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Title

Zampanolide binding to tubulin indicates crosstalk of taxane site with colchicine and nucleotide sites

AuthorsField, Jessica J.; Pera, Benet ; Estévez-Gallego, Juan ; Rodríguez-Salarichs, Javier; Sáez-Calvo, Gonzalo; Andreu, José Manuel ; Díaz, José Fernando
Issue Date12-Oct-2017
PublisherAmerican Chemical Society
CitationJ. Nat. Prod., Article ASAP (2017)
AbstractThe marine natural product zampanolide and analogues thereof constitute a new chemotype of taxoid site microtubule-stabilizing agents with a covalent mechanism of action. Zampanolide-ligated tubulin has the switch-activation loop (M-loop) in the assembly prone form and, thus, represents an assembly activated state of the protein. In this study, we have characterized the biochemical properties of the covalently modified, activated tubulin dimer, and we have determined the effect of zampanolide on tubulin association and the binding of tubulin ligands at other binding sites. Tubulin activation by zampanolide does not affect its longitudinal oligomerization but does alter its lateral association properties. The covalent binding of zampanolide to β-tubulin affects both the colchicine site, causing a change of the quantum yield of the bound ligand, and the exchangeable nucleotide binding site, reducing the affinity for the nucleotide. While these global effects do not change the binding affinity of 2-methoxy-5-(2,3,4-trimethoxyphenyl)-2,4,6-cycloheptatrien-1-one (MTC) (a reversible binder of the colchicine site), the binding affinity of a fluorescent analogue of GTP (Mant-GTP) at the nucleotide E-site is reduced from 12 ± 2 × 105 M-1 in the case of unmodified tubulin to 1.4 ± 0.3 × 105 M-1 in the case of the zampanolide tubulin adduct, indicating signal transmission between the taxane site and the colchicine and nucleotide sites of β-tubulin.
Description41 p.-8 fig.-2 tab. Field, Jessica J. et al.
Publisher version (URL)http://dx.doi.org/10.1021/acs.jnatprod.7b00704
URIhttp://hdl.handle.net/10261/156392
DOI10.1021/acs.jnatprod.7b00704
ISSN0163-3864
E-ISSN1520-6025
Appears in Collections:(CIB) Artículos
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