The isolation of large quantities of undamaged cellular organelles and cytosolic enzymes using a low-shear continuous tissue homogenizer

Thomas C. Spelsberg, Gregory D. Reinhart, Steve Barham

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

There is often a need to isolate large quantities of subcellular components such as membrane-coated organelles (e.g., nuclei, lysosomes, and mitochondria), cell membranes, and soluble (cytosolic) proteins. Instruments which can homogenize relatively large masses of tissue, primarily those with rapidly rotating blades and cylinders, are excessively vigorous, often resulting in damaged and/or low yields of the subcellular components. This paper describes procedures for obtaining high yields of undamaged subcellular components using a continuous bulk tissue homogenizer which performs with low shear (the low-shear continuous homogenizer or LSC). This homogenizer is simple in operation, durable and can be used with a variety of tissues. Fibrous tissues are more difficult to homogenize using this instrumentation and require a premincing to small pieces (0.2 to 1.0-cm diam) followed by filtration through 2-4 mesh (two to four apertures per inch). Methods for bulk preparations with enhanced recoveries of undamaged nuclei, and a typical soluble multimeric enzyme, phosphofructokinase, are presented. Electron microscope views of the homogenates show the preserved state of the other subcellular components. The LSC homogenizer requires less physical effort with no "hands on" operation and thus is safer. This homogenizer requires less homogenization time compared to the smaller, hand-held Potter-Elvehjem-type homogenizers. Operations requiring low temperature can be performed at room temperature as long as the continuously passing homogenate solutions are kept chilled.

Original languageEnglish (US)
Pages (from-to)237-248
Number of pages12
JournalAnalytical Biochemistry
Volume143
Issue number2
DOIs
StatePublished - 1984

Fingerprint

Organelles
Tissue
Enzymes
Hand
Enhanced recovery
Low temperature operations
Physical Exertion
Phosphofructokinases
Mitochondria
Temperature
Cell membranes
Lysosomes
Electron microscopes
Cell Membrane
Electrons
Membranes
Proteins

Keywords

  • bulk isolation
  • continuous homogenizer
  • electron microscopy
  • enzymes
  • nuclei
  • organelles

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Molecular Biology

Cite this

The isolation of large quantities of undamaged cellular organelles and cytosolic enzymes using a low-shear continuous tissue homogenizer. / Spelsberg, Thomas C.; Reinhart, Gregory D.; Barham, Steve.

In: Analytical Biochemistry, Vol. 143, No. 2, 1984, p. 237-248.

Research output: Contribution to journalArticle

Spelsberg, Thomas C. ; Reinhart, Gregory D. ; Barham, Steve. / The isolation of large quantities of undamaged cellular organelles and cytosolic enzymes using a low-shear continuous tissue homogenizer. In: Analytical Biochemistry. 1984 ; Vol. 143, No. 2. pp. 237-248.
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