De Novo Design of a Single Chain Diphenylporphyrin Metalloprotein

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Amino Acid Sequence
Chromatography, Gel
Circular Dichroism
Metalloproteins
Models, Molecular
Molecular Sequence Data
Nuclear Magnetic Resonance, Biomolecular
Porphyrins
Protein Structure, Secondary
Spectrophotometry, Ultraviolet
Thermodynamics
Ultracentrifugation
Amino Acid Sequence
Chromatography
Gel
Circular Dichroism
Metalloproteins
Models
Molecular
Molecular Sequence Data
Nuclear Magnetic Resonance
Biomolecular
Porphyrins
Protein Structure
Secondary
Spectrophotometry
Ultraviolet
Thermodynamics
Ultracentrifugation
Biochemistry
Organic Chemistry

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Bender, Gretchen M
Lehmann, Andreas
Zou, Hongling
Cheng, Hong
Fry, H Christopher
Engel, Don
Therien, Michael J
Blasie, J Kent
Roder, Heinrich

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Abstract

We describe the computational design of a single-chain four-helix bundle that noncovalently self-assembles with fully synthetic non-natural porphyrin cofactors. With this strategy, both the electronic structure of the cofactor as well as its protein environment may be varied to explore and modulate the functional and photophysical properties of the assembly. Solution characterization (NMR, UV-vis) of the protein showed that it bound with high specificity to the desired cofactors, suggesting that a uniquely structured protein and well-defined site had indeed been created. This provides a genetically expressed single-chain protein scaffold that will allow highly facile, flexible, and asymmetric variations to enable selective incorporation of different cofactors, surface-immobilization, and introduction of spectroscopic probes.

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2007-09-05

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Journal of the American Chemical Society

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