Your browser doesn't support javascript.
loading
Manipulation and quantification of microtubule lattice integrity.
Reid, Taylor A; Coombes, Courtney; Gardner, Melissa K.
Afiliación
  • Reid TA; Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455, USA.
  • Coombes C; Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455, USA.
  • Gardner MK; Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455, USA klei0091@umn.edu.
Biol Open ; 6(8): 1245-1256, 2017 Aug 15.
Article en En | MEDLINE | ID: mdl-28663236
ABSTRACT
Microtubules are structural polymers that participate in a wide range of cellular functions. The addition and loss of tubulin subunits allows the microtubule to grow and shorten, as well as to develop and repair defects and gaps in its cylindrical lattice. These lattice defects act to modulate the interactions of microtubules with molecular motors and other microtubule-associated proteins. Therefore, tools to control and measure microtubule lattice structure will be invaluable for developing a quantitative understanding of how the structural state of the microtubule lattice may regulate its interactions with other proteins. In this work, we manipulated the lattice integrity of in vitro microtubules to create pools of microtubules with common nucleotide states, but with variations in structural states. We then developed a series of novel semi-automated analysis tools for both fluorescence and electron microscopy experiments to quantify the type and severity of alterations in microtubule lattice integrity. These techniques will enable new investigations that explore the role of microtubule lattice structure in interactions with microtubule-associated proteins.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Biol Open Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Biol Open Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos