Simple diffusion: molecules are moving all the time due to random thermal motion
- Will move down concentration gradient due to their random thermal motion
- Will continue to do that until distribute equally
- At this point, no concentration gradient, reached chemical/dynamic equilibrium (will continue to
move down concentration gradient until reach chemical or dynamic equilibrium)
- No conc gradient, no NET movement (still bouncing around) but no NET movement of our
glucose molecules
- The driving force is always the concentration gradient whenever we talk about diffusion
Blood contains oxygen, glucose, these molecules can diffuse through slits/pores in capillary, the oxygen
will diffuse out of the capillary and diffuse down its concentration gradient (partial pressure gradient)
and diffuse towards cells
High conc of glucose in capillary, it will diffuse out and move towards the cells (simple diffusion in the
body)
***SIMPLE DIFFUSION IS NOT VERY EFFICIENT OVER LONG DISTANCES
Calculate time for diffusion : x is the distance the molecule is travelling divided by the diffusion
coefficient
Time for diffusion will increase with the square of the distance
The further the molecule has to diffuse, takes much much longer
Generally most cells in the body are very close to blood vessels (in general)
Can the human body change the diffusion distsance? If so how? – grow more cells in certain areas
(maybe not), dilate the blood vessels, create more vessels,
Exercise can cause angiogenesis (development of new blood vessels) – more blood vessels through
tissue bed means more cells closer
Diffusion through cell membrane (how are they going to get into the cell)
- Those substances must be non polar (lipid soluble) in order to penetrate the lipid (fatty acid tail)
region of the lipid bilayer
- Fatty acid tail barrier: substances have to be lipid soluble (non polar molecules)
- The driving force is still the concentration gradient
- Molecule, under random thermal motion, will diffuse through cell memembrane until reach
electrochemical equilibrium
- Rate of diffusion can be predicted by Fick’s First Law of Diffusion
Polar molecules cannot diffuse directly through the cell membrane due to the hydrophobic fatty acid
region: - require protein chanel/pore (leak channel) – holes lined with proteins, driving force is sitill
concentration gradient
Na+ has large watershell, so acting like a larger molecule (potassium’s will be much smaller water shell)
- if sodium came to potassium channel, cannot strip off the water shell
- water shell must be removed byt hes pecific channel (na+ channel can only strip off water shell
of na+)
Some of these factors acta s ‘filters’ preventing one ion from passing through another ion’s channel –
this is NOT chemical specificity (that requires binding directly to protein)
- the ions moving through the protein channel does not require the ion to bind directly to the
protein
- so NOT chemical specificity
membrane permeability:
- chloride is most permeable, Na+ is least permeable; not permeable to sodium, quite permeable
to potassium, more permeable to chloride
Facilitated diffusion; large molecules greater than 0.8 nm – binding to an intergral membrane protein ---
***BINDING*** causing the proteins to change shape, conformational change in that protein moving
the molecule across the membrane – when the protein changes shape, it shuttles the molecule across
the membrane – this is still powered by the concentration gradient, but called a carrier mediated
transport (protein is carrying the molecule across the membrane)
- chemical specificity
- can be competitively inhibited by molecules that are structurally similar to the one that should
be carried
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