Advantages of quantitative affinity chromatography for the analysis of solute interaction with membrane proteins

Journal of Biochemical and Biophysical Methods

Volumn 49, Issue 1-3, 2001, Pages 507-521

  Lundqvist, Andreas ^a   Lundahl, Per ^b  

^a ASTRAZENECA R AND D   (Sweden)

^b UPPSALA UNIVERSITY   (Sweden)

Author keywords

Adsorption; Entrapment; Immobilization; Membrane protein; Quantitative affinity chromatography; Solute membrane protein interaction

Indexed keywords

GLUCOSE TRANSPORTER; GLYCOPROTEIN P; MEMBRANE PROTEIN; NICOTINIC RECEPTOR; NUCLEOSIDE;

ADSORPTION; AFFINITY CHROMATOGRAPHY; ANALYTIC METHOD; ARTICLE; BINDING AFFINITY; BINDING SITE; CONTROLLED STUDY; ERYTHROCYTE; GLUCOSE TRANSPORT; HUMAN; HUMAN CELL; MEMBRANE VESICLE; NONHUMAN; NUCLEOSIDE TRANSPORT; PHOTOSYNTHESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN IMMOBILIZATION; PROTEIN PROTEIN INTERACTION; PROTEOLIPOSOME; RHODOBACTER SPHAEROIDES;

ANIMALS; BRAIN; CARRIER PROTEINS; CHROMATOGRAPHY, AFFINITY; ERYTHROCYTES; GLUCOSE TRANSPORTER TYPE 1; HUMANS; MEMBRANE PROTEINS; MONOSACCHARIDE TRANSPORT PROTEINS; PHOTOSYNTHETIC REACTION CENTER COMPLEX PROTEINS; RATS; RECEPTORS, NICOTINIC; RECOMBINANT PROTEINS; SOLUTIONS;

RHODOBACTER SPHAEROIDES;

EID: 0035975899     PISSN: 0165022X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-022X(01)00192-0     Document Type: Article

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