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MCAT
Course: MCAT > Unit 6
Lesson 2: Transport across a cell membrane- Transport across a cell membrane questions
- Passive transport and active transport across a cell membrane article
- How do things move across a cell membrane?
- Passive Transport by Facilitated Diffusion
- Diffusion and osmosis
- Exocytosis
- Phagocytosis
- Membrane potentials - part 1
- Membrane potentials - part 2
- Permeability and membrane potentials
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Passive Transport by Facilitated Diffusion
Created by Raja Narayan.
Want to join the conversation?
- Why doesn't this conformational change use energy?(5 votes)
- I am not 100% sure if this is correct but from my experience I think that when the ion binds to the protein, the protein takes on a "high-energy" state. I think that the protein will undergo this shape conformation in order to move itself into a new and more comfortable "low-energy" state. Again I could be totally wrong on this.(6 votes)
- Hi guys. As mentioned in the previous chapters, there are two types of integral protein - carrier and channel protein.
So my qns is: Does facilitated diffusion involve a carrier protein or channel protein ? This video used only carrier protein as an example.
Thank you :)(5 votes)- Carrier proteins are used, no channel proteins (for passive diffusion) or ATP is needed.(5 votes)
- is facilitated diffusion only used for chloride?(4 votes)
- No, facilitated diffusion just describes any transportation that requires proteins to help molecules cross the membrane down its gradient (does not require ATP or energy)(3 votes)
- Atwhen the Cl- ion faces inside of the cell membrane, is that done by flippase? Or is this part of "confirmational change?" Thank you. 3:10(2 votes)
- I think flippase requires ATP, and this does not. I think this conformational change happens due to the concentration gradient, rather than via a catalyst.(2 votes)
- Just wandering... This protein are made of A.A. ok.. Some A.A. are polar that this include the acid and basic, and other non-polar. Thats ok.. but the question arise when the tutor say that the protein is in the uncomfortable shape when is bind to de Cl. That stress that give the Cl ion is because the A.A. that make the inside of the channel that can pass this Cl are non-polar? and just also wandering the A.A. that are in the out side face of the protein that are making the interaction with the hydrophobic part of the phospholipid are non-polar?? And what about the A.A. on both tips of the protein that are making interaction with both the polar part of the phospholipid and the non-polar part of this phospholipid.... Just thinking if anyone can help clarified myself thanks(2 votes)
- Binding of the Cl- ion makes a conformation change in the protein. You have to think about the Induced fit theory for enzymes. When an enzyme binds its ligand, both the enzyme and the ligand change their shapes slightly to enable the binding. The stress is due to the change in conformation of the active site, which can effect the rest of the enzyme shape.
The area of the protein that is contact with the phospholipid membrane is comprised of hydrophobic parts, where the areas of the protein which are in contact with the intra/extracellular environments are hydrophilic. So anything embedded in the plasma membrane is hydrophobic.(1 vote)
- What's the difference between Facilitated Diffusion via this transmembrane integral channel protein in the video, and ligand-dated ion channels? Both would let the Cl- ion through, right?(2 votes)
- I could be wrong and please correct me if I am, but from my understanding, ligand-gated ion channels remain open for as long as the ligand is bound. But carrier proteins, like the one mentioned in the video, carries one ion at a time.(1 vote)
- Another example of facilitated diffusion is via channel proteins. Is all transport via channel proteins considered facilitated diffusion (thus passive transport)? Example: Un-gated channels would be passive and thus be facilitated diffusion. But what about voltage gated and ligand gated channels?(1 vote)
- Facilitated diffusion really only relies on 2 things:
1) The chemical in question is moving down its gradient. This may be an electrochemical gradient.
2) The chemical in question is able to move due to some protein "clearing the way" for the chemical to move.(3 votes)
- What is the exact term for the protein changing shape or "flipping" as Raja mentioned in the video,? 3:20(1 vote)
- Changing conformation is the "real" term. As noted by the Khan Academy staff, the protein never actually flips 180 degrees; it just changes conformation that looks like the flipped form.(2 votes)
- Doesn't the carrier protein require ATP to change conformation? i thought this process was active transport, and facilitated diffusion is when molecules move into or out of the cell via trans-membrane protein channels.(0 votes)
- No, ATP isn't required to make the protein change shape in this example. Both protein channels and this type of transport protein are moving ions/molecules down their gradients, so they don't require energy. Active transport moves a solute against its gradient, therefore requiring energy. An example of active transport is the sodium-potassium pump.(3 votes)
- My question is somewhat general. I am wondering about these proteins. Do they "immerge" when a chemical is near or are they always in a certain position? In my mind, I am picturing a cell with millions of different proteins that are lined up in such a way that that each occupy their own position along the cell. I want to make sure this is right? How many different binding sights are there?(1 vote)
- Yes your mental image seems to be correct — for most cell membranes the entire surface of is studded with various proteins including transporters and channels. I've seen estimates of up to a million copies of a single membrane protein per cell! Another source claims ~30,000 intergral membrane proteins per square µm.
This§ free online textbook claims that from 25-75% (by mass) of a cell membrane will be protein.
Does that help?
§Ref: https://www.ncbi.nlm.nih.gov/books/NBK26878/(1 vote)
Video transcript
- [Voiceover] Alright, so in this video we're going to talk
about passive transport. So let's start off
taking a look at a cell. So there's the cell right there, and why don't we just zoom in up here. And let's focus in on the membrane. And as you know it's a lipid bilayer which basically means that we have these hydrophilic heads
that are sitting over here. So I'll draw just a few of them,
so three of them right here and then three of them right here as well. And they've got hydrophobic tails. These are fatty acid tails
that come down like this. So they are kinked like that, and that's what makes the hydrophobic core of our lipid bilayer. And I could go on and
draw this all the way but I'm just going to
have this blue outline as our hydrophilic head, down
here as well, hydrophilic head and the hydrophobic tail
is inside, this gray area. And so the question arises then, when we have a small particle, let's say this is a chloride ion, Cl negative, that's sitting right there, how do we get it from the outside area, the extracellular space, so I'll say out, this is from the outside, to the inside right here. And in our gut, which
is where this example is going to take place, we
do that by passive transport, and as we talked about earlier, there are four different
types of active transport, and the main type we're going
to focus on in this video is what's called Facilitated Diffusion. Facilitated Diffusion,
because we're diffusing or we're moving across a certain space. But the question here is, what's
facilitating that movement? And therein lies the answer of what we're going to
focus on for this video. So along our cell membrane there are also going to be proteins that are embedded along the cell membrane, And so what's going to
facilitate the movement of this chloride ion across
from the outside to the inside is this chloride channel right here. And so this channel is
built in a funny way that has this little pocket
that sits right there and it's shaped like that. And the idea behind this pocket is that it's the site where chloride, and specifically chloride, can sit down. So if I were to go through
and draw it sitting in here it would look a little bit like this. Not too different from what I just drew, but there's a very important distinction that we're going to have to make here. Now, what happens is that now that our chloride is sitting here, we've made this chloride channel
right here uncomfortable. Now we're uncomfortable, it doesn't want to sit like
this now because now that we're holding the chloride ion we
want to change our posture. And so what happens is
that our chloride ion will actually snap and change its shape. And it'll snap in such
a way that it'll flip. And when it flips like
this, which you'll notice is at the part that was
holding on to our chloride, the part that was holding
on to our chloride will now suddenly be facing
the intracellular face of our cell membrane,
which sure enough means that the chloride ion can now leave. Leaving behind then the same protein that we started off with right here. But now it's a little different. Now, as you can see,
it's got the same shape, but instead it's clearly
missing our chloride ion. And so what's happened along the way is that when we made the switch here from this uncomfortable shape to this relatively more comfortable shape it allowed our chloride to exit. And now that it's exited
into the inside of our cell, our protein has become
uncomfortable again. And so now that it's
uncomfortable it needs to shift. And when it shifts, what shape do you think it's going to take? I think you probably guessed it. It's going to look exactly
like what the protein did before it made contact with the
chloride in the first place. And so now it's comfortable again, so it's nice and comfy. And in fact it's ready to
take on another chloride ion. And so what our protein
is doing along the way is that it's changing... it's changing its conformation,
and the conformation is just the pose the protein is taking. And it changes its conformation, whether it's binding the chloride ion, as it did here to become more comfortable, or if it's not holding the chloride ion, as it did here when it was uncomfortable, to shift always to a more
comfortable position. And through this process,
in a very step-wise way our chloride ion is able to enter the cell without using any energy whatsoever. No ATP is used at all,
instead this protein is used to facilitate the movement of
the chloride into the cell.