Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-36977
Methods Mol Med 2007 Jan 01;137:29-43. doi: 10.1007/978-1-59745-442-1_3.
Show Gene links Show Anatomy links

Purification and mass spectrometry identification of microtubule-binding proteins from Xenopus egg extracts.

Gache V , Waridel P , Luche S , Shevchenko A , Popov AV .


???displayArticle.abstract???
Microtubule-binding proteins are conveniently divided into two large groups: MAPs (microtubule-associated proteins), which can stabilize, anchor, and/or nucleate microtubules, and motors, which use the energy of ATP hydrolysis for a variety of functions, including microtubule network organization and cargo transportation along microtubules. Here, we describe the use of Taxol-stabilized microtubules for purification of MAPs, motors, and their complexes from Xenopus egg extracts. Isolated proteins are analysed using sodium dodecyl sulfate gel electrophoresis and identified by various mass spectrometry and database mining technologies. Found proteins can be grouped into three classes: (1) known MAPs and motors; (2) proteins previously reported as associated with the microtubule cytoskeleton, but without a clearly defined cytoskeletal function; (3) proteins not yet described as having microtubule localization. Sequence-similarity methods employed for protein identification allow efficient identification of MAPs and motors from species with yet unsequenced genomes.

???displayArticle.pubmedLink??? 18085220
???displayArticle.pmcLink??? PMC2750007
???displayArticle.link??? Methods Mol Med
???displayArticle.grants??? [+]


References [+] :
Andersen, Balanced regulation of microtubule dynamics during the cell cycle: a contemporary view. 1999, Pubmed