A synergistic approach to protein crystallization: combination of a fixed-arm carrier with surface entropy reduction

Protein Sci. 2010 May;19(5):901-13. doi: 10.1002/pro.368.

Abstract

Protein crystallographers are often confronted with recalcitrant proteins not readily crystallizable, or which crystallize in problematic forms. A variety of techniques have been used to surmount such obstacles: crystallization using carrier proteins or antibody complexes, chemical modification, surface entropy reduction, proteolytic digestion, and additive screening. Here we present a synergistic approach for successful crystallization of proteins that do not form diffraction quality crystals using conventional methods. This approach combines favorable aspects of carrier-driven crystallization with surface entropy reduction. We have generated a series of maltose binding protein (MBP) fusion constructs containing different surface mutations designed to reduce surface entropy and encourage crystal lattice formation. The MBP advantageously increases protein expression and solubility, and provides a streamlined purification protocol. Using this technique, we have successfully solved the structures of three unrelated proteins that were previously unattainable. This crystallization technique represents a valuable rescue strategy for protein structure solution when conventional methods fail.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antigens, Dermatophagoides / biosynthesis
  • Antigens, Dermatophagoides / chemistry
  • Antigens, Dermatophagoides / genetics
  • Arabidopsis
  • Arabidopsis Proteins / biosynthesis
  • Arabidopsis Proteins / chemistry
  • Arabidopsis Proteins / genetics
  • Arthropod Proteins
  • Base Sequence
  • Chickens
  • Crystallization / methods*
  • Crystallography, X-Ray
  • Dermatophagoides pteronyssinus
  • Entropy
  • Maltose-Binding Proteins
  • Models, Molecular
  • Molecular Sequence Data
  • Periplasmic Binding Proteins / biosynthesis
  • Periplasmic Binding Proteins / chemistry*
  • Periplasmic Binding Proteins / genetics
  • Protein Conformation
  • Receptors for Activated C Kinase
  • Receptors, Cell Surface / biosynthesis
  • Receptors, Cell Surface / chemistry
  • Receptors, Cell Surface / genetics
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / chemistry*
  • Recombinant Fusion Proteins / genetics
  • Sulfotransferases / biosynthesis
  • Sulfotransferases / chemistry
  • Sulfotransferases / genetics

Substances

  • Antigens, Dermatophagoides
  • Arabidopsis Proteins
  • Arthropod Proteins
  • Dermatophagoides pteronyssinus antigen p 7
  • Maltose-Binding Proteins
  • Periplasmic Binding Proteins
  • RACK1 protein, Arabidopsis
  • Receptors for Activated C Kinase
  • Receptors, Cell Surface
  • Recombinant Fusion Proteins
  • Sulfotransferases