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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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How do things move across a cell membrane?
Created by Raja Narayan.
Want to join the conversation?
- Im not smart enough to be here(1 vote)
- If you are here, you are smart enough to be here — if you are confused then it may be helpful to review some of the earlier material, for example the high school biology material could be helpful ...
Also, please remember that intelligence is not fixed. As you practice using your mind you get smarter – e.g. by working hard on problems and learning from your mistakes. So, the more time and effort you spend here, the smarter you will get!
You might find this article interesting:
https://blogs.scientificamerican.com/guest-blog/you-can-increase-your-intelligence-5-ways-to-maximize-your-cognitive-potential/
Take care and don't beat up on yourself - that definitely does not help.(22 votes)
- Is endocytosis and phagocytosis the same thing? if not, what is the difference between the two?(5 votes)
- Phagocytosis is a specific type of endocytosis. Another example of endocytosis would be macropinocytosis where cells engulf fluid.(10 votes)
- For endocytosis, how is the vesicle created extracellularly? I thought the process was:
(1) some extracellular substance, say a protein, binds with a receptor on the cell's membrane
(2) the cell membrane invaginates and "reaches" around the protein, enveloping it
(3) the cell membrane, having surrounded the protein, pinches off, creating an intracellular vesicle containing the protein.
Does my description only describe phagocytosis, or most/all endocytosis?
Thanks!(6 votes) - What is gradient?(0 votes)
- A gradient just means a difference between two different sites. Think of this:
Side A: [:::::..:.:.:.:.:.......... . . . . . . . . . . . ] Side B
There is a gradient in dots between side A and side B. At side A there is a large concentration of dots. At side B there is a small concentration of dots.(8 votes)
- Atit says , "When there's an open channel or an open gate present, potassium naturally wants to flow down, its concentration gradient to go outside of the cell." Is an open channel or gate present at all times? If not when is is open? 2:15(2 votes)
- It's a leak because its always open, it is not like an ion-gated channel that needs to react to the activation of a ligand, the potassium leaks out to balance the concentration outside of the cell as well and keep the concentration gradient flowing(1 vote)
- Why is it that the secondary active transport is considered to be using energy in the form of establishing a gradient, but the K+ leak channel isn't considered to be using energy even though it also relies on establishing a gradient beforehand?(1 vote)
- Because in secondary active transport, you are using the energy of a gradient, like of H+ for example, to move something else to a place it doesn't want to go (against its own gradient). This original H+ gradient had to be set up using energy by the cell, so in a secondary manner energy was expended by the cell to move another molecule.
A K+ leak channel is just like an open pore in the cell that let's K+ go through down its gradient. It isn't using this to push anything else against its gradient, so it's not using any of the energy release by letting K+ go down its gradient for transport. While it's true that the K+ gradient took energy to set up, in this case the gradient serves a different purpose than for transport.(3 votes)
- Is there any organelles involved? If so, what are they and what is their part?(2 votes)
- Is endocytosis and phagocytosis the same thing?(1 vote)
- No, phagocytosis is a type of endocytosis. Phagocytosis differs from other methods of endocytosis because it is very specific and depends on the cell being able to bind to the item it wants to engulf by way of cell surface receptors.(1 vote)
- The video creator's repeated flaw of not naming a topic until AFTER he has gone through the whole explanation of that topic makes this video very hard to comprehend, learn from, and take notes off of.(1 vote)
- How does the protein vesicle referenced atform in the first place? Does it always come from another cell? 9:30(1 vote)
Video transcript
- [Voiceover] In our bodies, the cell is the smallest unit of life,
and just like larger units of life, like the entire human body, the cell needs nutrients that are, at times, available outside
of their cell membrane, and they also make waste
products that they need to get outside in order to survive, and so an important function of living is the ability to transport things, to transport things
across a cell membrane, to transport things
across a cell membrane. In the next couple of
videos, we're going to talk about these different types
of transport mechanisms. In this video, in particular,
I'll give you an overview of the different types
before we go into detail. A good rule of thumb to have
in the back of your head as we talk about this is
that the bigger the passenger or the bigger the waste
product or the nutrient that we're going to be
talking about that we need to transport across our cell membrane, that means the bigger the car that we're going to need to get them across. You'll see that as we
go in order right here from the smallest solutes or nutrients or waste products to the largest things that we transport across
our cell membrane. We've got specialized mechanisms
to make these things move. The first example of a transport mechanism I want to talk about is just a simple potassium leak channel. I'll call this a potassium leak channel, and you might be wondering, "Well, why do we call it a leak channel? "Why don't we just call it
just a regular channel?" Well, the reason is that potassium has a large concentration
inside of our cells. In fact, there are more potassium ions that are found inside of our cells than there are outside of our cells, and this is the exact opposite of what we see compared to sodium. For sodium, there's a ton of sodium ions that hang out outside of the cell, so they have a large concentration here, and there's a smaller portion of them that are located inside of the cell. When there's an open channel
or an open gate present, potassium naturally wants to flow down its concentration gradient
to go outside of the cell. This type of transport mechanism is called passive transport,
passive transport, and we'll talk about another
mechanism in a moment that's called active transport. Why do we call this passive? Well, the reason we make this distinction is because no energy was used in order to allow our potassium ion to
transport across the membrane. Now, at this point, I also want to mention that there are a couple
of different flavors of passive transport we'll
talk more detail about. There's something that's called diffusion, which is the movement of solutes in space, and we'll talk about
that, what that means. There's osmosis that relates mainly to the movement of water, and
then there's also filtration. We'll talk about filtration
as it occurs in the kidney, and then finally, there's also what's called facilitated diffusion, facilitated diffusion,
which, unlike diffusion as I've listed above,
facilitated diffusion utilizes the help of a protein channel, which is exactly what we
talked about right here. This is facilitated diffusion
that I gave you the example of for the potassium leak channel. Now, the other thing you
should be asking yourself is, "How is it that we had
a large concentration "of potassium in the
cell in the first place "or a large concentration of
sodium outside of the cell?" Well, the honest answer
is that there was energy that was used to set up that ion gradient, and so here we go. We're going to move towards
a bigger concept here where instead of just
moving one ion across, we're going to move two at the same time, and truth be told, it's a little
more complicated than that, but just to simplify it for now, we're going to talk about a process that allows for sodium to be pushed against its concentration gradient to be kicked out of a cell to
a place where there's already a bunch of them hanging
out, as well as potassium, moving from a place where it's
very comfortable and happy into this area where there is already a high concentration of potassium ions. This is not the direction
these ions wants to flow. In fact, we're going to need a little bit of energy to make that
happen, and so that energy is in the form of ATP, so
that's adenosine triphosphate, which is broken into adenosine
di--, as in two, phosphate, and there's a little phosphate group that broke off here as well. This protein is affectionately called a sodium potassium pump, a sodium potassium pump, and in some books, you'll see it called a sodium potassium ATPase because you break them all,
you'll have ATP to use it. This is an excellent example of something that's called active
transport, active transport, and as the name suggests,
relative to when we talked earlier about passive transport,
active transport uses energy, and it uses energy in this scenario by breaking a molecule of ATP. Now, as sort of a side note here, this is specifically known
as primary active transport because we've directly used ATP here. A direct use of ATP is
primary active transport, which may lead you to ask,
"Well, are there other types "of active transport as well?" The answer to that question is yes, you are absolutely
correct, and I'll give you an example from the gut. In the gut, when we eat things like salty food might
have some sodium in it, or it might be sweet food
and it's got some glucose in it as well, and as you already know, there's a lot of sodium that's outside of our cells, in the extracellular space. Well, our intestines, our guts, are lined with things that
are called enterocytes, and they're just basically
cells of the G.I. tract, and they're just like normal cells where they want sodium to enter. This protein that's on our enterocyte here will let sodium enter, but
because we're in the gut, another magical thing happens. This glucose molecule will enter as well. This is an example of something
that's called symport, symport, where both molecules are moving in the same direction,
one where we're using sodium to flow down its ion gradient and then glucose, going from outside of the cell into the cell. It's basically coming along for the ride, which is why this is a great example of what's called secondary
active transport, secondary, meaning that we used energy. Certainly we use energy here, so I'll say it uses energy here but not directly. This, in fact, uses a gradient
that was already set up, so a gradient set up using energy. In that sense, it's indirectly
using our ATP molecule, or indirectly using our energy that generated this sodium gradient. That's what happens when we have our sodium and our glucose
absorbed into our intestine. After it's absorbed into our enterocytes, they actually need to
go to our bloodstream, so I'll draw a little
blood vessel right here. That's where our nutrients need to go to to flow elsewhere in our body. In order to get out of our enterocyte and end up in our bloodstream, we actually use the same type of channel to help our glucose
molecule that just entered our enterocyte to leave the cell and travel to this blood
vessel or this capillary. What's unusual is that, again, sodium is in play here, but this time, it's actually going in
the opposite direction, but this completely makes sense. Remember, there's a higher
concentration of sodium outside of our cells, and so it naturally wants to flow down its ion
gradient into the cell. Still, this is an example of
secondary active transport, but instead of symport, now we have what's called antiport, antiport because our
two molecules are moving in the opposite direction of each other. We'll talk again about
secondary active transport in a part of the kidney call the nephron. For now, let's talk about bigger molecules trying to cross the membrane. As you see, we've been getting progressively larger from one ion to two ions to now we're talking about a bigger molecule like glucose. What about if we have a giant protein that wants to enter the cell? What I've drawn here is not the protein. Instead, I'll draw the
protein inside of here. I'll just write a.a. because you know proteins are made of amino acids. There's a couple of amino acids in here that want to enter our cell. This guy is a vesicle. A vesicle is just a small pocket of cell membrane that's
surrounding some type of cargo or some type of thing
we're trying to transport. In this case, it's this protein. Remember, it's the exact same membrane we have around our cell,
and once this vesicle gets close enough to
our membrane right here, it'll actually fuse, and in doing so, will then create an opening
from the inside of the vesicle, connecting it to the inside of our cell, which means that our amino
acid can actually enter inside. These steps that we saw
here as we went from here to allow our amino acid to enter the cell is a process that's called endocytosis, endocytosis, which as you can see here, means for something to
go into a site or a cell. Because we're moving something larger than what we talked about before, this uses a lot of energy,
uses a lot of energy directly here to make this process happen. You can actually have the
opposite case as well, where a vesicle that's
made inside the cell, as we'll talk about
sometimes will be made off of what's called the Golgi apparatus, and that's an organelle within your cell. It'll create a vesicle that'll have some protein that we want to get rid of. I want to make this different, so instead of amino acids in here, I'll write ACh or acetylcholine, which is a type of neurotransmitter
we have in our body. Once this vesicle with
acetylcholine is made from the Golgi apparatus, it floats towards our cell membrane,
similar to how we saw earlier, and then these membranes will fuse, the membrane of our vesicle,
as well as the membrane of our cell, causing the
acetylcholine to be kicked out. This process where this vesicle came here and then caused the acetylcholine
to get out of our cell is called exo, exocytosis, which is why I called it the opposite of endocytosis
because something is exiting our site or a cell, and this is similar to endocytosis in that it uses a lot of energy to happen. These are all the main
processes or mechanisms we use to move things
across our cell membrane, and they're very important to understand. Just to give you kind of an idea why, when things are wrong with our proteins or when viruses hijack some
of the mechanisms that we use to move things across our
membrane, bad things can happen. The more we know here,
the better we can fight a lot of our different
infectious diseases.