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PMID: 7481798 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Review

Protein design: a hierarchic approach.

Science (New York, N.Y.) ·Vol. 270 ·No. 5238 ·1995-11-10 ·Pages 935-41

Bryson JW, Betz SF, Lu HS, Suich DJ, Zhou HX, O'Neil KT, DeGrado WF

Abstract

The de novo design of peptides and proteins has recently emerged as an approach for investigating protein structure and function. Designed, helical peptides provide model systems for dissecting and quantifying the multiple interactions that stabilize secondary structure formation. De novo design is also useful for exploring the features that specify the stoichiometry and stability of alpha-helical coiled coils and for defining the requirements for folding into structures that resemble native, functional proteins. The design process often occurs in a series of discrete steps. Such steps reflect the hierarchy of forces required for stabilizing tertiary structures, beginning with hydrophobic forces and adding more specific interactions as required to achieve a unique, functional protein.

MeSH Terms
Amino Acid Sequence Crystallography, X-Ray DNA-Binding Proteins/chemistry Hydrogen Bonding Models, Molecular Molecular Sequence Data Protein Conformation Protein Engineering Protein Folding Protein Structure, Secondary Protein Structure, Tertiary Thermodynamics Zinc Fingers
Chemicals
DNA-Binding Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Bryson J W
DuPont Merck Pharmaceutical Company, Wilmington, DE 19880, USA.
Betz S F
Lu H S
Suich D J
Zhou H X
O'Neil K T
DeGrado W F
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1995-11-10
Pages
935-41
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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