De NovoDesign of Helical Bundles as Models for Understanding Protein Folding and Function
- 24 October 2000
- journal article
- review article
- Published by American Chemical Society (ACS) in Accounts of Chemical Research
- Vol. 33 (11) , 745-754
- https://doi.org/10.1021/ar970004h
Abstract
De novo protein design has proven to be a powerful tool for understanding protein folding, structure, and function. In this Account, we highlight aspects of our research on the design of dimeric, four-helix bundles. Dimeric, four-helix bundles are found throughout nature, and the history of their design in our laboratory illustrates our hierarchic approach to protein design. This approach has been successfully applied to create a completely native-like protein. Structural and mutational analysis allowed us to explore the determinants of native protein structure. These determinants were then applied to the design of a dinuclear metal-binding protein that can now serve as a model for this important class of proteins.Keywords
This publication has 113 references indexed in Scilit:
- Defining the core structure of the α-lactalbumin molten globule state 1 1Edited by C. R. MatthewsJournal of Molecular Biology, 1999
- Using loop length variants to dissect the folding pathway of a four-helix-bundle proteinJournal of Molecular Biology, 1999
- De Novo Design of Protein Function: Predictable Structure−Function Relationships in Synthetic Redox ProteinsJournal of the American Chemical Society, 1999
- Design of peptides undergoing self-catalytic α-to-β transition and amyloidogenesisBiopolymers, 1998
- De Novo protein design: towards fully automated sequence selection 1 1Edited by P. E. WrightJournal of Molecular Biology, 1997
- Rotamers: To be or not to be?Journal of Molecular Biology, 1993
- Backbone-dependent Rotamer Library for Proteins Application to Side-chain PredictionJournal of Molecular Biology, 1993
- The role of internal packing interactions in determining the structure and stability of a proteinJournal of Molecular Biology, 1991
- Chemical and mutagenic analysis of aminomethylphosphonate biodegradationJournal of the American Chemical Society, 1987
- How different amino acid sequences determine similar protein structures: The structure and evolutionary dynamics of the globinsJournal of Molecular Biology, 1980