubMed] [Google Scholar]
  22. Myles D. G., Primakoff P., Koppel D. E. A localized surface protein of guinea pig sperm exhibits free diffusion in its domain. J Cell Biol. 1984 May;98(5):1905–1909. doi: 10.1083/jcb.98.5.1905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Nicolson G. L., Yanagimachi R. Mobility and the restriction of mobility of plasma membrane lectin-binding components. Science. 1974 Jun 21;184(4143):1294–1296. doi: 10.1126/science.184.4143.1294. [DOI] [PubMed] [Google Scholar]
  24. Peters R. Translational diffusion in the plasma membrane of single cells as studied by fluorescence microphotolysis. Cell Biol Int Rep. 1981 Aug;5(8):733–760. doi: 10.1016/0309-1651(81)90231-9. [DOI] [PubMed] [Google Scholar]
  25. Saffman P. G., Delbrück M. Brownian motion in biological membranes. Proc Natl Acad Sci U S A. 1975 Aug;72(8):3111–3113. doi: 10.1073/pnas.72.8.3111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Schlegel R. A., Phelps B. M., Waggoner A., Terada L., Williamson P. Binding of merocyanine 540 to normal and leukemic erythroid cells. Cell. 1980 Jun;20(2):321–328. doi: 10.1016/0092-8674(80)90618-2. [DOI] [PubMed] [Google Scholar]
  27. Schmell E. D., Gulyas B. J., Yuan L. C., August J. T. Identification of mammalian sperm surface antigens: II. Characterization of an acrosomal cap protein and a tail protein using monoclonal anti-mouse sperm antibodies. J Reprod Immunol. 1982 May;4(2):91–106. doi: 10.1016/0165-0378(82)90040-7. [DOI] [PubMed] [Google Scholar]
  28. Schmell E. D., Yuan L. C., Gulyas B. J., August J. T. Identification of mammalian sperm surface antigens. I. Production of monoclonal anti-mouse sperm antibodies. Fertil Steril. 1982 Feb;37(2):249–257. [PubMed] [Google Scholar]
  29. Schreiner G. F., Unanue E. R. Membrane and cytoplasmic changes in B lymphocytes induced by ligand-surface immunoglobulin interaction. Adv Immunol. 1976;24:37–165. doi: 10.1016/s0065-2776(08)60329-6. [DOI] [PubMed] [Google Scholar]
  30. Sharon J., Morrison S. L., Kabat E. A. Detection of specific hybridoma clones by replica immunoadsorption of their secreted antibodies. Proc Natl Acad Sci U S A. 1979 Mar;76(3):1420–1424. doi: 10.1073/pnas.76.3.1420. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Staehelin L. A. Structure and function of intercellular junctions. Int Rev Cytol. 1974;39:191–283. doi: 10.1016/s0074-7696(08)60940-7. [DOI] [PubMed] [Google Scholar]
  32. Tank D. W., Wu E. S., Webb W. W. Enhanced molecular diffusibility in muscle membrane blebs: release of lateral constraints. J Cell Biol. 1982 Jan;92(1):207–212. doi: 10.1083/jcb.92.1.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Voglmayr J. K., Fairbanks G., Jackowitz M. A., Colella J. R. Post-testicular developmental changes in the ram sperm cell surface and their relationship to luminal fluid proteins of the reproductive tract. Biol Reprod. 1980 Apr;22(3):655–667. doi: 10.1093/biolreprod/22.3.655. [DOI] [PubMed] [Google Scholar]
  34. Voglmayr J. K., Musto N. A., Saksena S. K., Brown-Woodman D. C., Marley P. B., White I. G. Characteristics of semen collected from the cauda epididymis of conscious rams. J Reprod Fertil. 1977 Mar;49(2):245–251. doi: 10.1530/jrf.0.0490245. [DOI] [PubMed] [Google Scholar]
  35. Voglmayr J. K., Scott T. W., Setchell B. P., Waites G. M. Metabolism of testicular spermatozoa and characteristics of testicular fluid collected from conscious rams. J Reprod Fertil. 1967 Aug;14(1):87–99. doi: 10.1530/jrf.0.0140087. [DOI] [PubMed] [Google Scholar]
  36. Wolf D. E., Edidin M., Handyside A. H. Changes in the organization of the mouse egg plasma membrane upon fertilization and first cleavage: indications from the lateral diffusion rates of fluorescent lipid analogs. Dev Biol. 1981 Jul 15;85(1):195–198. doi: 10.1016/0012-1606(81)90250-5. [DOI] [PubMed] [Google Scholar]
  37. Wolf D. E., Henkart P., Webb W. W. Diffusion, patching, and capping of stearoylated dextrans on 3T3 cell plasma membranes. Biochemistry. 1980 Aug 19;19(17):3893–3904. doi: 10.1021/bi00558a002. [DOI] [PubMed] [Google Scholar]
  38. Wolf D. E., Kinsey W., Lennarz W., Edidin M. Changes in the organization of the sea urchin egg plasma membrane upon fertilization: indications from the lateral diffusion rates of lipid-soluble fluorescent dyes. Dev Biol. 1981 Jan 15;81(1):133–138. doi: 10.1016/0012-1606(81)90355-9. [DOI] [PubMed] [Google Scholar]
  39. Wolf D. E., Schlessinger J., Elson E. L., Webb W. W., Blumenthal R., Henkart P. Diffusion and patching of macromolecules on planar lipid bilayer membranes. Biochemistry. 1977 Jul 26;16(15):3476–3483. doi: 10.1021/bi00634a029. [DOI] [PubMed] [Google Scholar]
  40. Wolf D. E., Voglmayr J. K. Diffusion and regionalization in membranes of maturing ram spermatozoa. J Cell Biol. 1984 May;98(5):1678–1684. doi: 10.1083/jcb.98.5.1678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Wolf D. E., Ziomek C. A. Regionalization and lateral diffusion of membrane proteins in unfertilized and fertilized mouse eggs. J Cell Biol. 1983 Jun;96(6):1786–1790. doi: 10.1083/jcb.96.6.1786. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Wu E. S., Tank D. W., Webb W. W. Unconstrained lateral diffusion of concanavalin A receptors on bulbous lymphocytes. Proc Natl Acad Sci U S A. 1982 Aug;79(16):4962–4966. doi: 10.1073/pnas.79.16.4962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. de StGroth S. F., Scheidegger D. Production of monoclonal antibodies: strategy and tactics. J Immunol Methods. 1980;35(1-2):1–21. doi: 10.1016/0022-1759(80)90146-5. [DOI] [PubMed] [Google Scholar]

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