Tau-isoform dependent enhancement of taxol mobility through microtubules

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Tau, a family of microtubule-associated proteins (MAPS), stabilizes microtubules (MTs) and regulates their dynamics. Tau isoforms regulate MT dynamic instability differently: 3-repeat tau is less effective than 4-repeat tau at Suppressing the disassembly of MTs. Here, we report another tau-isoforn-dependent phenomenon, revealed by fluorescence recovery after photobleaching measurements on a BODIPY-conjugated taxol bound to MTs. Saturating levels of recombinant full-length 3-repeat and 4-repeat tau both cause taxol mobility to be remarkably sensitive to taxol concentration. However, 3-repeat tau induces 2.5-fold faster recovery (similar to 450 s) at low taxol concentrations (similar to 100 nM) than 4-repeat tau (similar to 1000 s), indicating that 3-repeat tau decreases the probability of taxol rebinding to its site in the MT lumen. Finding no tau-induced change in the MT-binding affinity Of taxol, We Conclude that 3-repeat tau either competes for the taxol binding site with an affinity of similar to 1 mu M or alters the MT structure so as to facilitate the passage of taxol through Pores in the MT wall. (c) 2008 Elsevier Inc. All rights reserved.
Publisher
ELSEVIER SCIENCE INC
Issue Date
2008-10
Language
English
Article Type
Article
Keywords

PAIRED HELICAL FILAMENTS; PROTEIN-TAU; NEURODEGENERATIVE DISEASE; BINDING; SURFACE; PROTOFILAMENTS; 3-REPEAT-TAU; 4-REPEAT-TAU; DYNAMICS; DOMAINS

Citation

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, v.478, no.1, pp.119 - 126

ISSN
0003-9861
DOI
10.1016/j.abb.2008.07.020
URI
http://hdl.handle.net/10203/19353
Appears in Collection
PH-Journal Papers(저널논문)
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