Literature DB >> 7481798

Protein design: a hierarchic approach.

J W Bryson1, S F Betz, H S Lu, D J Suich, H X Zhou, K T O'Neil, W F DeGrado.   

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.

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Year:  1995        PMID: 7481798     DOI: 10.1126/science.270.5238.935

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  107 in total

1.  Conversion of a maltose receptor into a zinc biosensor by computational design.

Authors:  J S Marvin; H W Hellinga
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-24       Impact factor: 11.205

2.  A designed four-alpha-helix bundle that binds the volatile general anesthetic halothane with high affinity.

Authors:  J S Johansson; D Scharf; L A Davies; K S Reddy; R G Eckenhoff
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

3.  Contribution of proton linkage to the thermodynamic stability of the major cold-shock protein of Escherichia coli CspA.

Authors:  S A Petrosian; G I Makhatadze
Journal:  Protein Sci       Date:  2000-02       Impact factor: 6.725

4.  Synthesis and NMR solution structure of an alpha-helical hairpin stapled with two disulfide bridges.

Authors:  P Barthe; S Rochette; C Vita; C Roumestand
Journal:  Protein Sci       Date:  2000-05       Impact factor: 6.725

5.  A polar, solvent-exposed residue can be essential for native protein structure.

Authors:  R B Hill; W F DeGrado
Journal:  Structure       Date:  2000-05-15       Impact factor: 5.006

6.  Rational design of nascent metalloenzymes.

Authors:  D E Benson; M S Wisz; H W Hellinga
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

7.  Altering dimerization specificity by changes in surface electrostatics.

Authors:  M J Nohaile; Z S Hendsch; B Tidor; R T Sauer
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-27       Impact factor: 11.205

8.  Crystal structure of a designed, thermostable, heterotrimeric coiled coil.

Authors:  S Nautiyal; T Alber
Journal:  Protein Sci       Date:  1999-01       Impact factor: 6.725

Review 9.  De novo design of helical bundles as models for understanding protein folding and function.

Authors:  R B Hill; D P Raleigh; A Lombardi; W F DeGrado
Journal:  Acc Chem Res       Date:  2000-11       Impact factor: 22.384

10.  Understanding the sequence determinants of conformational switching using protein design.

Authors:  S Dalal; L Regan
Journal:  Protein Sci       Date:  2000-09       Impact factor: 6.725

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