Enhanced hexamerization of insulin via assembly pathway rerouting revealed by single particle studies

Bohr, F.; Bohr, S. S. R.; Mishra, N. K.; Foutel, N. S. G.; Pinholt, H. D.; Wu, S.; Nirlsen, E. M.; Zhang, M.; Kjaergaard, M.; Jensen, K. J.; Hatzakis, N. S.

doi:10.1101/2022.04.06.487286

bioRxiv · 10.1101/2022.04.06.487286

Enhanced hexamerization of insulin via assembly pathway rerouting revealed by single particle studies

Bohr, F.·Bohr, S. S. R.·Mishra, N. K.·Foutel, N. S. G.·Pinholt, H. D.·Wu, S.·Nirlsen, E. M.·Zhang, M.·Kjaergaard, M.·Jensen, K. J.·Hatzakis, N. S.

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Abstract

Insulin formulations are the hallmark of interventions for treatment of diabetes. Understanding the mechanism that governs insulin self assembly or disassembly --and the role of stabilizing additives--are essential for improving insulin formulations. We report here the real-time direct observation of single insulin self-assembly and disassembly events using single molecule fluorescence microscopy. Our direct observations revealed previously unaccounted monomeric additions to occur to all types of assemblies and allowed us to quantify the existence, abundance and kinetic characterization of diverse assembly pathways involving monomeric dimers or tetrameric insulin species. We proposed and experimentally validated a model where the insulin self-assembly pathway is rerouted favoring monomeric or oligomeric assembly events by solution concentration, additives and formulations. Our rate simulation predicted the abundance of each oligomeric species across a concentration range of 6 orders of magnitude. Besides providing fundamental new insights, the results and toolbox here can be universally applied contributing to the development of optimal insulin formulations and the deciphering of oligomerization mechanisms for other proteins.

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Bohr, F., Bohr, S. S. R., Mishra, N. K., Foutel, N. S. G., Pinholt, H. D., Wu, S., Nirlsen, E. M., Zhang, M., Kjaergaard, M., Jensen, K. J., Hatzakis, N. S.. 2022-04-08. Enhanced hexamerization of insulin via assembly pathway rerouting revealed by single particle studies. https://doi.org/10.1101/2022.04.06.487286

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