The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Dynamic instability of individual microtubules analyzed by video light microscopy: rate constants and transition frequencies
Open accessAbstract
We have developed video microscopy methods to visualize the assembly and disassembly of individual microtubules at 33-ms intervals. Porcine brain tubulin, free of microtubule-associated proteins, was assembled onto axoneme fragments at 37 degrees C, and the dynamic behavior of the plus and minus ends of microtubules was analyzed for tubulin concentrations between 7 and 15.5 microM. Elongation and rapid shortening were distinctly different phases. At each end, the elongation phase was characterized by a second order association and a substantial first order dissociation reaction. Association rate constants were 8.9 and 4.3 microM-1 s-1 for the plus and minus ends, respectively; and the corresponding dissociation rate constants were 44 and 23 s-1. For both ends, the rate of tubulin dissociation equaled the rate of tubulin association at 5 microM. The rate of rapid shortening was similar at the two ends (plus = 733 s-1; minus = 915 s-1), and did not vary with tubulin concentration. Transitions between phases were abrupt and stochastic. As the tubulin concentration was increased, catastrophe frequency decreased at both ends, and rescue frequency increased dramatically at the minus end. This resulted in fewer rapid shortening phases at higher tubulin concentrations for both ends and shorter rapid shortening phases at the minus end. At each concentration, the frequency of catastrophe was slightly greater at the plus end, and the frequency of rescue was greater at the minus end. Our data demonstrate that microtubules assembled from pure tubulin undergo dynamic instability over a twofold range of tubulin concentrations, and that the dynamic instability of the plus and minus ends of microtubules can be significantly different. Our analysis indicates that this difference could produce treadmilling, and establishes general limits on the effectiveness of length redistribution as a measure of dynamic instability. Our results are consistent with the existence of a GTP cap during elongation, but are not consistent with existing GTP cap models.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“indicating that a higher tubulin concentration and, consequently, a higher MT growth rate have a catastrophe-suppressing effect, in line with previously published data [20]”
From In vitro reconstitution of the functional interplay between MCAK and EB3 at microtubule plus ends (2010) · cites this paper as [20]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Morrissey, J. H. (1981) · Analytical Biochemistry · doi:10.1016/0003-2697(81)90783-1 · Cited by 4,061
Dynamic instability of microtubule growth
Mitchison, T., & Kirschner, M. (1984) · Nature · doi:10.1038/312237a0 · Cited by 3,337
Merril, C. R., Goldman, D. A., Sedman, S. A., & Ebert, M. H. (1981) · Science · doi:10.1126/science.6162199 · Cited by 2,933
An Introduction to Error Analysis
Taylor, J. R. (1982) · Medical Entomology and Zoology · Cited by 2,807
Microtubule assembly nucleated by isolated centrosomes
Mitchison, T. J., & Kirschner, M. W. (1984) · Nature · doi:10.1038/312232a0 · Cited by 779
Head to tail polymerization of actin
Wegner, A. (1976) · Journal of Molecular Biology · doi:10.1016/s0022-2836(76)80100-3 · Cited by 716
Visualization of the dynamic instability of individual microtubules by dark-field microscopy
Horio, T., & Hotani, H. (1986) · Nature · doi:10.1038/321605a0 · Cited by 565
ALLEN, R. D., Allen, N. S., & Travis, J. L. (1981) · Cell Motility · doi:10.1002/cm.970010303 · Cited by 419
Sites of microtubule assembly and disassembly in the mitotic spindle
Mitchison, T. J., Evans, L., Schulze, E., & Kirschner, M. W. (1986) · Cell · doi:10.1016/0092-8674(86)90283-7 · Cited by 415
Gard, D. L., & Kirschner, M. W. (1987) · The Journal of Cell Biology · doi:10.1083/jcb.105.5.2203 · Cited by 354
Microtubule dynamics in interphase cells
Schulze, E., & Kirschner, M. (1986) · The Journal of cell biology · doi:10.1083/jcb.102.3.1020 · Cited by 335
Inoué, S. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.89.2.346 · Cited by 308
Kinetic analysis of guanosine 5'-triphosphate hydrolysis associated with tubulin polymerization
Carlier, M. F., & Pantaloni, D. (1981) · Biochemistry · doi:10.1021/bi00510a030 · Cited by 294
Tubulin-nucleotide interactions during the polymerization and depolymerization of microtubules
Weisenberg, R. C., Deery, W. J., & Dickinson, P. J. (1976) · Biochemistry · doi:10.1021/bi00664a018 · Cited by 289
Bergen, L. G., & Borisy, G. G. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.84.1.141 · Cited by 284
Kinetic analysis of microtubule self-assembly in vitro
Johnson, K. A., & Borisy, G. G. (1977) · Journal of Molecular Biology · doi:10.1016/0022-2836(77)90020-1 · Cited by 266
The kinetics of microtubule assembly. Evidence for a two-stage nucleation mechanism.
Voter, W. A., & Erickson, H. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)90982-8 · Cited by 184
Self-citationGuanosinetriphosphatase activity of tubulin associated with microtubule assembly.
David-Pfeuty, T., Erickson, H., & Pantaloni, D. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.12.5372 · Cited by 182
Self-citationDynamic instability of microtubules
Cassimeris, L., Walker, R. A., Pryer, N., & Salmon, E. D. (1987) · BioEssays · doi:10.1002/bies.950070403 · Cited by 171
Self-citationNucleotide binding and phosphorylation in microtubule assembly in vitro
Penningroth, S. M., & Kirschner, M. W. (1977) · Journal of Molecular Biology · doi:10.1016/0022-2836(77)90108-5 · Cited by 163
Interference of GTP hydrolysis in the mechanism of microtubule assembly: an experimental study.
Carlier, M. F., Hill, T. L., & Chen, Y. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.3.771 · Cited by 162
Direct observation of steady-state microtubule dynamics.
Kristofferson, D., Mitchison, T. J., & Kirschner, M. W. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.102.3.1007 · Cited by 136
Electron microscopy of map 2 (microtubule-associated protein 2)
Voter, W. A., & Erickson, H. (1982) · Journal of Ultrastructure Research · doi:10.1016/s0022-5320(82)80051-8 · Cited by 135
Self-citationKirschner, M. W., & Mitchison, T. J. (1986) · Nature · doi:10.1038/324621a0 · Cited by 123
Microtubule dynamics in vivo: a test of mechanisms of turnover.
Sammak, P. J., Gorbsky, G. J., & Borisy, G. G. (1987) · The Journal of Cell Biology · doi:10.1083/jcb.104.3.395 · Cited by 119
Dynamics of microtubule depolymerization in monocytes.
Cassimeris, L., Wadsworth, P., & Salmon, E. D. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.102.6.2023 · Cited by 118
Self-citationGTP hydrolysis during microtubule assembly
O’Brien, E. T., Voter, W. A., & Erickson, H. (1987) · Biochemistry · doi:10.1021/bi00387a061 · Cited by 116
Self-citationMonte Carlo study of the GTP cap in a five-start helix model of a microtubule.
Chen, Y. D., & Hill, T. L. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.4.1131 · Cited by 111
Wadsworth, P., & Salmon, E. D. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.102.3.1032 · Cited by 106
Self-citationPhase dynamics at microtubule ends: the coexistence of microtubule length changes and treadmilling
Farrell, K., Jordan, M. A., Miller, H., & Wilson, L. (1987) · The Journal of Cell Biology · doi:10.1083/jcb.104.4.1035 · Cited by 101
Phase changes at the end of a microtubule with a GTP cap.
Hill, T. L., & Chen, Y. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.18.5772 · Cited by 97
Carlier, M. F., Didry, D., & Pantaloni, D. (1987) · Biochemistry · doi:10.1021/bi00388a036 · Cited by 94
Chapter 23 Preparation and Purification of Dynein
Bell, C. W., Fraser, C. F., Sale, W. S., Tang, W.-J. Y., & Gibbons, I. R. (1982) · Methods in cell biology · doi:10.1016/s0091-679x(08)60666-4 · Cited by 83
[53] Viewing single microtubules by video light microscopy
Schnapp, B. J. (1986) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(86)34121-1 · Cited by 75
Assembly properties of fluorescein-labeled tubulin in vitro before and after fluorescence bleaching.
Leslie, R. J., Saxton, W. M., Mitchison, T. J., Neighbors, B., Salmon, E. D., & McIntosh, J. R. (1984) · The Journal of Cell Biology · doi:10.1083/jcb.99.6.2146 · Cited by 59
Self-citationYANAGISAWA, T., Hasegawa, S., & Mohri, H. (1968) · Experimental Cell Research · doi:10.1016/0014-4827(68)90549-1 · Cited by 53
Participation of guanine nucleotides in nucleation and elongation steps of microtubule assembly.
Karr, T. L., Podrasky, A. E., & Purich, D. L. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.11.5475 · Cited by 53
Pryer, N., Wadsworth, P., & Salmon, E. D. (1986) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970060602 · Cited by 42
Self-citationChapter 6 Techniques for Observing Living Gametes and Embryos
Lutz, D. A., & Inoué, S. (1986) · Methods in cell biology · doi:10.1016/s0091-679x(08)60344-1 · Cited by 38
Dephosphorylation of Tubulin-bound Guanosine Triphosphate during Microtubule Assembly
Kobayashi, T. (1975) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a130834 · Cited by 33
Directed elongation model for microtubule GTP hydrolysis.
Caplow, M., & Reid, R. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.10.3267 · Cited by 31
An isoenergetic exchange mechanism which accounts for tubulin-GDP stabilization of microtubules.
Zeebèrg, B. R., & Caplow, M. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43232-2 · Cited by 18
[49] Preparation and characterization of fluorescent analogs of tubulin
Wadsworth, P., & Salmon, E. D. (1986) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(86)34117-x · Cited by 13
Self-citationBorisy, G. G., & Bergen, L. G. (1982) · Methods in cell biology · doi:10.1016/s0091-679x(08)60654-8 · Cited by 10
Location of the Guanosine Triphosphate (GTP) Hydrolysis Site in Microtubulesa
Caplow, M. (1986) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1986.tb38428.x · Cited by 5
Flagged first, then by citations
Cited by
Sorted by citations
Electrostatics of nanosystems: Application to microtubules and the ribosome
Baker, N., Sept, D., Joseph, S., Holst, M., & McCammon, J. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.181342398 · Cited by 7,125
MICROTUBULE POLYMERIZATION DYNAMICS
Desai, A. B., & Mitchison, T. J. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.83 · Cited by 2,660
Modulation of the dynamic instability of tubulin assembly by the microtubule-associated protein tau.
Drechsel, D. N., Hyman, A. A., Cobb, M. H., & Kirschner, M. W. (1992) · Molecular Biology of the Cell · doi:10.1091/mbc.3.10.1141 · Cited by 1,011
Control of microtubule organization and dynamics: Two ends in the limelight
Akhmanova, A., & Steinmetz, M. O. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4084 · Cited by 895
Cytoskeletal Dynamics and Transport in Growth Cone Motility and Axon Guidance
Dent, E. W., & Gertler, F. B. (2003) · Neuron · doi:10.1016/s0896-6273(03)00633-0 · Cited by 922
Metadata
- Authors
- Walker, R. A., O'Brien, E. T., Pryer, N. K., Soboeiro, M. F., Voter, W. A., Erickson, H. P., & Salmon, E. D.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Department of Biology, University of North Carolina, Chapel Hill 27599-3280.
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 1988-10-01
- Volume
- 107
- Issue
- 4
- Pages
- 1437-1448
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2115242
- OpenAlex
- W2015005644
- Cited by
- 980
- References
- 45
- Citations by year
- 2026: 10 · 2025: 14 · 2024: 19 · 2023: 22 · 2022: 37 · 2021: 27 · 2020: 27 · 2019: 43 · 2018: 35 · 2017: 30 · 2016: 36 · 2015: 34 · 2014: 31 · 2013: 23 · 2012: 23
- FWCI
- 10.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Cell Biology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (GM24364, GM 28553)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- microtubule dynamic instability, GTP cap, treadmilling
- MeSH terms
- Animals, Guanosine Triphosphate, Kinetics, Microtubules, Protein Binding, Swine, Tubulin, Video Recording, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review