Efficient phage display of intracellularly folded proteins mediated by the TAT pathway

Protein Engineering, Design and Selection

Volumn 24, Issue 6, 2011, Pages 473-484

  Speck, Janina ^a   Arndt, Katja M ^a,b   Mller, Kristian M ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY OF POTSDAM   (Germany)

Author keywords

g3p; phagemid display; protein design; protein engineering; selection

Indexed keywords

G3P; PHAGEMID DISPLAY; PROTEIN DESIGN; PROTEIN ENGINEERING; SELECTION;

AMINO ACIDS; DISPLAY DEVICES; FLUORESCENCE; GENETIC ENGINEERING; OLIGOMERIZATION; OLIGOMERS; PLANTS (BOTANY); SIGNAL PROCESSING;

PROTEINS;

ARGININE; ARGONAUTE PROTEIN; CYSTEINE; DSBA PROTEIN; GREEN FLUORESCENT PROTEIN; LUCIFERASE; MONOMER; PELB PROTEIN; RED FLUORESCENT PROTEIN; SIGNAL PEPTIDE; SIGNAL RECOGNITION PARTICLE; TORA PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; ARTICLE; CYTOPLASM; CYTOSOL; GENE; MOLECULAR WEIGHT; OLIGOMERIZATION; PHAGE DISPLAY; PHAGEMID; PRIORITY JOURNAL; PROTEIN FOLDING; PROTEIN FUNCTION; PURIFICATION;

BACTERIOPHAGES; CELL SURVIVAL; CLONING, MOLECULAR; ENDORIBONUCLEASES; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; INTRACELLULAR SPACE; LUMINESCENT PROTEINS; MEMBRANE TRANSPORT PROTEINS; PEPTIDE LIBRARY; PLASMIDS; PROTEIN ENGINEERING; PROTEIN FOLDING; SECRETORY PATHWAY; SIGNAL RECOGNITION PARTICLE; TEMPERATURE;

EID: 79956126348     PISSN: 17410126     EISSN: 17410134     Source Type: Journal    
DOI: 10.1093/protein/gzr001     Document Type: Article

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