Skills: Membrane Structure & Transport (DP IB Biology: HL)

Membranes

• Membranes are vital structures found in all cells
• The cell surface membrane creates an enclosed space separating the internal cell environment from the external environment
• Intracellular membranes (internal membranes) form compartments within the cell, such as organelles (including the nucleus, mitochondria and RER) and vacuoles
• Membranes not only separate different areas but also control the exchange of materials passing through them; they are partially permeable
• Membranes form partially permeable barriers between the cell and its environment, between cytoplasm and organelles and also within organelles
• Substances can cross membranes by diffusion, facilitated diffusion, osmosis and active transport
• Membranes play a role in cell signaling by acting as an interface for communication between cells

Membranes formed from phospholipid bilayers help to compartmentalise different regions within the cell, as well as forming the cell surface membrane

Fluid Mosaic Model

• The fluid mosaic model of membranes was first outlined in 1972 by Singer and Nicolson and it explains how biological molecules are arranged to form cell membranes
• The fluid mosaic model also helps to explain:
  • Passive and active movement between cells and their surroundings
  • Cell-to-cell interactions
  • Cell signalling

• The fluid mosaic model describes cell membranes as ‘fluid’ because:
  • The phospholipids and proteins can move around via diffusion
  • The phospholipids mainly move sideways, within their own layers
  • The many different types of proteins interspersed throughout the bilayer move about within it (a bit like icebergs in the sea) although some may be fixed in position

The main components of cell membranes. The distribution of the proteins within the membrane gives a mosaic appearance and the structure of the proteins determines their position in the membrane.

• Analysis of evidence from electron microscopy led to the proposal of the Davson-Danielli model
• Other methods were then used to further investigate the model and suggested evidence against the model
  • Freeze-etchings
  • Fluorescent markers of membrane proteins

Transmission electron micrograph (TEM) of the plasma membrane

• When analysing transmission electron micrographs comment on:
  • How the membrane has two darker layers surrounding a lighter line
  • Proteins were known to appear darker in electron micrographs

TEM of a plasma membrane suggests evidence for Davson-Danielli's model

Freeze-etched electron micrographs

• When asked to analyse freeze-etched electron micrographs note that the very small bumps seen on the membranes are the integral proteins
• This provided evidence against Davson-Danielli’s model as it showed proteins extending into the centre of the membrane
• Be careful if the image is of a nuclear membrane as the larger circles represent the nuclear pores

Freeze-etching of a nucleus suggests evidence against Davson-Danielli's model

Fluorescent markers on membrane proteins

• When analysing data on the use of red and green fluorescent markers attached to membrane proteins, the key evidence to note, is that as time progresses after the fusion of the different cells with the different markers has occurred, more mixing of the markers is observed
• This evidence did not support Davson-Danielli’s model that the proteins were a uniform layer above and below the phospholipids
• It supported the ‘fluid’ part of Singer & Nicolson’s fluid mosaic model as it suggested that membrane proteins can move

Fluorescent markers on membrane proteins suggest evidence against Davson-Danielli's model

NOS: Falsification of theories with one theory being superseded by another; evidence falsified the Davson-Danielli model

• For about 30 years the technology available to scientists supported the Davson-Danielli model of membrane structure
• From the 1950's an advancement in technology led to the accumulation of evidence which resulted in the Davson-Danielli model being superseded by the Singer-Nicolson 'fluid mosaic model'

• Analysis of freeze-etched electron micrographs showed proteins extending into the centre of membranes
• Biochemical analysis of membranes suggested that it was unlikely proteins formed continuous layers because it showed:
  • Proteins were globular
  • Varied in sizes
  • They had parts that were hydrophobic
• The use of coloured fluorescent markers of antibodies showed that within forty minutes of fusing cells with different coloured fluorescent markers the markers had mixed
  • This suggested that membrane proteins were free to move within the layer