Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1977 Apr 1;73(1):182–192. doi: 10.1083/jcb.73.1.182

Properties of an antiserum against native dynein 1 from sea urchin sperm flagella

PMCID: PMC2109894  PMID: 140174

Abstract

Effects of an antiserum against native dynein 1 from sperm flagella of the sea urchin Strongylocentrotus purpuratus were compared with effects of an antiserum previously obtained against an ATPase-active tryptic fragment (fragment 1A) of dynein 1 from sperm flagella of the sea urchin, Anthocidaris crassispina. Both antisera precipitate dynein 1 and do not precipitate dynein 2. Only the fragment 1A antiserum precipitates fragment 1A and produces a measurable inhibition of dynein 1 ATPase activity. Both antisera inhibit the movement and the movement- coupled ATP dephosphorylation of reactivated spermatozoa. The inhibition of movement by the antiserum against dynein 1 is much less than by the antiserum against fragment 1A, suggesting that a specific interference with the active ATPase site may be required for effective inhibition of movement. Both antisera reduce the bend angle as well as the beat frequency of reactivated S. purpuratus spermatozoa, suggesting that the bend angle may depend on the activity of the dynein arms which generate active sliding.

Full Text

The Full Text of this article is available as a PDF (1.5 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brokaw C. J., Benedict B. Mechanochemical coupling in flagella. I. Movement-dependent dephosphorylation of ATP by glycerinated spermatozoa. Arch Biochem Biophys. 1968 Jun;125(3):770–778. doi: 10.1016/0003-9861(68)90513-4. [DOI] [PubMed] [Google Scholar]
  2. Brokaw C. J. Effects of viscosity and ATP concentration on the movement of reactivated sea-urchin sperm flagella. J Exp Biol. 1975 Jun;62(3):701–719. doi: 10.1242/jeb.62.3.701. [DOI] [PubMed] [Google Scholar]
  3. Gibbons B. H., Gibbons I. R. The effect of partial extraction of dynein arms on the movement of reactivated sea-urchin sperm. J Cell Sci. 1973 Sep;13(2):337–357. doi: 10.1242/jcs.13.2.337. [DOI] [PubMed] [Google Scholar]
  4. Gibbons B. H., Ogawa K., Gibbons I. R. The effect of antidynein 1 serum on the movement of reactivated sea urchin sperm. J Cell Biol. 1976 Dec;71(3):823–831. doi: 10.1083/jcb.71.3.823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gibbons I. R., Fronk E. Some properties of bound and soluble dynein from sea urchin sperm flagella. J Cell Biol. 1972 Aug;54(2):365–381. doi: 10.1083/jcb.54.2.365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ogawa K., Gibbons I. R. Dynein 2. A new adenosine triphosphatase from sea urchin sperm flagella. J Biol Chem. 1976 Sep 25;251(18):5793–5801. [PubMed] [Google Scholar]
  7. Ogawa K., Mohri H. Studies on flagellar ATPase from sea urchin spermatozoa. I. Purification and some properties of the enzyme. Biochim Biophys Acta. 1972 Jan 21;256(1):142–155. doi: 10.1016/0005-2728(72)90169-7. [DOI] [PubMed] [Google Scholar]
  8. Ogawa K. Studies on flagellar ATPase from sea urchin spermatozoa. II. Effect of trypsin digestion on the enzyme. Biochim Biophys Acta. 1973 Feb 15;293(2):514–525. doi: 10.1016/0005-2744(73)90358-6. [DOI] [PubMed] [Google Scholar]
  9. Okuno M., Ogawa K., Mohri H. Inhibition of movement and ATP-ase activity of demembranated sea urchin spermatozoa by anti-dynein antiserum. Biochem Biophys Res Commun. 1976 Feb 9;68(3):901–906. doi: 10.1016/0006-291x(76)91230-4. [DOI] [PubMed] [Google Scholar]
  10. Warner F. D., Satir P. The structural basis of ciliary bend formation. Radial spoke positional changes accompanying microtubule sliding. J Cell Biol. 1974 Oct;63(1):35–63. doi: 10.1083/jcb.63.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES