Characterization of an FcγRI-binding peptide selected by phage display

Protein Engineering, Design and Selection

Volumn 19, Issue 3, 2006, Pages 121-128

  Berntzen, G ^a   Brekke, O H ^b   Mousavi, S A ^a   Andersen, J T ^a   Michaelsen, T E ^c   Berg, T ^a   Sandlie, I ^a   Lauvrak, V ^a,d  

^a UNIVERSITY OF OSLO   (Norway)

^b Dynal Biotech ASA   (Norway)

^c NORWEGIAN INSTITUTE OF PUBLIC HEALTH   (Norway)

^d AKERSHUS UNIVERSITY HOSPITAL   (Norway)

Author keywords

Cell internalization; Fc receptors; Peptide selection; Phage display; U937 cells

Indexed keywords

ANTIBODIES; ANTIGENS; CELLS; MOLECULAR DYNAMICS; VACCINES;

CELL INTERNALIZATION; FCΓ RECEPTORS; PEPTIDE SELECTION; PHAGE DISPLAY; U937 CELLS;

AMINO ACIDS;

BINDING PROTEIN; BIOTIN; FC RECEPTOR; GAMMA INTERFERON; IMMUNOGLOBULIN G; MONOCLONAL ANTIBODY; MONOCLONAL ANTIBODY 22; MONOCLONAL ANTIBODY 32.2; PEPTIDE LIBRARY; REAGENT; RECEPTOR SUBTYPE; STREPTAVIDIN; UNCLASSIFIED DRUG; FCGR1A PROTEIN, HUMAN; FLUORESCEIN ISOTHIOCYANATE; FLUORESCENT DYE; PEPTIDE;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CONJUGATION; CONTROLLED STUDY; FLOW CYTOMETRY; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; INTERNALIZATION; MAGNETISM; MONOCYTE; MOUSE; NONHUMAN; PHAGE DISPLAY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN DOMAIN; RECEPTOR BINDING; SOLUBILITY; CELL STRAIN U937; FLUORESCENT ANTIBODY TECHNIQUE; GENETICS; IMMUNOLOGY; ISOLATION AND PURIFICATION; METABOLISM;

ANIMALIA;

ANTIBODIES, MONOCLONAL; FLOW CYTOMETRY; FLUORESCEIN-5-ISOTHIOCYANATE; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; FLUORESCENT DYES; HUMANS; IMMUNOGLOBULIN G; INTERFERON TYPE II; PEPTIDE LIBRARY; PEPTIDES; RECEPTORS, IGG; U937 CELLS;

EID: 33644975667     PISSN: 17410126     EISSN: 17410134     Source Type: Journal    
DOI: 10.1093/protein/gzj011     Document Type: Article

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