7NFO
A hexameric barrel state of a de novo coiled-coil assembly: CC-Type2-(LaId)4-I17C.
Summary for 7NFO
Entry DOI | 10.2210/pdb7nfo/pdb |
Descriptor | CC-Type2-(LaId)4-I17C (2 entities in total) |
Functional Keywords | coiled coil, synthetic peptide, homomeric assembly, de novo protein |
Biological source | synthetic construct |
Total number of polymer chains | 3 |
Total formula weight | 9674.57 |
Authors | Rhys, G.G.,Dawson, W.M.,Brady, R.L.,Woolfson, D.N. (deposition date: 2021-02-07, release date: 2022-03-02, Last modification date: 2024-05-01) |
Primary citation | Dawson, W.M.,Shelley, K.L.,Fletcher, J.M.,Scott, D.A.,Lombardi, L.,Rhys, G.G.,LaGambina, T.J.,Obst, U.,Burton, A.J.,Cross, J.A.,Davies, G.,Martin, F.J.O.,Wiseman, F.J.,Brady, R.L.,Tew, D.,Wood, C.W.,Woolfson, D.N. Differential sensing with arrays of de novo designed peptide assemblies. Nat Commun, 14:383-383, 2023 Cited by PubMed Abstract: Differential sensing attempts to mimic the mammalian senses of smell and taste to identify analytes and complex mixtures. In place of hundreds of complex, membrane-bound G-protein coupled receptors, differential sensors employ arrays of small molecules. Here we show that arrays of computationally designed de novo peptides provide alternative synthetic receptors for differential sensing. We use self-assembling α-helical barrels (αHBs) with central channels that can be altered predictably to vary their sizes, shapes and chemistries. The channels accommodate environment-sensitive dyes that fluoresce upon binding. Challenging arrays of dye-loaded barrels with analytes causes differential fluorophore displacement. The resulting fluorimetric fingerprints are used to train machine-learning models that relate the patterns to the analytes. We show that this system discriminates between a range of biomolecules, drink, and diagnostically relevant biological samples. As αHBs are robust and chemically diverse, the system has potential to sense many analytes in various settings. PubMed: 36693847DOI: 10.1038/s41467-023-36024-y PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.37 Å) |
Structure validation
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