Design of metal-mediated protein assemblies via hydroxamic acid functionalities
Autor: | Jerika A. Chiong, F. Akif Tezcan, Yiying Li, Rohit H. Subramanian, Jie Zhu, Jake B. Bailey, Eyal Golub |
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Rok vydání: | 2021 |
Předmět: |
Models
Molecular Hydroxamic Acids Ligands General Biochemistry Genetics and Molecular Biology law.invention Metal 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine law Molecule Cysteine Crystallization Metal-Organic Frameworks 030304 developmental biology 0303 health sciences Hydroxamic acid Ligand Proteins Combinatorial chemistry Monomer chemistry Metals Transmission electron microscopy Area Under Curve visual_art Ferritins visual_art.visual_art_medium 030217 neurology & neurosurgery Conjugate |
Zdroj: | Nature Protocols. 16:3264-3297 |
ISSN: | 1750-2799 1754-2189 |
DOI: | 10.1038/s41596-021-00535-z |
Popis: | The self-assembly of proteins into sophisticated multicomponent assemblies is a hallmark of all living systems and has spawned extensive efforts in the construction of novel synthetic protein architectures with emergent functional properties. Protein assemblies in nature are formed via selective association of multiple protein surfaces through intricate noncovalent protein-protein interactions, a challenging task to accurately replicate in the de novo design of multiprotein systems. In this protocol, we describe the application of metal-coordinating hydroxamate (HA) motifs to direct the metal-mediated assembly of polyhedral protein architectures and 3D crystalline protein-metal-organic frameworks (protein-MOFs). This strategy has been implemented using an asymmetric cytochrome cb562 monomer through selective, concurrent association of Fe3+ and Zn2+ ions to form polyhedral cages. Furthermore, the use of ditopic HA linkers as bridging ligands with metal-binding protein nodes has allowed the construction of crystalline 3D protein-MOF lattices. The protocol is divided into two major sections: (1) the development of a Cys-reactive HA molecule for protein derivatization and self-assembly of protein-HA conjugates into polyhedral cages and (2) the synthesis of ditopic HA bridging ligands for the construction of ferritin-based protein-MOFs using symmetric metal-binding protein nodes. Protein cages are analyzed using analytical ultracentrifugation, transmission electron microscopy and single-crystal X-ray diffraction techniques. HA-mediated protein-MOFs are formed in sitting-drop vapor diffusion crystallization trays and are probed via single-crystal X-ray diffraction and multi-crystal small-angle X-ray scattering measurements. Ligand synthesis, construction of HA-mediated assemblies, and post-assembly analysis as described in this protocol can be performed by a graduate-level researcher within 6 weeks. |
Databáze: | OpenAIRE |
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