Multicomponent rendezvous of cofilin, profilin and twinfilin at the actin filament barbed end

TL;DR

This study investigates how profilin, cofilin, and twinfilin collectively regulate actin filament depolymerization at the barbed end, revealing new interactions and mechanisms through combined experimental and theoretical approaches.

Contribution

It provides novel insights into the multicomponent regulation of actin filament dynamics by simultaneously visualizing and modeling the interactions of three key proteins.

Findings

Twinfilin competes with profilin and promotes cofilin binding.

Profilin and cofilin can bind simultaneously to the filament barbed end.

Their combined action accelerates filament depolymerization.

Abstract

Cellular actin dynamics result from collective action of hundreds of regulatory proteins, majority of which target actin filaments at their barbed ends. Three key actin binding proteins - profilin, cofilin and twinfilin individually depolymerize filament barbed ends. Notwithstanding recent leaps in our understanding of their individual action, how they collectively regulate filament dynamics remains an open question. In absence of direct and simultaneous visualization of these proteins at barbed ends, gaining mechanistic insights has been challenging. We have here investigated multicomponent dynamics of profilin, cofilin and twinfilin using a hybrid approach that combines high throughput single filament experiments with theory. We discovered that while twinfilin competes with profilin, it promotes binding of cofilin to filament sides. Interestingly, contrary to previous expectations, we found that profilin and cofilin can simultaneously bind the same filament barbed end resulting in its accelerated depolymerization. Our study reveals that pair-wise interactions can effectively capture depolymerization dynamics in simultaneous presence of all three proteins. We thus believe that our approach of employing a theory-experiment dialog can potentially help decipher multicomponent regulation of actin dynamics.