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7FBA

De Novo-Designed and Disulfide-Bridged Peptide Heterodimer - hd2

Summary for 7FBA
Entry DOI10.2210/pdb7fba/pdb
DescriptorGLU-CYS-ARG-GLU-TYR-GLY-PRO-LE1-LYS-LE1-LE1-ALA-NH2, ALA-LE1-CYS-GLU-CYS-GLY-PRO-THR-ARG-GLU-CYS-LYS-NH2 (2 entities in total)
Functional Keywordsde novo design, disulfide-bridged peptide, heterodimer, penicillamine, de novo protein
Biological sourceEscherichia virus M13
More
Total number of polymer chains2
Total formula weight2773.37
Authors
Yao, H.,Yao, S.,Moyer, A.,Zheng, Y.,Baker, D.,Wu, C. (deposition date: 2021-07-08, release date: 2022-05-18, Last modification date: 2023-11-15)
Primary citationYao, S.,Moyer, A.,Zheng, Y.,Shen, Y.,Meng, X.,Yuan, C.,Zhao, Y.,Yao, H.,Baker, D.,Wu, C.
De novo design and directed folding of disulfide-bridged peptide heterodimers.
Nat Commun, 13:1539-1539, 2022
Cited by
PubMed Abstract: Peptide heterodimers are prevalent in nature, which are not only functional macromolecules but molecular tools for chemical and synthetic biology. Computational methods have also been developed to design heterodimers of advanced functions. However, these peptide heterodimers are usually formed through noncovalent interactions, which are prone to dissociate and subject to concentration-dependent nonspecific aggregation. Heterodimers crosslinked with interchain disulfide bonds are more stable, but it represents a formidable challenge for both the computational design of heterodimers and the manipulation of disulfide pairing for heterodimer synthesis and applications. Here, we report the design, synthesis and application of interchain disulfide-bridged peptide heterodimers with mutual orthogonality by combining computational de novo designs with a directed disulfide pairing strategy. These heterodimers can be used as not only scaffolds for generating functional molecules but chemical tools or building blocks for protein labeling and construction of crosslinking hybrids. This study thus opens the door for using this unexplored dimeric structure space for many biological applications.
PubMed: 35318337
DOI: 10.1038/s41467-022-29210-x
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

226707

數據於2024-10-30公開中

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