Assay of Rab4-dependent trafficking on microtubules.

Abstract:

:We present an in vitro method to measure how Rab4 and other regulatory proteins affect microtubule-based organelle motility. The protocols utilize small-volume, disposable "microchambers" designed for epifluorescence, confocal, or other microscope platforms and into which microtubules, organelles, and primary and fluorescent secondary antibodies are added. Our work has focused on the isolation and use of endocytic vesicles from rat liver, and we present these protocols. However, the techniques can be adapted for other organelles or cell types. Multiple fluorescent probes, rapid image capture, and immunofluorescence under non-fixation conditions allow for measurements of the location and intensity changes of endogenous proteins upon addition of ATP or upon addition of other proteins or regulatory factors. We review measurements of microtubule-based motility as well as measurements for protein localization and protein segregation in vitro.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Murray JW,Wolkoff AW

doi

10.1016/S0076-6879(05)03009-0

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

92-107

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(05)03009-0

journal_volume

403

pub_type

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