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8GIV

Porous framework formed by assembly of a bipyridyl-conjugated helical peptide

Summary for 8GIV
Entry DOI10.2210/pdb8giv/pdb
Descriptorbipyridyl-conjugated helical peptide (2 entities in total)
Functional Keywordsde novo protein
Biological sourcesynthetic construct
Total number of polymer chains2
Total formula weight2516.98
Authors
Hess, S.S.,Nguyen, A.I. (deposition date: 2023-03-14, release date: 2023-11-15, Last modification date: 2024-09-25)
Primary citationHess, S.S.,Coppola, F.,Dang, V.T.,Tran, P.N.,Mickel, P.J.,Oktawiec, J.,Ren, Z.,Kral, P.,Nguyen, A.I.
Noncovalent Peptide Assembly Enables Crystalline, Permutable, and Reactive Thiol Frameworks.
J.Am.Chem.Soc., 145:19588-19600, 2023
Cited by
PubMed Abstract: Though thiols are exceptionally versatile, their high reactivity has also hindered the synthesis and characterization of well-defined thiol-containing porous materials. Leveraging the mild conditions of the noncovalent peptide assembly, we readily synthesized and characterized a number of frameworks with thiols displayed at many unique positions and in several permutations. Importantly, nearly all assemblies were structurally determined using single-crystal X-ray diffraction to reveal their rich sequence-structure landscape and the cooperative noncovalent interactions underlying their assembly. These observations and supporting molecular dynamics calculations enabled rational engineering by the positive and negative design of noncovalent interactions. Furthermore, the thiol-containing frameworks undergo diverse single-crystal-to-single-crystal reactions, including toxic metal ion coordination (e.g., Cd, Pb, and Hg), selective uptake of Hg ions, and redox transformations. Notably, we find a framework that supports thiol-nitrosothiol interconversion, which is applicable for biocompatible nitric oxide delivery. The modularity, ease of synthesis, functionality, and well-defined nature of these peptide-based thiol frameworks are expected to accelerate the design of complex materials with reactive active sites.
PubMed: 37639365
DOI: 10.1021/jacs.3c03645
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (0.99 Å)
Structure validation

226707

건을2024-10-30부터공개중

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