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Ultrastructural analysis of the dynactin complex: an actin-related protein is a component of a filament that resembles F-actin.
Open accessAbstract
The dynactin complex visualized by deepetch electron microscopy appears as a short filament 37-nm in length, which resembles F-actin, plus a thinner, laterally oriented filament that terminates in two globular heads. The locations of several of the constituent polypeptides were identified on this structure by applying antibodies to decorate the dynactin complex before processing for electron microscopy. Antibodies to the actin-related protein Arp1 (previously referred to as actin-RPV), bound at various sites along the filament, demonstrating that this protein assembles in a polymer similar to conventional actin. Antibodies to the barbed-end actin-binding protein, capping protein, bound to one end of the filament. Thus, an actin-binding protein that binds conventional actin may also bind to Arp1 to regulate its polymerization. Antibodies to the 62-kD component of the dynactin complex also bound to one end of the filament. An antibody that binds the COOH-terminal region of the 160/150-kD dynactin polypeptides bound to the globular domains at the end of the thin lateral filament, suggesting that the dynactin polypeptide comprises at least part of the sidearm structure.
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Cited by
Echeverri, C. J., Paschal, B. M., Vaughan, K. T., & Vallee, R. B. (1996) · The Journal of cell biology · doi:10.1083/jcb.132.4.617 · Cited by 632
Axonal transport and neurodegenerative disease
Chevalier-Larsen, E., & Holzbaur, E. L. F. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2006.04.002 · Cited by 438
The structure of the dynactin complex and its interaction with dynein
Urnavicius, L., Zhang, K., Diamant, A. G., Motz, C., Schlager, M. A., Yu, M., Patel, N. A., Robinson, C. V., & Carter, A. P. (2015) · Science · doi:10.1126/science.aaa4080 · Cited by 421
Opposing motor activities are required for the organization of the mammalian mitotic spindle pole.
Gaglio, T., Saredi, A., Bingham, J. B., Hasbani, M. J., Gill, S. R., Schroer, T. A., & Compton, D. A. (1996) · The Journal of cell biology · doi:10.1083/jcb.135.2.399 · Cited by 290
Self-citationMack, G. J., & Compton, D. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.261371298 · Cited by 157
Metadata
- Authors
- Schafer, D. A., Gill, S. R., Cooper, J. A., Heuser, J. E., & Schroer, T. A.
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1994-07-15
- Volume
- 126
- Issue
- 2
- Pages
- 403-412
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2079164473
- Cited by
- 280
- References
- 0
- FWCI
- 7.63
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Ultrastructural analysis of the dynactin complex: an actin-related protein is a component of a filament that resembles F-actin. https://app.cochat.ai/papers/10.1083/jcb.126.2.403
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- Schafer, D. A., Gill, S. R., Cooper, J. A., Heuser, J. E., & Schroer, T. A. (1994). Ultrastructural analysis of the dynactin complex: an actin-related protein is a component of a filament that resembles F-actin. The Journal of cell biology. https://doi.org/10.1083/jcb.126.2.403
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.