Engineering of recombinant human Fcγ receptor i by directed evolution

Protein Engineering, Design and Selection

Volumn 25, Issue 12, 2012, Pages 835-842

  Asaoka, Yoshiharu ^a,c   Hatayama, Kouta ^b   Tsumoto, Kanta ^c   Tomita, Masahiro ^c   Ide, Teruhiko ^a,b  

^a TOSOH CORPORATION   (Japan)

^b SAGAMI CHEMICAL RESEARCH CENTER   (Japan)

^c MIE UNIVERSITY   (Japan)

Author keywords

CD64; directed evolution; Fc RI; random mutagenesis; thermal stability

Indexed keywords

BINDING ACTIVITIES; BINDING AFFINITIES; CD64; DIRECTED EVOLUTION; EQUILIBRIUM DISSOCIATION CONSTANT; HUMAN IGG; PRODUCTION RATES; RANDOM MUTAGENESIS; TRANSITION MIDPOINT; WILD TYPES;

AFFINITY CHROMATOGRAPHY; AMINO ACIDS; BINDING ENERGY; DIAGNOSIS; DISSOCIATION; ESCHERICHIA COLI; MUTAGENESIS;

THERMODYNAMIC STABILITY;

AMINO ACID; FC RECEPTOR; IMMUNOGLOBULIN G; RECOMBINANT RECEPTOR;

ARTICLE; BINDING AFFINITY; DISSOCIATION CONSTANT; ESCHERICHIA COLI; GENE EXPRESSION; GENE MUTATION; MUTAGENESIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ENGINEERING; SCREENING; THERMOSTABILITY; WILD TYPE;

AMINO ACID SEQUENCE; BINDING SITES; DIRECTED MOLECULAR EVOLUTION; ESCHERICHIA COLI; HUMANS; KINETICS; MUTAGENESIS, SITE-DIRECTED; PROTEIN ENGINEERING; PROTEIN STABILITY; RECEPTORS, IGG; RECOMBINANT PROTEINS; SURFACE PLASMON RESONANCE;

ESCHERICHIA COLI;

EID: 84870231029     PISSN: 17410126     EISSN: 17410134     Source Type: Journal    
DOI: 10.1093/protein/gzs053     Document Type: Article

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