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STRUCTURE
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Phospholipd
bilayer
◦ Hydrophilic heads –
attracetd to water
◦ may face
aqueous solutions
– cytoplasmatic
and extracellular
fluids
◦ Hydrophobic tails –
repelled by water
◦ tend to avoid
water
◦ group together
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Fluid mosaic
structure
◦ The bilayer is held together
by weak hydrophobic
interactions between the
tails
◦ Hydrophilic / hydrophobic
layers control the passage of
substances
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◦ Individual phospholipids can
move within the bilayer,
allowing for membrane
fluidity and flexibility
PM is represented according to a fluid-mosaic model, as it is:
◦ This fluidity allows for the
spontaneous breaking and
reforming of membranes Fluid – the phospholipid bilayer is viscous and individual
phospholipids can move position
Mosaic – the phospholipid bilayer is embedded with proteins,
resulting in a mosaic of components
Phospholipids Proteins Cholesterol
PM components
glycoproteins
peripheral proteins
Proteins in • receptors
• immobilized enzymes
PM • adhesive proteins
integral proteins
• protein channels
• protein pumps
• receptors
◦ Jet Rat
◦ Junctions – Serve to connect and join two cells together
◦ Enzymes – Fixing to membranes localises metabolic
pathways
◦ Transport – Responsible for facilitated diffusion and active
transport
Membrane ◦ Recognition – May function as markers for cellular
identification
proteins’ ◦ Anchorage – Attachment points for cytoskeleton and
extracellular matrix
functions ◦ Transduction – Function as receptors for peptide hormone
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cholesterol
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Drawing the PM fluid mosaic model
◦ phospholipids
◦ double layer
◦ with heads and tails
◦ cholesterol
◦ small elements
between
phospholipids
◦ glycoproteins
◦ shown with sugar
chain on the external
end
◦ Transmembranous
◦ peripheral proteins
◦ at the surface
◦ integral proteins
◦ going through both
phospholipid layers
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In 1920s it was first proposed by Gortel and
Grendel that membrane contained a bilayer
of phospholipids
◦ It explains
impermeability of
membranes for many
substances
◦ Membrane visible as two dark lines with lighter band
Electron between them – proteins appear darker TEM mcrograms
microscopy than lipids, which seemed to fit Davson-Danielli’s theory at
the time
evidence
◦ However today we know, that on the photo there are two
bilayer membranes of two adjacent cells
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◦ Biochemical:
◦ Membrane proteins were discovered
to be insoluble in water (indicating Evidence
hydrophobic surfaces) and varied in against
size
◦ Such proteins would not be able to
Davson-Daniel
form a uniform and continuous layer li’s model
around the outer surface of a
membrane
Evidence against
Davson-Danielli’s model
◦ Electron microscopy:
◦ Freeze-fracture technique:
- Cells are rapidly frozen
- Then they are fractured
- Fractures occur along the weak lines within the cel
- It showed fractures between two lipid layers and
visualized globular protein structures localizing
them both around and across the membranes
The outline of the method. After ‘quick-freezing’ of cells, the cytoplasm is exposed by
‘fracturing’ of frozen cells with cooled knife. The ‘etching’ procedure induces
sublimation of water in the cytosol and the organelle lumen. This makes lipid droplets
stand out because lipid esters in the lipid droplet core do not sublimate. Vacuum
evaporation of platinum and carbon onto the surface makes a ‘replica’ of the cellular
ultrastructure.
https://bio-protocol.org/e2556
Evidence
against
Davson-Danielli’
s model
◦ Fluorescent antibody tagging
of membrane proteins
◦ Antibodies with fluorescent
labels were used to stain
membrane proteins
◦ Proteins of some cells were
tagged red, of other – green
◦ Cells were fused
◦ After some time it was visible
that red and green tags
became mixed
www.uaz.edu.mx
◦ It shows that position of
membrane proteins is not
fixed and form a static layer
Singer-Nichol
son – model
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TEXTBOOK CHAPTER 1.3 PAGES 25-33