posted on 2022-05-23, 16:09authored byWadim Weber, Markus Roeder, Tobias Probanowski, Jie Yang, Helal Abujubara, Heinz Koeppl, Alesia Tietze, Viktor Stein
Nanopores comprise a versatile class
of membrane proteins that
carry out a range of key physiological functions and are increasingly
developed for different biotechnological applications. Yet, a capacity
to study and engineer protein nanopores by combinatorial means has
so far been hampered by a lack of suitable assays that combine sufficient
experimental resolution with throughput. Addressing this technological
gap, the functional nanopore (FuN) screen now provides a quantitative
and dynamic readout of nanopore assembly and function in the context
of the inner membrane of Escherichia coli. The assay is based on genetically encoded fluorescent protein sensors
that resolve the nanopore-dependent influx of Ca2+ across
the inner membrane of E. coli. Illustrating
its versatile capacity, the FuN screen is first applied to dissect
the molecular features that underlie the assembly and stability of
nanopores formed by the S2168 holin. In a subsequent step,
nanopores are engineered by recombining the transmembrane module of
S2168 with different ring-shaped oligomeric protein structures
that feature defined hexa-, hepta-, and octameric geometries. Library
screening highlights substantial plasticity in the ability of the
S2168 transmembrane module to oligomerize in alternative
geometries, while the functional properties of the resultant nanopores
can be fine-tuned through the identity of the connecting linkers.
Overall, the FuN screen is anticipated to facilitate both fundamental
studies and complex nanopore engineering endeavors with many potential
applications in biomedicine, biotechnology, and synthetic biology.