Abstract
Properties of the sliding disintegration response of demembranated tetrahymena cilia have been studied by measuring the spectrophotomeric response or turbidity of cilia suspensions at a wavelength of 350 nm relative to changes in the dynein substrate (MgATP(2-)) concentration. The maximum decrease in turbidity occurs in 20 muM ATP, and 90 percent of the decrease occurs in approximately 5.9 s. At lower ATP concentrations (1-20 muM), both the velocity and magnitude of the turbidity decreases are proportional to ATP concentration. The velocity data for 20 muM ATP permit construction of a reaction velocity curve suggesting that changes in turbidity are directly proportional to the extent and velocity of disintegration. At ATP concentrations more than 20 muM (50muM to 5mM), both velocity and magnitude of the turbidimetric response are reduced by approximately 50 percent. This apparent inhibition results in a biphasic response curve that may be related to activation of residual shear resistance or regulatory components at the higher ATP concentrations. The inhibitory effects of elevated ATP can be eliminated by mild trypsin proteolysis, whereupon the reaction goes to completion at any ATP concentration. The turbidimetric responses of the axoneme-substrate suspensions are consistent with the extent and type of axoneme disintegration revealed by electron microscope examination of the various suspensions, suggesting that the turbidimetric assay may prove to be a reliable means for assessing the state of axoneme integrity.
Full Text
The Full Text of this article is available as a PDF (1.1 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- 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]
- 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]
- Brokaw C. J. Elastase digestion of demembranated sperm flagella. Science. 1980 Mar 21;207(4437):1365–1367. doi: 10.1126/science.6898364. [DOI] [PubMed] [Google Scholar]
- Brokaw C. J., Simonick T. F. Motility of triton-demembranated sea urchin sperm flagella during digestion by trypsin. J Cell Biol. 1977 Dec;75(3):650–665. doi: 10.1083/jcb.75.3.650. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons B. H., Gibbons I. R. Calcium-induced quiescence in reactivated sea urchin sperm. J Cell Biol. 1980 Jan;84(1):13–27. doi: 10.1083/jcb.84.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons I. R. Studies on the adenosine triphosphatase activity of 14 S and 30 S dynein from cilia of Tetrahymena. J Biol Chem. 1966 Dec 10;241(23):5590–5596. [PubMed] [Google Scholar]
- Gordon A. M., Huxley A. F., Julian F. J. The variation in isometric tension with sarcomere length in vertebrate muscle fibres. J Physiol. 1966 May;184(1):170–192. doi: 10.1113/jphysiol.1966.sp007909. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hata H., Yano Y., Miki-Noumura T. ATP concentration dependency of the tubule-extrusion velocity from the axonemes. Exp Cell Res. 1979 Sep;122(2):416–419. doi: 10.1016/0014-4827(79)90322-7. [DOI] [PubMed] [Google Scholar]
- Okuno M., Brokaw C. J. Inhibition of movement of trition-demembranated sea-urchin sperm flagella by Mg2+, ATP4-, ADP and P1. J Cell Sci. 1979 Aug;38:105–123. doi: 10.1242/jcs.38.1.105. [DOI] [PubMed] [Google Scholar]
- Sale W. S., Gibbons I. R. Study of the mechanism of vanadate inhibition of the dynein cross-bridge cycle in sea urchin sperm flagella. J Cell Biol. 1979 Jul;82(1):291–298. doi: 10.1083/jcb.82.1.291. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sale W. S., Satir P. Direction of active sliding of microtubules in Tetrahymena cilia. Proc Natl Acad Sci U S A. 1977 May;74(5):2045–2049. doi: 10.1073/pnas.74.5.2045. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Satir P. Morphological aspects of ciliary motility. J Gen Physiol. 1967 Jul;50(6 Suppl):241–258. doi: 10.1085/jgp.50.6.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Storer A. C., Cornish-Bowden A. Concentration of MgATP2- and other ions in solution. Calculation of the true concentrations of species present in mixtures of associating ions. Biochem J. 1976 Oct 1;159(1):1–5. doi: 10.1042/bj1590001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Summers K. E., Gibbons I. R. Adenosine triphosphate-induced sliding of tubules in trypsin-treated flagella of sea-urchin sperm. Proc Natl Acad Sci U S A. 1971 Dec;68(12):3092–3096. doi: 10.1073/pnas.68.12.3092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warner F. D., Mitchell D. R. Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia. J Cell Biol. 1978 Feb;76(2):261–277. doi: 10.1083/jcb.76.2.261. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Zanetti N. C., Mitchell D. R., Warner F. D. Effects of divalent cations on dynein cross bridging and ciliary microtubule sliding. J Cell Biol. 1979 Mar;80(3):573–588. doi: 10.1083/jcb.80.3.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
