Cytology · MU Sofia

7. Cell fractionation. Histoautoradiography.

Covers cell fractionation: how homogenisation, filtration and repeated centrifugation separate organelles, the collection and analysis of fractions, and why isolating mitochondria is a common example. It then explains autoradiography, from introducing a radioactive label through silver bromide emulsion development to its uses in tracking DNA replication and protein synthesis. A brief section on X-ray crystallography, covering its procedure, applications and example molecules, closes the note.

Inside: 4 sections · 5 labelled pictures · 14 flashcards · 7 min

Topic 7 of 127 in the MU Sofia syllabus for Cytology (Dental Medicine, Year 1). The free AceMed note covers it in 4 sections, about 986 words (7 min of reading), with 14 flashcards.

In this note

  1. Introduction
  2. Notes on Autoradiography and X-Ray Crystallography
  3. Autoradiography
  4. X-Ray Crystallography

Introduction

Cell Fractionation

Cell fractionation is a valuable technique used to isolate and study individual organelles and cellular components from a heterogeneous mixture of cells. This method was developed in the 1940s and 1950s by Albert Claude, Christian de Duve, and George Palade.

Key Steps in Cell Fractionation

Cell fractionation typically involves the following steps:

Homogenization: Cells are disrupted and broken down to release their internal components. This is often done in an isotonic buffer to maintain the osmotic balance and prevent damage to the organelles.

This process is similar to the first step of isolating primary cells for cell culture, as mentioned in our previous conversation, where tissues are mechanically and enzymatically disrupted.

Filtration: The homogenate is filtered to remove any large debris, such as unbroken cells and connective tissue.

Centrifugation: The filtrate is subjected to repeated rounds of centrifugation at increasing speeds.

This process separates the cellular components based on their size, shape, and density.

Larger and denser components, such as nuclei, sediment at lower speeds, while smaller and less dense components, such as ribosomes, require higher speeds for sedimentation.

Collection of Fractions: The separated components, called fractions, are collected at each centrifugation step.

Analysis: The isolated fractions are analyzed to determine their composition and function.

Various techniques are used for this analysis, including microscopy, enzyme assays, Western blotting, and mass spectrometry.

Some of these techniques, such as microscopy and Western blotting, have been mentioned in our conversation history.

Purpose of Cell Fractionation

The primary purpose of cell fractionation is to separate organelles systematically for individual study. By isolating organelles, researchers can:

Study their structure and function in detail.

Investigate their biochemical properties.

Determine their protein and lipid composition.

Understand their roles in cellular processes.

Benefits of Cell Fractionation

Preservation of Organelle Function: The technique is designed to preserve the normal functioning of the organelles so they can be studied in a near-native state.

Individual Organelle Analysis: It allows researchers to study organelles individually, avoiding the complexity of the whole cell.

Study of Biochemical Pathways: It enables the investigation of biochemical pathways and interactions between different organelles.

Disease Research: It has been instrumental in understanding various diseases and developing new therapies.

Example of Cell Fractionation Application

Cell fractionation is frequently used to isolate mitochondria and study their role in cellular respiration. Researchers can use the isolated mitochondria to:

Measure oxygen consumption.

Analyze the activity of respiratory enzymes.

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