Concentrating Proteins by Salt, Polyethylene Glycol, Solvent, SDS Precipitation, Three-Phase Partitioning, Dialysis, Centrifugation, Ultrafiltration, Lyophilization, Affinity Chromatography, Immunoprecipitation or Increased Temperature for Protein Isolation, Drug Interaction, and Proteomic and Peptidomic Evaluation.

J P Dean Goldring
Author Information
  1. J P Dean Goldring: Department of Biochemistry, University of KwaZulu-Natal, Scottsville, South Africa. Goldringd@ukzn.ac.za.

Abstract

In protein isolation, drug interaction studies, and proteomic or peptidomic procedures, protein solutions are often concentrated to remove solvents and undesirable molecules, to separate protein fractions, or to increase protein concentrations. Proteins can be concentrated by precipitation from solution with ammonium sulfate, polyethylene glycol, organic solvents, trichloroacetic acid, potassium chloride/sodium dodecyl sulfate thermal denaturation, and three-phase partitioning. Solvents can be removed by passage through a semipermeable barrier where protein solutions are forced against the barrier in a centrifuge tube or with increased pressure, concentrating proteins in the remaining solution. The semipermeable barrier can be surrounded by a hygroscopic reagent to draw the solvent across the membrane. Proteins can be concentrated by freeze-drying (lyophilization). Unique ligand interactions with proteins can be used to select for proteins by affinity purification or immunoprecipitation. All these methods to concentrate proteins are discussed.

Keywords

MeSH Term

Chromatography, Affinity
Drug Interactions
Freeze Drying
Immunoprecipitation
Peptides
Polyethylene Glycols
Proteins
Proteomics
Sodium Dodecyl Sulfate
Ultrafiltration

Chemicals

Peptides
Proteins
Sodium Dodecyl Sulfate
Polyethylene Glycols
dodecyl sulfate

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