| Literature DB >> 31879896 |
Annapurna Vemu1, Ewa Szczesna1, Antonina Roll-Mecak2,3.
Abstract
Microtubules are non-covalent dynamic polymers essential for the life of all eukaryotic cells. Their dynamic behavior is regulated by a large array of cellular effectors. In vitro microtubule assays have been instrumental in dissecting the mechanism of microtubule-associated proteins. In this chapter, we focus on microtubule-severing enzymes katanin and spastin. They are AAA ATPases that generate internal breaks in microtubules by extracting tubulin dimers out of the microtubule lattice. We present protocols for TIRF microscopy-based assays that were instrumental in proving that these enzymes not only sever microtubules but also remodel the microtubule lattice by promoting the exchange of lattice GDP-tubulin with GTP-tubulin from the soluble pool. This activity can modulate microtubule dynamics and support microtubule-dependent microtubule amplification in the absence of a nucleating factor.Entities:
Keywords: AAA ATPase; Cytoskeleton; GTP-tubulin; Katanin; Microtubule; Microtubule dynamics; Microtubule repair; Microtubule severing; Rescue; Spastin
Year: 2020 PMID: 31879896 PMCID: PMC7153568 DOI: 10.1007/978-1-0716-0219-5_3
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745