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8BCS

X-ray crystal structure of a de novo designed helix-loop-helix homodimer in an anti arrangement, CC-HP1.0

Summary for 8BCS
Entry DOI10.2210/pdb8bcs/pdb
DescriptorCC-HP1.0, ACETATE ION (2 entities in total)
Functional Keywordscoiled coil, 4-helix bundle, de novo protein design, helix-loop-helix dimer, de novo protein
Biological sourcesynthetic construct
Total number of polymer chains1
Total formula weight5334.31
Authors
Edgell, C.L.,Mylemans, B.,Naudin, E.A.,Smith, A.J.,Savery, N.J.,Woolfson, D.N. (deposition date: 2022-10-17, release date: 2023-06-07, Last modification date: 2024-10-16)
Primary citationSmith, A.J.,Naudin, E.A.,Edgell, C.L.,Baker, E.G.,Mylemans, B.,FitzPatrick, L.,Herman, A.,Rice, H.M.,Andrews, D.M.,Tigue, N.,Woolfson, D.N.,Savery, N.J.
Design and Selection of Heterodimerizing Helical Hairpins for Synthetic Biology.
Acs Synth Biol, 12:1845-1858, 2023
Cited by
PubMed Abstract: Synthetic biology applications would benefit from protein modules of reduced complexity that function orthogonally to cellular components. As many subcellular processes depend on peptide-protein or protein-protein interactions, designed polypeptides that can bring together other proteins controllably are particularly useful. Thanks to established sequence-to-structure relationships, helical bundles provide good starting points for such designs. Typically, however, such designs are tested and function in cells is not guaranteed. Here, we describe the design, characterization, and application of helical hairpins that heterodimerize to form 4-helix bundles in cells. Starting from a rationally designed homodimer, we construct a library of helical hairpins and identify complementary pairs using bimolecular fluorescence complementation in . We characterize some of the pairs using biophysics and X-ray crystallography to confirm heterodimeric 4-helix bundles. Finally, we demonstrate the function of an exemplar pair in regulating transcription in both and mammalian cells.
PubMed: 37224449
DOI: 10.1021/acssynbio.3c00231
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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