An efficient method for enzyme immobilization evidenced by atomic force microscopy

Protein Engineering, Design and Selection

Volumn 25, Issue 11, 2012, Pages 715-723

  Marcuello, C ^a   De Miguel, R ^a   Gomez Moreno C ^a   Martinez Julvez M ^a,b   Lostao, A ^a,c  

^a UNIVERSITY OF ZARAGOZA   (Spain)

^b CSIC   (Spain)

^c FUNDACIÓN ARAID   (Spain)

Author keywords

atomic force microscopy; enzyme; immobilization; molecular recognition; protein interaction

Indexed keywords

CYTOCHROME C; DRUG SCREENING; ENZYMATIC ASSAY; IMMOBILIZED PROTEINS; INTERACTION SITE; PROTEIN ANALYSIS; PROTEIN INTERACTION; PROTEIN LIGANDS; PROTEIN-PROTEIN INTERACTIONS; REDOX PARTNERS; REDUCTASE ACTIVITY; SINGLE MOLECULE FORCE SPECTROSCOPY; SINGLE-MOLECULE ANALYSIS; SURFACE-BASED; WILD TYPES;

ATOMIC FORCE MICROSCOPY; BIOSENSORS; ENZYMES; LIGANDS; MOLECULAR RECOGNITION; MOLECULES; MONOLAYERS; PROTEINS; QUALITY CONTROL; RADIOACTIVE WASTE VITRIFICATION;

ENZYME IMMOBILIZATION;

FERREDOXIN; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE;

ATOMIC FORCE MICROSCOPY; CONFERENCE PAPER; ENZYMATIC ASSAY; ENZYME ACTIVITY; ENZYME IMMOBILIZATION; ENZYME KINETICS; ENZYME LOCALIZATION; LIGAND BINDING; MOLECULAR RECOGNITION; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN PROTEIN INTERACTION; PROTEIN PURIFICATION; STEADY STATE;

ALUMINUM SILICATES; ANABAENA; BACTERIAL PROTEINS; ENZYME ASSAYS; ENZYMES, IMMOBILIZED; FERREDOXIN-NADP REDUCTASE; FERREDOXINS; MICROSCOPY, ATOMIC FORCE; PROTEIN INTERACTION MAPPING;

EID: 84868583574     PISSN: 17410126     EISSN: 17410134     Source Type: Journal    
DOI: 10.1093/protein/gzs086     Document Type: Conference Paper

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