Microtubules are widely distributed in eucaryotic cells and tissues, and are especially abundant in the central nervous system. They are essential to a large number of cellular processes, particularly those concerned with the development and maintenance of cell shape, changes in cell shape, and certain forms of cell motility. It is evident that microtubules must play vital roles in CNS function. For example, they appear to be essential to the development and maintenance of the asymmetric shape characteristic of neuronal cells; and it seems likely that they are involved in both slow and fast axoplasmic transport. However, there is as yet no biochemically defined knowledge as to what the true mechanistic functions of microtubules are, and the specific role(s) of microtubules in the CNS remain largely unknown. The main objectives of this research are to characterize brain microtubule (neurotubule) biochemistry and function with the use of two experimental approaches. One approach focuses on investigation of the biochemical properties of tubulin and other microtubule-associated proteins from the chick and bovine CNS. Some of the specific questions will be concerned with characterization of the subpopulations of microtubules in the CNS, and with regulation of opposite-end assembly and disassembly of brain microtubules. The second approach involves investigation of the biochemical mechanisms of action of drugs that inhibit microtubule polymerization. Studies on the interactions of drugs with tubulin not only yield information on the biochemical mechanisms of action of the drugs, but also provide valuable information on the biochemical properties and functional roles of microtubles. The purpose of these studies is to define the biochemical properties of microtubule protein which are related to microtubule functions, with the long-term goal of understanding the roles of microtubules in relation to brain function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS013560-10
Application #
3395257
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1978-07-01
Project End
1986-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
10
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of California Santa Barbara
Department
Type
Schools of Arts and Sciences
DUNS #
City
Santa Barbara
State
CA
Country
United States
Zip Code
93106
Choi, Myung Chul; Chung, Peter J; Song, Chaeyeon et al. (2017) Paclitaxel suppresses Tau-mediated microtubule bundling in a concentration-dependent manner. Biochim Biophys Acta Gen Subj 1861:3456-3463
Chung, Peter J; Song, Chaeyeon; Deek, Joanna et al. (2016) Tau mediates microtubule bundle architectures mimicking fascicles of microtubules found in the axon initial segment. Nat Commun 7:12278
Chung, Peter J; Choi, Myung Chul; Miller, Herbert P et al. (2015) Direct force measurements reveal that protein Tau confers short-range attractions and isoform-dependent steric stabilization to microtubules. Proc Natl Acad Sci U S A 112:E6416-25
Ojeda-Lopez, Miguel A; Needleman, Daniel J; Song, Chaeyeon et al. (2014) Transformation of taxol-stabilized microtubules into inverted tubulin tubules triggered by a tubulin conformation switch. Nat Mater 13:195-203
Needleman, Daniel J; Ojeda-Lopez, Miguel A; Raviv, Uri et al. (2013) Ion specific effects in bundling and depolymerization of taxol-stabilized microtubules. Faraday Discuss 166:31-45
Lopus, Manu; Manatschal, Cristina; Buey, Ruben M et al. (2012) Cooperative stabilization of microtubule dynamics by EB1 and CLIP-170 involves displacement of stably bound P(i) at microtubule ends. Biochemistry 51:3021-30
Lopus, Manu (2011) Antibody-DM1 conjugates as cancer therapeutics. Cancer Lett 307:113-8
Davé, Rahul H; Saengsawang, Witchuda; Lopus, Manu et al. (2011) A molecular and structural mechanism for G protein-mediated microtubule destabilization. J Biol Chem 286:4319-28
Safinya, Cyrus R; Raviv, Uri; Needleman, Daniel J et al. (2011) Nanoscale assembly in biological systems: from neuronal cytoskeletal proteins to curvature stabilizing lipids. Adv Mater 23:2260-70
Kiris, Erkan; Ventimiglia, Donovan; Sargin, Mehmet E et al. (2011) Combinatorial Tau pseudophosphorylation: markedly different regulatory effects on microtubule assembly and dynamic instability than the sum of the individual parts. J Biol Chem 286:14257-70

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