Using STADIA to quantify dynamic instability in microtubules.

Automated analysis Dynamic instability Microtubules Stutter k-Means clustering

Journal

Methods in cell biology
ISSN: 0091-679X
Titre abrégé: Methods Cell Biol
Pays: United States
ID NLM: 0373334

Informations de publication

Date de publication:
2020
Historique:
entrez: 20 5 2020
pubmed: 20 5 2020
medline: 9 7 2021
Statut: ppublish

Résumé

Quantification of microtubule (MT) dynamic instability (DI) is essential to mechanistic dissection of MT assembly and the activities of MT binding proteins. Typical methods for quantifying MT dynamics assume that MT behavior consists of growth and shortening phases, with instantaneous transitions (rescues and catastrophes) in between. However, examination of DI data at high temporal and spatial resolution reveals the presence of ambiguous behaviors that cannot easily fit into these categories. Failure to objectively recognize and quantify these behaviors could reduce the reproducibility of DI data and impact attempts to dissect mechanisms. To address these problems, we recently developed STADIA (Statistical Tool for Automated Dynamic Instability Analysis), a MT analysis software package that uses length-history data as input and is (presently) implemented in MATLAB. STADIA uses machine learning methods to objectively analyze and quantify macro-level DI behaviors exhibited by MTs, including variable rates of growth and shortening and a newly quantified DI phase: stutter. Here we overview the process of using STADIA to quantify MT dynamics and provide a set of concrete protocols for using STADIA to process and analyze MT length history data.

Identifiants

pubmed: 32423646
pii: S0091-679X(20)30015-7
doi: 10.1016/bs.mcb.2020.03.002
pii:
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

117-143

Subventions

Organisme : National Science Foundation
ID : MCB 1817966
Pays : International
Organisme : National Science Foundation
ID : PHY 1806631
Pays : International
Organisme : National Science Foundation
ID : DGE-1313583
Pays : International

Informations de copyright

© 2020 Elsevier Inc. All rights reserved.

Auteurs

Riya J Patel (RJ)

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, United States; Penn High School, Mishawaka, IN, United States; Indiana University, Bloomington, IN, United States.

Kristopher S Murray (KS)

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, United States.

Peter O Martin (PO)

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, United States; Trinity School at Greenlawn, South Bend, IN, United States.

Michael Sinclair (M)

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, United States; Kalamazoo Area Mathematics & Science Center, Kalamazoo, MI, United States.

Jared P Scripture (JP)

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, United States.

Holly V Goodson (HV)

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, United States. Electronic address: hgoodson@nd.edu.

Shant M Mahserejian (SM)

Pacific Northwest National Laboratory, Richland, WA, United States.

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Classifications MeSH