Abstract:
:CLASPs are mammalian microtubule-stabilizing proteins that can mediate the interaction between distal microtubule ends and the cell cortex. Using mass spectrometry-based assays, we have identified two CLASP partners, LL5beta and ELKS. LL5beta and ELKS form a complex that colocalizes with CLASPs at the cortex of HeLa cells as well as at the leading edge of motile fibroblasts. LL5beta is required for cortical CLASP accumulation and microtubule stabilization in HeLa cells, while ELKS plays an accessory role in these processes. LL5beta is a phosphatidylinositol-3,4,5-triphosphate (PIP3) binding protein, and its recruitment to the cell cortex is influenced by PI3 kinase activity but does not require intact microtubules. Cortical clusters of LL5beta and ELKS do not overlap with focal adhesions but often form in their vicinity and can affect their size. We propose that LL5beta and ELKS can form a PIP3-regulated cortical platform to which CLASPs attach distal microtubule ends.
journal_name
Dev Celljournal_title
Developmental cellauthors
Lansbergen G,Grigoriev I,Mimori-Kiyosue Y,Ohtsuka T,Higa S,Kitajima I,Demmers J,Galjart N,Houtsmuller AB,Grosveld F,Akhmanova Adoi
10.1016/j.devcel.2006.05.012subject
Has Abstractpub_date
2006-07-01 00:00:00pages
21-32issue
1eissn
1534-5807issn
1878-1551pii
S1534-5807(06)00252-8journal_volume
11pub_type
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