Analytical Approaches in Cell Biology：在细胞生物学中的分析方法.pptVIP

Analytical Approaches in Cell Biology * BSCI 420 Sept 12, 2002 “Make everything as simple as possible, but not simpler” -Albert Einstein 1. Separation of cell components 2. Cell culture, fusion and hybridomas 1. Separatory techniques: Cells must first be disrupted by homogenization, osmotic rupture, detergent lysis, or ultrasonic disruption. A. Centrifugation is useful for separation on the basis of mass or density. [A8-7] preparative ultracentrifuge 1) Differential acceleration: Repeated centrifugation at progressively higher speeds, e.g. low 1000 X g med 20,000 X g high 80,000 X g very high 150,000 X g Preparative ultracentrifuge Differential acceleration Velocity sedimentation Equilibrium density- gradient centrifugation To sep. organelles or molecules of similar mass but diff. Densities. E.g., lysosomes mitoch. Or labeled DNA from inlabeled. 2. Chromatography A) Ion exchange - Charged resin on beads, e.g. DEAE dextran (+) 0r phosphocellulose (-) charged. Oppositely charged molecules bind, released by salt solution. B) Gel filtration - Retards smaller molecules that enter pores in gel beads, so larger molecules come thru 1st. C) Affinity chromatography - Specific ligand or antibody bound to beads. Elute with buffer that dissociates ligand from protein, e.g. low pH, hi salt 3. Electrophoresis Separates based on migration rate in electrical field. Most common: SDSUniformly neg charged so migrate on the basis of size Isoelectric focusing; Run in solution of ampholines that maintain a pH gradient *