A taxol-dependent procedure for the isolation of microtubules and microtubule-associated proteins (MAPs).
Open accessAbstract
The effect of the antimitotic drug taxol on the association of MAPs (microtubule-associated proteins) with microtubules was investigated. Extensive microtubule assembly occurred in the presence of Taxol at 37 degrees C. at 0 degrees C, and at 37 degrees C in the presence of 0.35 M NaCl, overcoming the inhibition of assembly normally observed under the latter two conditions. At 37 degrees C and at 0 degrees C, complete assembly of both tubulin and the MAPs was observed in the presence of Taxol. However, at elevated ionic strength, only tubulin assembled, forming microtubules devoid of MAPs. The MAPs could also be released from the surface of preformed microtubules by exposure to elevated ionic strength. These properties provided the basis for a rapid new procedure for isolating microtubules and MAPs of high purity from small amounts of biological material. The MAPs could be recovered by exposure of the microtubules to elevated ionic strength and subjected to further analysis. Microtubules and MAPs were prepared from bovine cerebral cortex (gray matter) and from HeLa cells. MAP 1, MAP2, and the tau MAPs, as well as species of Mr = 28,000 and 30,000 (LMW, or low molecular weight, MAPs) and a species of Mr = 70,000 were isolated from gray matter. Species identified as the 210,000 and 125,000 mol wt HeLa MAPs were isolated from HeLa cells. Microtubules were also prepared for the first time from white matter. All of the MAPs identified in gray matter preparations were identified in white matter, but the amounts of individual MAP species differed. The most striking difference in the two preparations was a fivefold lower level of MAP 2 relative to tubulin in white matter than in gray. The high molecular weigh MAP, MAP1, was present in equal ratio to tubulin in white and gray matter. These results indicate that MAP 1 and MAP2, as well as other MAP species, may have a different cellular or subcellular distribution.
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MAP2 is preferentially distributed in gray matter.
“This is consistent with its preferential distribution in gray matter, as has been shown biochemically (Vallee, 1982).”
From Immunocytochemical localization of tubulin and microtubule-associated protein 2 during the development of hippocampal neurons in culture (1986) · cites this paper as Vallee, 1982
There are molecular differences between microtubules and neurofilaments in different regions of a neuron and in different classes of neurons.
“In addition, recent biochemical and immunocytochemical studies have established that there are molecular differences between the microtubules (Caceres et al., 1984b;Matus et al., 198 1;Vallee, 1982) and neurofilaments (Hirokawa et al., 1984;Shaw et al., 198 1) in different regions of a neuron, and in different classes of neurons (Goldstein et al., 1983).”
From Immunocytochemical localization of tubulin and microtubule-associated protein 2 during the development of hippocampal neurons in culture (1986) · cites this paper as Vallee, 1982
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Tubulin requires tau for growth onto microtubule initiating sites.
Witman, G. B., Cleveland, D. W., Weingarten, M. D., & Kirschner, M. W. (1976) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.73.11.4070 · Cited by 238 · see citing works
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Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility
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Phosphorylation affects the ability of tau protein to promote microtubule assembly.
Lindwall, G., & Cole, R. D. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)42989-9 · Cited by 901 · see citing works
The microtubule binding domain of tau protein
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Self-citationCaceres, A., Banker, G., & Binder, L. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-03-00714.1986 · Cited by 367 · see citing works
Single-molecule investigation of the interference between kinesin, tau and MAP2c
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Microtubule-associated protein-dependent binding of phagosomes to microtubules
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- Authors
- Vallee, R. B.
- Corresponding author
- Vallee, R B
- ORCID
- Vallee, R B
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1982-02-01
- Volume
- 92
- Issue
- 2
- Pages
- 435-442
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2112074
- OpenAlex
- W2032342779
- Cited by
- 551
- References
- 1
- Citations by year
- 2023: 3 · 2022: 1 · 2021: 1 · 2020: 4 · 2019: 2 · 2017: 3 · 2016: 3 · 2015: 1 · 2014: 2 · 2013: 1 · 2012: 2
- FWCI
- 17.11
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Cell Biology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
- Physical Sciences › Chemistry › Organic Chemistry › Synthesis and biological activity
- Keywords
- microtubules, microtubule-associated proteins, paclitaxel, microtubule assembly, ionic strength, MAP1, MAP2, tau protein, bovine cerebral cortex, HeLa cells, white matter, gray matter, subcellular localization, protein extraction
- MeSH terms
- Alkaloids, Animals, Brain, Cattle, Cell-Free System, Microtubule-Associated Proteins, Microtubules, Protein Binding, Proteins, Temperature, Paclitaxel
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