Microtubules capture chromosomes during mitosis by stochastically switching between growth and shrinkage at catastrophe events. They display strikingly rich biochemistry and dynamics, regulated by a stabilizing cap with distinct conformational states. Microtubule lengths at catastrophe are observed to follow a peaked distribution, while their growth “stutters” briefly before catastrophe. Such complexity makes it hard to capture all these observations without a large number of tunable parameters. Here, we introduce a topological model of the microtubule cap that reproduces the features above through dynamical edge states, that provides a minimal description with just two free parameters. Our approach further provides an analytical description of catastrophes and allows the same features to persist over a wide range of tubulin concentration, consistent with experimental observations.

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