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AP®︎/College Biology
Course: AP®︎/College Biology > Unit 2
Lesson 1: Cell structures and their functionsEndoplasmic reticulum and Golgi bodies
During protein synthesis, proteins meant for use within the cell are translated by free ribosomes. Proteins meant to be embedded in the cell membrane or used outside the cell are translated by ribosomes attached to the rough endoplasmic reticulum. These proteins are then transported to the Golgi body for further maturation and sorting before being released. Created by Sal Khan.
Want to join the conversation?
- Just a quick question. What dictates whether or not a strand of mRNA attaches to a free-floating ribosome as opposed to one attached to the Rough E.R.? Or is it just a "luck of the draw" sort of thing?(163 votes)
- In eukaryotes, free ribosome's actually assemble around the mRNA then will begin reading the code. Fairly early on a certain sequence in the RNA may be recognised which causes the whole translation process to halt while the mRNA-ribosome complex is all transferred to the endoplasmic reticulum, translation will then begin again with the growing polypeptide chain entering the ER lumen. The process is known as cotranslational localisation. Generally speaking, proteins that are destined for lysosomes, membranes or to be secreted from the cell are made on the RER.(138 votes)
- does each cell have only one E.R, and Golgi body?(55 votes)
- As I am sure you know, the ER (endoplasmic reticulum) is a network of cisternae around the nucleus. Thus, there is only one network of ER in a cell, but within that is a number of sacs and tubes that make up the entire ER. As for the Golgi apparatus (or body), is to is made up of multiple sections of cisternae (just like the ER, yet in a different formation), and there are often multiple complexes of Golgi to be found in a single cell, with the maximum being ~20.(66 votes)
- If the proteins take part of the membrane of the ER when they turn into vesicles, how does the ER reattach? Does the ER become smaller and smaller every time? Does it grow to keep up with how much of its membrane is lost?(44 votes)
- At the same time that vesicles pinch off of the ER, there are vesicles arriving at the ER, restoring its share of membrane. The net result is that it doesn't really change in size.(45 votes)
- atwhat is chromatin? 2:03(18 votes)
- Chromatin is a combination of DNA and protein, and is what makes a Chromosome. It has many functions, but mainly a way to efficiently pack in as much DNA as possible, and improve the strength of the structure.
DNA strand wraps around protein histones, to form a nucleosome, it looks like 'beads on a string'. This in turn wraps around on itself to create a '30 nm structure', and wraps around on itself again.
If you google image 'Chromatin' you will see what I mean, there are some good diagrams illustrating it.(34 votes)
- Does the vesicle have two membranes around after it has ripped through the membrane of the E.R. and the Golgi body ?(19 votes)
- No. When a vesicle comes in contact with a membrane in the ER or Golgi body, the membrane does not wrap around it to create another membrane. Instead, the two membrane's fuse, so the contents are released into the lumen of the ER or Golgi body (as at). Then, when the contents leave again, a new vesicle will form around them. 10:32(22 votes)
- I have heard that the smooth ER gets rid of toxins. What toxins are these exactly and how would they get in the cell at all?(16 votes)
- One example of a toxin is alcohol. Liver cells of alcohol drinkers have a lot of smooth ER because it helps to detoxify the alcohol. If the smooth ER were absent or dysfunctional, the cells would shrivel up and die. This can lead to cirrhosis. SER also protects cells from harsh effects of drugs. There are also toxins produced by cellular processes that the SER take care of. Diffusion, Facilitated diffusion, active transport, and endocytosis are some ways that toxins enter the cell.(20 votes)
- What is the E.R lumen and what purpose does it serve?(12 votes)
- The word lumen is used a lot in biology for the space inside a tube, such as the inside of blood vessels or intestines. It is also used for the space inside the E.R(22 votes)
- Okay, so I get the basic idea but, exactly what is the difference between transcription and translation.(11 votes)
- Transcription makes messenger RNA from DNA. Translation makes proteins from messenger RNA.(13 votes)
- Why is it that a protein has to go through the Golgi Body after exiting the ER, Sal mentions that it goes through a maturation process, but what does that actually do? Why can't the vesicle made from the ER transport its protein straight to its final destination?(8 votes)
- Great qustion!
You canthink of the Golgi bodies as the post office of the cell. Before anything goes out, the golgi body sort of packages it with materials which will be easily given access to move through the cell membrane. This process is called glycolysation. If there were no golgi, then the protein may not have been given access to go through the plasma membrane due to the phospholipids. The vesicle made by the ER is designed to only go about the cytoplasm, not the plasma membrane.
Hope I helped.(5 votes)
- probably a silly question but: how fast is this process taking place?(6 votes)
- This is actually an excellent question! Generally speaking, protein synthesis occurs pretty quickly. The rate depends on the type of cell. For example: prokaryotes synthesize faster than eukaryotes. To give you an idea of how fast this is happening, some prokaryotic cells are known to synthesize proteins at a rate of 20 amino acids per second.
Now in this video there are other processes going on besides just synthesis like transportation. But since these processes involve newly manufactured proteins you can imagine that they take place at relatively fast rate as well.(4 votes)
Video transcript
We've already talked
about the process from going from DNA
to messenger RNA. And we call that
process transcription. And this occurs in the nucleus. And then that messenger
RNA makes its way outside of the nucleus, and it
attaches to a ribosome. And then it is translated
into a protein. And so you could say that
this part right over here, this is being facilitated
by a ribosome. Or it's happening at a ribosome. With that high-level
overview, I now want to think a little bit
in more detail about how this actually happens, or the
structure of things where this happens inside of a cell. And so I'm going to now draw
the nucleus in a little bit more detail so that we
can really see what's happening on its membrane. So this right over
here is the nucleus. Actually, let me
draw it like this. And instead of just drawing the
nucleus with one single line, I'm going to draw
it with two lines. Because it's actually a
double bilipid membrane. So this is one bilipid
layer right over here. And then this is another
one right over here. And I'm obviously not
drawing it to scale. I'm drawing it so you can
get a sense of things. So each of these lines
that I'm drawing, if I were to zoom in on this--
so if I were to zoom in on each of these lines,
so let's zoom in. And if I got a box like that,
you would see a bilipid layer. So a bilipid layer
looks like this. You have the circle
is a hydrophilic end and those lines are the
fatty hydrophobic ends. So that's our bilipid layer. So that's each of these lines
that I have drawn, each of them are a bilipid layer. So the question is, well,
how does the mRNA-- obviously you have all this
transcription going on. You have the DNA,
you have the mRNA. It's all in here,
this big jumble of chromatin inside the nucleus. How does it make its way outside
of this double bilipid layer? And the way it makes its way
out is through nuclear pores. So a nuclear pore is
essentially a tunnel. And there are
thousands of these. It's a tunnel through
this bilipid layer. So the tunnel is made up
of a bunch of proteins. So this right over
here-- and this is kind of a cross
section of it. But you could almost
imagine it if you're thinking of it in
three dimensions, you would imagine a tunnel. A protein-constructed--
a tunnel made out of proteins that goes through
this double bilipid membrane. And so the mRNA can make its way
out and get to a free ribosome, and then be translated
into a protein. But this right over here is
not the complete picture. Because when you translate a
protein using a free ribosome, this is for proteins that
are used inside the cell. So let me draw the entire
cell right over here. This is the cell. This right over here is
the cytosol of the cell. And you might be
sometimes confused with the term cytosol
and cytoplasm. Cytosol is all the fluid
between the organelles. Cytoplasm is everything
that's inside the cell. So it's the cytosol
and the organelles and the stuff inside the
organelles is the cytoplasm. So cytoplasm is everything
inside of the cell. Cytosol is just the fluid
that's between the organelles. So anyway, the free ribosome
over here, this translation is good for proteins used
within the cell itself. The proteins can then
float around the cytosol and used in whichever
way is appropriate. But how do you get protein
outside of the cell, or even inside the
cellular membrane? Not within it, within
the cell, but embedded in the cell membrane or
outside of the cell itself. And we know that
cells communicate in all sorts of different
ways and they produce proteins for other cells or for
use in the bloodstream, or whatever it might be. And that's what we're going
to focus on in this video. So contiguous with this
what's called a perinuclear space right over here, so
the space between these two membranes-- So you have
this perinuclear space between the inner and
outer nuclear membrane. Let me just label that. That's the inner
nuclear membrane. That's the outer
nuclear membrane. You could continue this
outer nuclear membrane, and you get into these kind
of flaps and folds and bulges. And this right over
here is considered a separate organelle. So you get this thing
that looks like this, and I'll just do it the
best that I can draw it. And this right
over here is called the endoplasmic reticulum. So this right here is
endoplasmic reticulum, which I've always thought would
be a good name for a band. And the endoplasmic
reticulum is key for starting to produce and then later
on package proteins that are either embedded in
the cellular membrane or used outside of
the cell itself. So how does that happen? Well, the endoplasmic reticulum
really has two regions. It has the rough
endoplasmic reticulum. And the rough
endoplasmic reticulum has a bunch of ribosomes. So that's a free
ribosome right over here. This is an attached ribosome. These are ribosomes
that are attached to the membrane of the
endoplasmic reticulum. So this region where
you have attached ribosomes right
over here, that is the rough endoplasmic reticulum. I'll call it the
rough ER for short. Perhaps an even better
name for a band. And then there's
another region, which is the smooth
endoplasmic reticulum. And the role that this
plays in protein synthesis, or at least getting proteins
ready for the outside of the cell, is you can
have messenger RNA-- let me do that in that
lighter green color-- you can have
messenger RNA find one of these ribosomes associated
with the rough endoplasmic reticulum. And as the protein
is translated, it won't be translated
inside the cytosol. It'll be translated
on the other side of the rough
endoplasmic reticulum. Or you could say on
the inside of it, in the lumen of the rough
endoplasmic reticulum. Let me make that
a little bit-- let me draw that a
little bit better. So let's say that this right
over here, that right over here is the membrane of the
endoplasmic reticulum. And then as a
protein, or as a mRNA is being translated
into protein, the ribosome can attach. And let's say that
this right over here is the mRNA that is
being translated. Let's say it's going in that
direction right over here. Here is the membrane of the ER. So ER membrane. This right over here-- and
actually, the way I've drawn it right over here, this is
just one bilipid layer. So let me just
draw it like this. I could do it like this. And this is actually, this
bilipid layer is continuous. It's continuous with the
outer nuclear membrane. So let me just make it like
that so you get the picture. And then at some point in
the translation process, the protein can be
spit out on the inside. As it's being translated,
it can be spit out on the inside of the
endoplasmic reticulum. So this is the lumen. This is the ER lumen
right over here. So we're inside the
endoplasmic reticulum here. Here we're outside
in the cytosol. So that way you get the
protein now, inside the ER. Inside the
endoplasmic reticulum, and it can travel through it. And at some point,
it can bud off. So let's say, imagine the
protein is right over here. And the smooth endoplasmic
reticulum has many functions, and I won't get into all the
depth of how it's involved. But at some point that
protein can bud off. So let me draw a
budding off protein. So let's say this
is the membrane of the endoplasmic reticulum. And a protein, let's say,
ends up right over here. And then it can bud out. So it could go from that to--
let me do that same color. It could go from
that to that-- I think you see where this is
going-- to that, and then to that. And then it could go
to something like this. Now it has budded out. And when you have a
protein, or really you have anything that's
being transported around a cell with its
own little mini membrane, we call this a vesicle. So now it'll bundle up,
and now it is a vesicle. Now, this vesicle
can then-- let me draw some of these vesicles
holding some proteins, so let me draw that-- can then go
to the Golgi apparatus, which I'll drawn in blue right
over here as best as I can. So the Golgi apparatus. This is not--
obviously there could be better drawings of
something like this. And then they can essentially
do the reverse process, and they can attach themselves
to the Golgi, oftentimes the Golgi body, named after
Mr. Golgi who discovered this. And then the proteins,
once they get into the inside
of the Golgi body, then they essentially go
into a maturation process so that they're ready for
transport outside of the cell, or maybe to be embedded
into the cellular membrane. So this right over
here is the Golgi body, or a Golgi body or
Golgi apparatus. And then once they're
done with that process, then this is kind of the
fully-manufactured protein ready to be used. And actually, maybe I'll make
it a slightly different-- well, I'll just use that same color. This is the
fully-manufactured protein. And now it can transport
to the cell membrane. And that protein can
either be transported outside of the
cell, or it can be embedded within the
membrane itself.