![](https://images.ecency.com/DQmParFCHQLVXV4RwxjXjxRNMhrAGkFtMVQb995ukiJen3P/_1b767a50_7fab_4014_949d_854b0f7235a8_.png.jpg)
 
Hi, Scientist! Welcome to my blog.

Here, I’ve discussed the concept of receptor-mediated endocytosis. Additionally, you can check out the video for a detailed explanation of the process—though only Steps 1 to 4 are covered. I trust you’ll find it helpful!
[Click to watch video](https://ecency.com/stemsocial/@aristotle01/jgnwpwkkih)

Or 


<center>[![](https://ipfs-3speak.b-cdn.net/ipfs/bafybeid6ikyi6zy5pfmhi3iakfmqlfyfiatuz7nyzkty3g7nxwhll43lei)](https://3speak.tv/watch?v=aristotle01/jgnwpwkkih)</center>


**Steps:**

1.  Ligand Binds to the Receptor First things first! This is where it all kicks off. Specific molecules floating outside the cell, which we call ligands, find their perfect match – a receptor protein – on the cell's outer membrane, the plasma membrane. These receptors aren't just scattered randomly; they often hang out in special little dips in the membrane, which we cleverly call clathrin-coated pits. It's like they're waiting for their VIP guests, the ligands, to arrive! Receptor-ligand binding (e.g., LDL + LDL receptor) must occur before this pit gets formed
    
2.  Receptor-Ligand Moves to Clathrin-Coated Pit: So, once a ligand snuggles up to its receptor, they form a receptor-ligand complex. These complexes then start to gather and cluster together right there in those clathrin-coated pits. Now, here's where it gets cool: this binding triggers a signal that makes a specific phospholipid component, PIP2 (Phosphatidylinositol 4,5-bisphosphate), stick to an adaptor protein (AP2). And guess what? When AP2 binds to PIP2, it actually changes its shape – a conformational change – which is a super important step for what comes next!
    
3.  Membrane Folds Inwards: Now that AP2 is activated and binding, the clathrin protein (you can picture it as a blue dashed structure, like a cage in the making) on the inside of the membrane starts to assemble. This assembly literally pulls the membrane inwards, causing it to invaginate or fold, forming a deeper and deeper pit. As more and more of those receptor-ligand complexes pile into the pit, it just keeps getting deeper, forming a distinct flask-shaped indentation.
    
4.  Vesicle Enters: At this point, the neck of that flask-shaped invagination gets a visit from another important protein called dynamin. Dynamin acts like a molecular "string-puller" or "scissor," pinching off the neck of the invagination. Voila! This releases a brand new, fully formed clathrin-coated vesicle into the cell's cytoplasm. Inside this little bubble, you'll find all those internalized ligand-receptor complexes, plus a tiny bit of extracellular fluid.
    
5.  Loses Clathrin Coat (Uncoating): Once that clathrin-coated vesicle is safely inside the cell, it doesn't stay coated for long. The clathrin coat (those blue boxes you might imagine) quickly falls apart, or disassembles. This "uncoating" process needs energy, and it's crucial because the clathrin coat would actually prevent the vesicle from fusing with anything else. The disassembled clathrin bits are then recycled back to the plasma membrane, ready for their next job!Now, the newly uncoated vesicle is free! Its next stop is to fuse with an early endosome. Think of endosomes as the cell's sorting centers. They're membrane-bound compartments that act like a busy post office, directing where everything goes next.
    
7.  Receptor and Ligand Separates: Inside the endosome, things get sorted out. The environment inside the endosome is slightly acidic (thanks to little proton pumps working hard!), and this acidity often causes the ligand to detach from its receptor. This separation is key for the next steps! The endosome then gets to work, sorting all the internalized stuff.
    
8.  Ligands Go to Lysosomes or Golgi for Processing: Once separated, the ligands typically have a one-way ticket. If they're nutrients or signaling molecules that need to be broken down, they're usually sent to lysosomes (often via late endosomes). Lysosomes are like the cell's recycling and waste disposal centers, packed with powerful digestive enzymes that break down the ligands into their basic building blocks, which the cell can then reuse. Sometimes, ligands might even head to the Golgi for further processing, depending on their role.
    
9.  Receptors Move to the Membrane:  Meanwhile, many of the receptors have a different destiny: they're recycled! They bud off from the endosome in new vesicles and are transported back to the plasma membrane. This means the cell can reuse them over and over again to bring in more of the specific ligands it needs. Pretty efficient, right? In some special cases, both the ligand and receptor might be transported across the entire cell to another membrane (a process called transcytosis), or sometimes, even the receptors themselves are sent to the lysosomes for degradation if the cell needs to reduce its sensitivity to a particular signal.
    
9.  Vesicle Fuses with the Membrane: For the recycled receptors, their journey culminates when the vesicle carrying them fuses back with the plasma membrane. This replenishes the cell surface with receptors, ready to bind more ligands.
    
10. Exocytosis: During exocytosis, the contents released after a vesicle fuses with the plasma membrane depend on the cell type and vesicle function.


These steps areincredibly important for so many cellular functions – from grabbing essential nutrients like cholesterol to responding to hormones and even how some viruses manage to sneak into our cells! It's a truly remarkable and highly regulated process.

<a href="https://ecency.com/hive-158694/@aristotle01/science-arts" target="_blank">Click to know how I created this image</a>

#stemsocial#science

Thanks @stemsocial for this great opportunity to write on this platform. 

Thanks everyone.