Skip to main navigation Skip to search Skip to main content

The protein folding problem

  • Ken A. Dill
  • , S. Banu Ozkan
  • , M. Scott Shell
  • , Thomas R. Weikl
  • Arizona State University
  • University of California at Santa Barbara
  • Max Planck Institute of Colloids and Interfaces

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

932 Scopus citations

Abstract

The "protein folding problem" consists of three closely related puzzles: (a) What is the folding code? (b) What is the folding mechanism? (c) Can we predict the native structure of a protein from its amino acid sequence? Once regarded as a grand challenge, protein folding has seen great progress in recent years. Now, foldable proteins and nonbiological polymers are being designed routinely and moving toward successful applications. The structures of small proteins are now often well predicted by computer methods. And, there is now a testable explanation for how a protein can fold so quickly: A protein solves its large global optimization problem as a series of smaller local optimization problems, growing and assembling the native structure from peptide fragments, local structures first.

Original languageEnglish
Title of host publicationAnnual Review of Biophysics
Pages289-316
Number of pages28
DOIs
StatePublished - 2008

Publication series

NameAnnual Review of Biophysics
Volume37

Keywords

  • CASP
  • Folding code
  • Folding kinetics
  • Funnel energy landscapes
  • Structure prediction

Fingerprint

Dive into the research topics of 'The protein folding problem'. Together they form a unique fingerprint.

Cite this