Abstract
Fragmented flagellar axonemes of sand dollar spermatozoa were reactivated by rapid photolysis of caged ATP. After a time lag of 10 ms, axonemes treated with protease started sliding disintegration. Axonemes without protease digestion started nanometer-scale high-frequency oscillation after a similar time lag. Force development in the sliding disintegration was measured with a flexible glass needle and its time course was corresponded well to that of the dynein-ADP intermediate production estimated using kinetic rates previously reported. However, with a high concentration ( approximately 80 microM) of vanadate, which binds to the dynein-ADP intermediate and forms a stable complex of dynein-ADP-vanadate, the time course of force development in sliding disintegration was not affected at all. In the case of high frequency oscillation, the time lag to start the oscillation, the initial amplitude, and the initial frequency were not affected by vanadate, though the oscillation once started was damped more quickly at higher concentrations of vanadate. These results suggest that during the initial turnover of ATP hydrolysis, force generation of dynein is not blocked by vanadate. A vanadate-insensitive dynein-ADP is postulated as a force-generating intermediate.
Full Text
The Full Text of this article is available as a PDF (361.6 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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. Direct measurements of sliding between outer doublet microtubules in swimming sperm flagella. Science. 1989 Mar 24;243(4898):1593–1596. doi: 10.1126/science.2928796. [DOI] [PubMed] [Google Scholar]
- Burgess S. A. Rigor and relaxed outer dynein arms in replicas of cryofixed motile flagella. J Mol Biol. 1995 Jun 30;250(1):52–63. doi: 10.1006/jmbi.1995.0357. [DOI] [PubMed] [Google Scholar]
- Gibbons B. H., Gibbons I. R. Flagellar movement and adenosine triphosphatase activity in sea urchin sperm extracted with triton X-100. J Cell Biol. 1972 Jul;54(1):75–97. doi: 10.1083/jcb.54.1.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons B. H., Gibbons I. R. Properties of flagellar "rigor waves" formed by abrupt removal of adenosine triphosphate from actively swimming sea urchin sperm. J Cell Biol. 1974 Dec;63(3):970–985. doi: 10.1083/jcb.63.3.970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons I. R., Cosson M. P., Evans J. A., Gibbons B. H., Houck B., Martinson K. H., Sale W. S., Tang W. J. Potent inhibition of dynein adenosinetriphosphatase and of the motility of cilia and sperm flagella by vanadate. Proc Natl Acad Sci U S A. 1978 May;75(5):2220–2224. doi: 10.1073/pnas.75.5.2220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons I. R., Evans J. A., Gibbons B. H. Acetate anions stabilize the latency of dynein 1 ATPase and increase the velocity of tubule sliding in reactivated sperm flagella. Prog Clin Biol Res. 1982;80:181–184. doi: 10.1002/cm.970020734. [DOI] [PubMed] [Google Scholar]
- Gibbons I. R., Gibbons B. H., Mocz G., Asai D. J. Multiple nucleotide-binding sites in the sequence of dynein beta heavy chain. Nature. 1991 Aug 15;352(6336):640–643. doi: 10.1038/352640a0. [DOI] [PubMed] [Google Scholar]
- Gibbons I. R. Sliding and bending in sea urchin sperm flagella. Symp Soc Exp Biol. 1982;35:225–287. [PubMed] [Google Scholar]
- Goldman Y. E., Hibberd M. G., McCray J. A., Trentham D. R. Relaxation of muscle fibres by photolysis of caged ATP. Nature. 1982 Dec 23;300(5894):701–705. doi: 10.1038/300701a0. [DOI] [PubMed] [Google Scholar]
- Goodenough U. W., Heuser J. E. Substructure of the outer dynein arm. J Cell Biol. 1982 Dec;95(3):798–815. doi: 10.1083/jcb.95.3.798. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodno C. C., Taylor E. W. Inhibition of actomyosin ATPase by vanadate. Proc Natl Acad Sci U S A. 1982 Jan;79(1):21–25. doi: 10.1073/pnas.79.1.21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hibberd M. G., Dantzig J. A., Trentham D. R., Goldman Y. E. Phosphate release and force generation in skeletal muscle fibers. Science. 1985 Jun 14;228(4705):1317–1319. doi: 10.1126/science.3159090. [DOI] [PubMed] [Google Scholar]
- Higuchi H., Muto E., Inoue Y., Yanagida T. Kinetics of force generation by single kinesin molecules activated by laser photolysis of caged ATP. Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4395–4400. doi: 10.1073/pnas.94.9.4395. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holzbaur E. L., Johnson K. A. ADP release is rate limiting in steady-state turnover by the dynein adenosinetriphosphatase. Biochemistry. 1989 Jun 27;28(13):5577–5585. doi: 10.1021/bi00439a036. [DOI] [PubMed] [Google Scholar]
- Holzbaur E. L., Johnson K. A. Microtubules accelerate ADP release by dynein. Biochemistry. 1989 Aug 22;28(17):7010–7016. doi: 10.1021/bi00443a034. [DOI] [PubMed] [Google Scholar]
- Inaba K., Mohri H. Dynamic conformational changes of 21 S dynein ATPase coupled with ATP hydrolysis revealed by proteolytic digestion. J Biol Chem. 1989 May 15;264(14):8384–8388. [PubMed] [Google Scholar]
- Inaba K., Okuno M., Mohri H. Anthraniloyl ATP, a fluorescent analog of ATP, as a substrate for dynein ATPase and flagellar motility. Arch Biochem Biophys. 1989 Oct;274(1):209–215. doi: 10.1016/0003-9861(89)90432-3. [DOI] [PubMed] [Google Scholar]
- Johnson K. A. The pathway of ATP hydrolysis by dynein. Kinetics of a presteady state phosphate burst. J Biol Chem. 1983 Nov 25;258(22):13825–13832. [PubMed] [Google Scholar]
- Kamimura S., Kamiya R. High-frequency nanometre-scale vibration in 'quiescent' flagellar axonemes. Nature. 1989 Aug 10;340(6233):476–478. doi: 10.1038/340476a0. [DOI] [PubMed] [Google Scholar]
- Kamimura S., Kamiya R. High-frequency vibration in flagellar axonemes with amplitudes reflecting the size of tubulin. J Cell Biol. 1992 Mar;116(6):1443–1454. doi: 10.1083/jcb.116.6.1443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kamimura S., Takahashi K. Direct measurement of the force of microtubule sliding in flagella. Nature. 1981 Oct 15;293(5833):566–568. doi: 10.1038/293566a0. [DOI] [PubMed] [Google Scholar]
- Kaplan J. H., Forbush B., 3rd, Hoffman J. F. Rapid photolytic release of adenosine 5'-triphosphate from a protected analogue: utilization by the Na:K pump of human red blood cell ghosts. Biochemistry. 1978 May 16;17(10):1929–1935. doi: 10.1021/bi00603a020. [DOI] [PubMed] [Google Scholar]
- Lymn R. W., Taylor E. W. Mechanism of adenosine triphosphate hydrolysis by actomyosin. Biochemistry. 1971 Dec 7;10(25):4617–4624. doi: 10.1021/bi00801a004. [DOI] [PubMed] [Google Scholar]
- McCray J. A., Herbette L., Kihara T., Trentham D. R. A new approach to time-resolved studies of ATP-requiring biological systems; laser flash photolysis of caged ATP. Proc Natl Acad Sci U S A. 1980 Dec;77(12):7237–7241. doi: 10.1073/pnas.77.12.7237. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mocz G., Helms M. K., Jameson D. M., Gibbons I. R. Probing the nucleotide binding sites of axonemal dynein with the fluorescent nucleotide analogue 2'(3')-O-(-N-Methylanthraniloyl)-adenosine 5'-triphosphate. Biochemistry. 1998 Jul 7;37(27):9862–9869. doi: 10.1021/bi9730184. [DOI] [PubMed] [Google Scholar]
- Ogawa K. Four ATP-binding sites in the midregion of the beta heavy chain of dynein. Nature. 1991 Aug 15;352(6336):643–645. doi: 10.1038/352643a0. [DOI] [PubMed] [Google Scholar]
- Oiwa K., Takahashi K. The force-velocity relationship for microtubule sliding in demembranated sperm flagella of the sea urchin. Cell Struct Funct. 1988 Jun;13(3):193–205. doi: 10.1247/csf.13.193. [DOI] [PubMed] [Google Scholar]
- Okuno M. Inhibition and relaxation of sea urchin sperm flagella by vanadate. J Cell Biol. 1980 Jun;85(3):712–725. doi: 10.1083/jcb.85.3.712. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Omoto C. K., Johnson K. A. Activation of the dynein adenosinetriphosphatase by microtubules. Biochemistry. 1986 Jan 28;25(2):419–427. doi: 10.1021/bi00350a022. [DOI] [PubMed] [Google Scholar]
- Omoto C. K. Sea urchin axonemal motion supported by fluorescent, ribose-modified analogues of ATP. J Muscle Res Cell Motil. 1992 Dec;13(6):635–639. doi: 10.1007/BF01738253. [DOI] [PubMed] [Google Scholar]
- Porter M. E., Johnson K. A. Transient state kinetic analysis of the ATP-induced dissociation of the dynein-microtubule complex. J Biol Chem. 1983 May 25;258(10):6582–6587. [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]
- Shimizu T., Johnson K. A. Presteady state kinetic analysis of vanadate-induced inhibition of the dynein ATPase. J Biol Chem. 1983 Nov 25;258(22):13833–13840. [PubMed] [Google Scholar]
- Shimizu T., Marchese-Ragona S. P., Johnson K. A. Activation of the dynein adenosinetriphosphatase by cross-linking to microtubules. Biochemistry. 1989 Aug 22;28(17):7016–7021. doi: 10.1021/bi00443a035. [DOI] [PubMed] [Google Scholar]
- Shimizu T. Steady-state kinetic study of vanadate-induced inhibition of ciliary dynein adenosinetriphosphatase activity from Tetrahymena. Biochemistry. 1981 Jul 21;20(15):4347–4354. doi: 10.1021/bi00518a018. [DOI] [PubMed] [Google Scholar]
- Shingyoji C., Takahashi K. Cyclical bending movements induced locally by successive iontophoretic application of ATP to an elastase-treated flagellar axoneme. J Cell Sci. 1995 Apr;108(Pt 4):1359–1369. doi: 10.1242/jcs.108.4.1359. [DOI] [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]
- Takahashi K., Shingyoji C., Kamimura S. Microtubule sliding in reactivated flagella. Symp Soc Exp Biol. 1982;35:159–177. [PubMed] [Google Scholar]
- Tani T., Kamimura S. Reactivation of sea-urchin sperm flagella induced by rapid photolysis of caged ATP. J Exp Biol. 1998 May;201(Pt 10):1493–1503. doi: 10.1242/jeb.201.10.1493. [DOI] [PubMed] [Google Scholar]
- Thirlwell H., Sleep J. A., Ferenczi M. A. Inhibition of unloaded shortening velocity in permeabilized muscle fibres by caged ATP compounds. J Muscle Res Cell Motil. 1995 Apr;16(2):131–137. doi: 10.1007/BF00122531. [DOI] [PubMed] [Google Scholar]
- Tsukita S., Tsukita S., Usukura J., Ishikawa H. ATP-dependent structural changes of the outer dynein arm in Tetrahymena cilia: a freeze-etch replica study. J Cell Biol. 1983 May;96(5):1480–1485. doi: 10.1083/jcb.96.5.1480. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vale R. D., Schnapp B. J., Mitchison T., Steuer E., Reese T. S., Sheetz M. P. Different axoplasmic proteins generate movement in opposite directions along microtubules in vitro. Cell. 1985 Dec;43(3 Pt 2):623–632. doi: 10.1016/0092-8674(85)90234-x. [DOI] [PubMed] [Google Scholar]
- Vale R. D., Soll D. R., Gibbons I. R. One-dimensional diffusion of microtubules bound to flagellar dynein. Cell. 1989 Dec 1;59(5):915–925. doi: 10.1016/0092-8674(89)90614-4. [DOI] [PubMed] [Google Scholar]
- Witman G. B., Minervini N. Dynein arm conformation and mechanochemical transduction in the eukaryotic flagellum. Symp Soc Exp Biol. 1982;35:203–223. [PubMed] [Google Scholar]
- Yagi T., Kamimura S., Kamiya R. Nanometer scale vibration in mutant axonemes of Chlamydomonas. Cell Motil Cytoskeleton. 1994;29(2):177–185. doi: 10.1002/cm.970290209. [DOI] [PubMed] [Google Scholar]
- Yano Y., Miki-Noumura T. Sliding velocity between outer doublet microtubules of sea-urchin sperm axonemes. J Cell Sci. 1980 Aug;44:169–186. doi: 10.1242/jcs.44.1.169. [DOI] [PubMed] [Google Scholar]
