Skip to main content
. 2017 Jul 3;114(29):E5950–E5958. doi: 10.1073/pnas.1705062114

Fig. S2.

Fig. S2.

Pelleting assay showing stoichiometric binding of PdBtubC to PdBtubAB filaments. Replicate experiment to the one shown in Fig. 1D. Fourfold excess of BtubC to BtubAB (molar, C to AB heterodimer) leads to roughly the same amount of BtubC in the pellet compared with equimolar quantities. Excess BtubC protein remains in the supernatant and does not spin down, indicating a specific interaction of BtubC with BtubAB heterodimers in the filaments.