The overall goal of the proposed research is to design and produce libraries of de novo proteins that fold into well ordered alpha-helical structures. This goal will be pursued through an approach that uses both rational design and combinatorial methods. The first step will entail the design of a new structural scaffold specifying a uniquely folded 4-helix bundle. Each sequence position will be defined to occur in a particular environment in the desired alpha-helical structure (exposed vs. buried; alpha-helix vs. turn etc.). The second step will use combinatorial methods to generate a library of de novo amino acid sequences consistent with the designed scaffold. The combinatorial diversity will not be random, but instead, will be designed to deliver at each position only those amino acids most compatible with the structural environment of that position in the scaffold.
The specific aims of this project are (1) to design a new structural scaffold that specifies a 4-helix bundle; (2) to design and construct a library of synthetic genes that encode a large collection of protein sequences consistent with this new scaffold; (3) to express and purify de novo proteins from this collection; (4) to biophysically characterize the structural and thermodynamic properties of the purified proteins and thereby assess whether they form molten globule ensembles or uniquely folded structures; and (5) to determine the 3-dimensional structures of representative proteins by NMR spectroscopy. The ability to design and construct large collections of uniquely folded de novo proteins will have a significant impact on biotechnology and medicine. Whereas current applications of biotechnology typically focus on the control, modification, and production of naturally occurring genes and proteins, future applications will not be limited to macromolecules provided by nature. The ability to produce libraries of well folded de novo proteins is an initial and essential step towards the ultimate goal of discovering novel proteins """"""""tailor made"""""""" for applications in industry and medicine.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM062869-02
Application #
6520444
Study Section
Molecular and Cellular Biophysics Study Section (BBCA)
Program Officer
Li, Jerry
Project Start
2001-04-01
Project End
2005-03-31
Budget Start
2002-04-01
Budget End
2003-03-31
Support Year
2
Fiscal Year
2002
Total Cost
$233,769
Indirect Cost
Name
Princeton University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
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Das, Aditi; Wei, Yinan; Pelczer, Istvan et al. (2011) Binding of small molecules to cavity forming mutants of a de novo designed protein. Protein Sci 20:702-11
Das, Aditi; Hecht, Michael H (2007) Peroxidase activity of de novo heme proteins immobilized on electrodes. J Inorg Biochem 101:1820-6
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Bradley, Luke H; Thumfort, Peter P; Hecht, Michael H (2006) De novo proteins from binary-patterned combinatorial libraries. Methods Mol Biol 340:53-69
Bradley, Luke H; Kleiner, Ralph E; Wang, Anna F et al. (2005) An intein-based genetic selection allows the construction of a high-quality library of binary patterned de novo protein sequences. Protein Eng Des Sel 18:201-7
Klepeis, John L; Wei, Yinan; Hecht, Michael H et al. (2005) Ab initio prediction of the three-dimensional structure of a de novo designed protein: a double-blind case study. Proteins 58:560-70
Hu, Ying; Das, Aditi; Hecht, Michael H et al. (2005) Nanografting de novo proteins onto gold surfaces. Langmuir 21:9103-9
Hecht, Michael H; Das, Aditi; Go, Abigail et al. (2004) De novo proteins from designed combinatorial libraries. Protein Sci 13:1711-23
Wei, Yinan; Hecht, Michael H (2004) Enzyme-like proteins from an unselected library of designed amino acid sequences. Protein Eng Des Sel 17:67-75

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