De novo design of transmembrane accessory subunits for fold stabilization and expansion
Jojoa Cruz, S.; Kanwal, S.; Jacob, N. P.; Tang, W.; Murakoso, M.; Zhang, M.; Li, J.; Domecillo, M.; Polizzi, N.; Yates, J. R.; Kratochvil, H. T.; Gomes, F. P.; Hong, H.; Mravic, M.
Show abstract
Transmembrane (TM) proteins play essential roles in biology as transporters, ion channels, chaperones, enzymes, and mediators of signal transduction. However, membrane proteins often suffer from inefficient folding and intrinsic instability. Misfolding in cells can cause numerous loss-of-function pathologies. Likewise, denaturation upon purification in the laboratory is a critical barrier to structure determination and characterization of key biochemical mechanisms. Generalizable strategies to stabilize membrane proteins remain limited. Here, we developed an informatics-based de novo design strategy to create synthetic auxiliary subunits that interact with the TM helices of a model pentameric ion channel, thereby bolstering folding while maintaining channel function. Biochemical and structural characterization reveal the synthetic TM subunits can also be used to create larger multi-spanning designer proteins of custom topology. This proof-of-concept motivates the feasibility of computationally designed accessory TM helices as potential pharmacological chaperone "folding correctors" of membrane proteins in disease and as tools in structural biology.
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