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6YAZ

Crystal structure of a parallel hexameric coiled coil CC-Type2-(TaId)5

Summary for 6YAZ
Entry DOI10.2210/pdb6yaz/pdb
DescriptorCC-Type2-(TaId)5 (2 entities in total)
Functional Keywordsalpha-helical barrel, de novo protein, de novo peptide, coiled coil, designed peptide, designed protein
Biological sourcesynthetic construct
Total number of polymer chains12
Total formula weight47153.93
Authors
Scott, A.J.,Brady, R.L.,Woolfson, D.N. (deposition date: 2020-03-15, release date: 2021-04-07, Last modification date: 2024-11-13)
Primary citationScott, A.J.,Niitsu, A.,Kratochvil, H.T.,Lang, E.J.M.,Sengel, J.T.,Dawson, W.M.,Mahendran, K.R.,Mravic, M.,Thomson, A.R.,Brady, R.L.,Liu, L.,Mulholland, A.J.,Bayley, H.,DeGrado, W.F.,Wallace, M.I.,Woolfson, D.N.
Constructing ion channels from water-soluble alpha-helical barrels.
Nat.Chem., 13:643-650, 2021
Cited by
PubMed Abstract: The design of peptides that assemble in membranes to form functional ion channels is challenging. Specifically, hydrophobic interactions must be designed between the peptides and at the peptide-lipid interfaces simultaneously. Here, we take a multi-step approach towards this problem. First, we use rational de novo design to generate water-soluble α-helical barrels with polar interiors, and confirm their structures using high-resolution X-ray crystallography. These α-helical barrels have water-filled lumens like those of transmembrane channels. Next, we modify the sequences to facilitate their insertion into lipid bilayers. Single-channel electrical recordings and fluorescent imaging of the peptides in membranes show monodisperse, cation-selective channels of unitary conductance. Surprisingly, however, an X-ray structure solved from the lipidic cubic phase for one peptide reveals an alternative state with tightly packed helices and a constricted channel. To reconcile these observations, we perform computational analyses to compare the properties of possible different states of the peptide.
PubMed: 33972753
DOI: 10.1038/s41557-021-00688-0
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.94 Å)
Structure validation

237735

数据于2025-06-18公开中

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