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. 2021 Jan 27;12:609. doi: 10.1038/s41467-020-20873-y

Fig. 1. Model description.

Fig. 1

a Schematic representation of an sPG synthase complex’s interaction with FtsZ treadmilling. FtsZ resides in the cytoplasm. FtsI is a transmembrane protein that does not dissociate from the membrane even when it dissociates from FstZ. b Model simplification of FtsZ–FtsI interaction at the septum. The FtsZ filament (purple) undergoes treadmilling by dissociating an FtsZ subunit from the left end and associating new ones on the right end. While FtsI (gray) intrinsically diffuses around, it has a binding affinity to FtsZ subunits. c Schematics of FtsZ–FtsI binding potentials. Here, the binding potential is assumed to be harmonic and short-ranged (~5 nm), which is about the size of an individual FtsZ subunit. Note that there is no energy barrier for FtsI to bind to FtsZ, because the binding potential is attractive. Once FtsI binds to an FtsZ subunit, however, the binding potential presents an energetic barrier preventing FtsI from diffusing away.