Abstract
We present an integrated approach for efficient characterization of intrinsically disordered proteins. Batch cell-free expression, fast data acquisition, automated analysis, and statistical validation with data resampling have been combined for achieving cost-effective protein expression, and rapid automated backbone assignment. The new methodology is applied for characterization of five cytosolic domains from T- and B-cell receptors in solution.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Amino Acid Motifs
-
Cytosol / metabolism
-
Humans
-
Intracellular Space / metabolism
-
Intrinsically Disordered Proteins / chemistry*
-
Intrinsically Disordered Proteins / metabolism
-
Ligands
-
Nuclear Magnetic Resonance, Biomolecular / methods*
-
Protein Structure, Tertiary
-
Receptors, Antigen, B-Cell / chemistry*
-
Receptors, Antigen, B-Cell / metabolism
-
Receptors, Antigen, T-Cell / chemistry*
-
Receptors, Antigen, T-Cell / metabolism
-
Signal Transduction
Substances
-
Intrinsically Disordered Proteins
-
Ligands
-
Receptors, Antigen, B-Cell
-
Receptors, Antigen, T-Cell