Goldmacher, Victor S.Audette, Charlene A.Guan, YinghuaSidhom, Eriene-HeidiShah, JageshWhiteman, Kathleen R.Kovtun, Yelena V.2015-03-022015Goldmacher, Victor S., Charlene A. Audette, Yinghua Guan, Eriene-Heidi Sidhom, Jagesh V. Shah, Kathleen R. Whiteman, and Yelena V. Kovtun. 2015. “High-Affinity Accumulation of a Maytansinoid in Cells via Weak Tubulin Interaction.” PLoS ONE 10 (2): e0117523. doi:10.1371/journal.pone.0117523. http://dx.doi.org/10.1371/journal.pone.0117523.1932-6203http://nrs.harvard.edu/urn-3:HUL.InstRepos:14065542The microtubule-targeting maytansinoids accumulate in cells and induce mitotic arrest at 250- to 1000-fold lower concentrations than those required for their association with tubulin or microtubules. To identify the mechanisms of this intracellular accumulation and exceptional cytotoxicity of maytansinoids we studied interaction of a highly cytotoxic maytansinoid, S-methyl DM1 and several other maytansinoids with cells. S-methyl DM1 accumulated inside the cells with a markedly higher apparent affinity than to tubulin or microtubules. The apparent affinities of maytansinoids correlated with their cytotoxicities. The number of intracellular binding sites for S-methyl DM1 in MCF7 cells was comparable to the number of tubulin molecules per cell (~ 4–6 × 107 copies). Efflux of 3 [H]-S-methyl DM1 from cells was enhanced in the presence of an excess of non-labeled S-methyl DM1, indicating that re-binding of 3 [H]-S-methyl DM1 to intracellular binding sites contributed to its intracellular retention. Liposomes loaded with non-polymerized tubulin recapitulated the apparent high-affinity association of S-methyl DM1 to cells. We propose a model for the intracellular accumulation of maytansinoids in which molecules of the compounds diffuse into a cell and associate with tubulin. Affinities of maytansinoids for individual tubulin molecules are weak, but the high intracellular concentration of tubulin favors, after dissociation of a compound-tubulin complex, their re-binding to a tubulin molecule, or to a tip of a microtubule in the same cell, over their efflux. As a result, a significant fraction of microtubule tips is occupied with a maytansinoid when added to cells at sub-nanomolar concentrations, inducing mitotic arrest and cell death.en-USJournal Article2015-03-0210.1371/journal.pone.0117523