Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1983 Jan 1;96(1):68–75. doi: 10.1083/jcb.96.1.68

Reconstitution of ciliary membranes containing tubulin

PMCID: PMC2112241  PMID: 6826653

Abstract

Membranes from the gill cilia of the mollusc Aequipecten irradians may be solubilized readily with Nonidet P-40. When the detergent is removed from the solution by adsorption to polystyrene beads, the proteins of the extract remain soluble. However, when the solution is frozen and thawed, nearly all of the proteins reassociate to form membrane vesicles, recruiting lipids from the medium. The membranes equilibrate as a narrow band (d = 1.167 g/cm3) upon sucrose density gradient centrifugation. The lipid composition of reconstituted membranes (1:2 cholesterol:phospholipids) closely resembles that of the original extract, as does the protein content (45%). Ciliary calmodulin is the major extract protein that does not associate with the reconstituted membrane, even in the presence of 1 mM calcium ions, suggesting that it is a soluble matrix component. The major protein of reconstituted vesicles is membrane tubulin, shown previously to differ hydrophobically from axonemal tubulin. The tubulin is tightly associated with the membrane since extraction with 1 mM iodide or thiocyanate leaves a vesicle fraction whose protein composition and bouyant density are unchanged. Subjecting the detergent-free membrane extract to a freeze-thaw cycle in the presence of elasmobranch brain tubulin or forming membranes by warming the extract in the presence of polymerization-competent tubulin yields a membrane fraction with little incorporated brain tubulin. This suggests that ciliary membrane tubulin specifically associates with lipids, whereas brain tubulin preferentially forms microtubules.

Full Text

The Full Text of this article is available as a PDF (2.8 MB).

Selected References

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

  1. Adoutte A., Ramanathan R., Lewis R. M., Dute R. R., Ling K. Y., Kung C., Nelson D. L. Biochemical studies of the excitable membrane of Paramecium tetraurelia. III. Proteins of cilia and ciliary membranes. J Cell Biol. 1980 Mar;84(3):717–738. doi: 10.1083/jcb.84.3.717. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bhattacharyya B., Volff J. Membrane-bound tubulin in brain and thyroid tissue. J Biol Chem. 1975 Oct 10;250(19):7639–7646. [PubMed] [Google Scholar]
  3. Bhattacharyya B., Wolff J. Polymerisation of membrane tubulin. Nature. 1976 Dec 9;264(5586):576–577. doi: 10.1038/264576a0. [DOI] [PubMed] [Google Scholar]
  4. Caron J. M., Berlin R. D. Interaction of microtubule proteins with phospholipid vesicles. J Cell Biol. 1979 Jun;81(3):665–671. doi: 10.1083/jcb.81.3.665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dentler W. L. Microtubule-membrane interactions in cilia. I. Isolation and characterization of ciliary membranes from Tetrahymena pyriformis. J Cell Biol. 1980 Feb;84(2):364–380. doi: 10.1083/jcb.84.2.364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dentler W. L., Pratt M. M., Stephens R. E. Microtubule-membrane interactions in cilia. II. Photochemical cross-linking of bridge structures and the identification of a membrane-associated dynein-like ATPase. J Cell Biol. 1980 Feb;84(2):381–403. doi: 10.1083/jcb.84.2.381. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Estridge M. Polypeptides similar to the alpha and beta subunits of tubulin are exposed on the neuronal surface. Nature. 1977 Jul 7;268(5615):60–63. doi: 10.1038/268060a0. [DOI] [PubMed] [Google Scholar]
  8. Fairbanks G., Steck T. L., Wallach D. F. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971 Jun 22;10(13):2606–2617. doi: 10.1021/bi00789a030. [DOI] [PubMed] [Google Scholar]
  9. Feit H., Barondes S. H. Colchicine-binding activity in particulate fractions of mouse brain. J Neurochem. 1970 Sep;17(9):1355–1364. doi: 10.1111/j.1471-4159.1970.tb06870.x. [DOI] [PubMed] [Google Scholar]
  10. Feit H., Shay J. W. The assembly of tubulin into membranes. Biochem Biophys Res Commun. 1980 May 14;94(1):324–331. doi: 10.1016/s0006-291x(80)80224-5. [DOI] [PubMed] [Google Scholar]
  11. Feit H., Shelanski M. L. Is tubulin a glycoprotein? Biochem Biophys Res Commun. 1975 Oct 6;66(3):920–927. doi: 10.1016/0006-291x(75)90728-7. [DOI] [PubMed] [Google Scholar]
  12. Gozes I., Littauer U. Z. The alpha-subunit of tubulin is preferentially associated with brain presynaptic membrnae. FEBS Lett. 1979 Mar 1;99(1):86–90. doi: 10.1016/0014-5793(79)80255-0. [DOI] [PubMed] [Google Scholar]
  13. Holloway P. W. A simple procedure for removal of Triton X-100 from protein samples. Anal Biochem. 1973 May;53(1):304–308. doi: 10.1016/0003-2697(73)90436-3. [DOI] [PubMed] [Google Scholar]
  14. Kumar N., Klausner R. D., Weinstein J. N., Blumenthal R., Flavin M. Interaction of tubulin with phospholipid vesicles. II. Physical changes of the protein. J Biol Chem. 1981 Jun 10;256(11):5886–5889. [PubMed] [Google Scholar]
  15. 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]
  16. Langford G. M. In vitro assembly of dogfish brain tubulin and the induction of coiled ribbon polymers by calcium. Exp Cell Res. 1978 Jan;111(1):139–151. doi: 10.1016/0014-4827(78)90244-6. [DOI] [PubMed] [Google Scholar]
  17. Nath J., Flavin M. A structural difference between cytoplasmic and membrane-bound tubulin of brain. FEBS Lett. 1978 Nov 15;95(2):335–338. doi: 10.1016/0014-5793(78)81024-2. [DOI] [PubMed] [Google Scholar]
  18. O'Farrell P. H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem. 1975 May 25;250(10):4007–4021. [PMC free article] [PubMed] [Google Scholar]
  19. Rubin R. W., Quillen M., Corcoran J. J., Ganapathi R., Krishan A. Tubulin as a major cell surface protein in human lymphoid cells of leukemic origin. Cancer Res. 1982 Apr;42(4):1384–1389. [PubMed] [Google Scholar]
  20. Stephens R. E. Chemical differences distinguish ciliary membrane and axonemal tubulins. Biochemistry. 1981 Aug 4;20(16):4716–4723. doi: 10.1021/bi00519a030. [DOI] [PubMed] [Google Scholar]
  21. Stephens R. E. Equimolar heterodimers in microtubules. J Cell Biol. 1982 Aug;94(2):263–270. doi: 10.1083/jcb.94.2.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Stephens R. E. Major membrane protein differences in cilia and flagella: evidence for a membrane-associated tubulin. Biochemistry. 1977 May 17;16(10):2047–2058. doi: 10.1021/bi00629a001. [DOI] [PubMed] [Google Scholar]
  23. Stommel E. W., Stephens R. E., Masure H. R., Head J. F. Specific localization of scallop gill epithelial calmodulin in cilia. J Cell Biol. 1982 Mar;92(3):622–628. doi: 10.1083/jcb.92.3.622. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES