BECAUSE of its high degree of specificity1, the binding of colchicine to tubulin has become a powerful tool for the quantification and subcellular localisation of the protein. The mechanism of the binding reaction is not yet completely understood, but several of its characteristics are well documented. One of these is the decay of binding capacity with time, which follows the kinetics of a firstorder reaction2,3 and is accentuated at elevated temperatures4. Although correlation between this rate of decay and the loss of other characteristic functions of tubulin, such as its ability to polymerise into microtubules, has not been directly established by experiment, carefully con trolled measurements of the decay of colchicine binding seem to be useful for estimating the stability of the tubulin molecules per se. In contrast, the decay rate of the polymerisability of tubulin preparations should depend not only on the stability of the tubulin molecules themselves but also on that of other factors that may be essential for polymerisation5–7. As part of our recently initiated8,9 attempt to study the mechanisms regulating microtubule assembly in cultured cells, we report here that tubulin preparations from rat glial C6 cells exhibit a decay rate of colchicine-binding activity that is quite different from the decay rate of polymerisability.
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WICHE, G., HONIG, L. & COLE, R. Polymerising ability of C6 glial cell microtubule protein decays much faster than its colchicine-binding activity. Nature 269, 435–436 (1977). https://doi.org/10.1038/269435a0
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