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O Diettrich

Publications and source records attributed to O Diettrich.

3 recordsLinked to original sources

Application of magnetic chromatography to the isolation of lysosomes from fibroblasts of patients with lysosomal storage disorders.

A method for the purification of lysosomes from fibroblasts has been developed which uses endocytosis of superparamagnetic colloidal iron dextran particles followed by separation of the iron-containing lysosomes in a magnetic field. This permitted isolation of lysosomes from fibroblasts from patients with infantile sialic acid storage disorder and other lysosomal storage diseases in which a shift in lysosomal density induced by the storage material prevents purification by centrifugation in a Percoll gradient. The magnetic lysosomes isolated from these cells are very similar to those from normal cells as judged by lysosomal marker enzyme activity and 2D-PAGE analysis of the enriched proteins.

Cell Fractionation↗

Purification of lysosomal membrane proteins from human placenta.

A major portion of the intracellular hydrolytic reactions are confined to lysosomes, whose membrane proteins take care of the proper lumenal milieu and the release of the degradation products. To obtain material for structural characterization of the transport proteins, we elaborated a procedure for isolation of lysosomal membranes and separation of their proteins in a two-dimensional electrophoresis. In a first step dense lysosomes were isolated from human placenta using a Percoll gradient. Subsequently, lysosomal membranes were purified by immunoadsorption. The procedure yielded mg-amounts of lysosomal membranes. Proteins associated with lysosomal membranes, acid beta-glucosidase, acetyl-coenzyme A:alpha-glucosaminide N-acetyltransferase, CD63/LIMP I, and h-lamp-2 were enriched approximately 300-fold as compared to the initial homogenate. Separation of the membrane proteins was achieved in a two-dimensional electrophoresis. The procedure is expected to yield material for structural studies on lysosomal membrane proteins with suspected defects in lysosomal storage diseases.

Cells, Cultured↗

Two-way adaptors.

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Adaptation, Physiological↗