Chapter title |
Analysis of mitotic protein dynamics and function in Drosophila embryos by live cell imaging and quantitative modeling.
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Chapter number | 1 |
Book title |
Mitosis
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Published in |
Methods in molecular biology, March 2014
|
DOI | 10.1007/978-1-4939-0329-0_1 |
Pubmed ID | |
Book ISBNs |
978-1-4939-0328-3, 978-1-4939-0329-0
|
Authors |
Brust-Mascher I, Civelekoglu-Scholey G, Scholey JM, Ingrid Brust-Mascher, Gul Civelekoglu-Scholey, Jonathan M. Scholey, Brust-Mascher, Ingrid, Civelekoglu-Scholey, Gul, Scholey, Jonathan M. |
Abstract |
Mitosis depends upon the mitotic spindle, a dynamic protein machine that uses ensembles of dynamic microtubules (MTs) and MT-based motor proteins to assemble itself, control its own length (pole-pole spacing), and segregate chromosomes during anaphase A (chromosome-to-pole motility) and anaphase B (spindle elongation). In this review, we describe how the molecular and biophysical mechanisms of these processes can be analyzed in the syncytial Drosophila embryo by combining (1) time-lapse imaging and other fluorescence light microscopy techniques to study the dynamics of mitotic proteins such as tubulins, mitotic motors, and chromosome or centrosome proteins; (2) the perturbation of specific mitotic protein function using microinjected inhibitors (e.g., antibodies) or mutants to infer protein function; and (3) mathematical modeling of the qualitative models derived from these experiments, which can then be used to make predictions which are in turn tested experimentally. We provide details of the methods we use for embryo preparation, fluorescence imaging, and mathematical modeling. |
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