Alright. So now that we've covered molecular transport of really small molecules, including passive transport and active transport, we're finally going to move on to the last section of our map of the lesson on membrane transport. Now, the macro prefix and macromolecules really just mean large, and so macromolecules include really large proteins, polysaccharides, and DNA molecules as well. These macromolecules are simply just way too large to diffuse through membranes or channels, and so they will not be able to use the mechanisms of molecular transport that we talked about in our previous lesson videos, including the forms of passive transport or the forms of active transport that we discussed. Instead, these macromolecules must be transported across cell membranes using the process of either endocytosis or exocytosis, as you can see down below in our map. We'll be able to define endocytosis and exocytosis a little bit later in our course. But for now, I'd like to foreshadow for you guys that integral membrane proteins, very specific ones called fusion proteins, are really important to the process of endocytosis and exocytosis. These fusion proteins are integral membrane proteins that help fuse membranes, as their name implies, in both the process of endocytosis and exocytosis. Moving forward in our course, we're only going to talk about fusion proteins in the context of exocytosis, more specifically in the process of neurotransmitter release. However, it's important to keep in mind that fusion of membranes also takes place in endocytosis, and there are fusion proteins that we're not going to talk about that are involved in the process of endocytosis as well. Of course, because we're exploring our map using the leftmost branches first, in our next video we're going to explore endocytosis and the different types of endocytosis. So, I'll see you guys in that video.
- 1. Introduction to Biochemistry4h 34m
- What is Biochemistry?5m
- Characteristics of Life12m
- Abiogenesis13m
- Nucleic Acids16m
- Proteins12m
- Carbohydrates8m
- Lipids10m
- Taxonomy10m
- Cell Organelles12m
- Endosymbiotic Theory11m
- Central Dogma22m
- Functional Groups15m
- Chemical Bonds13m
- Organic Chemistry31m
- Entropy17m
- Second Law of Thermodynamics11m
- Equilibrium Constant10m
- Gibbs Free Energy37m
- 2. Water3h 23m
- 3. Amino Acids8h 10m
- Amino Acid Groups8m
- Amino Acid Three Letter Code13m
- Amino Acid One Letter Code37m
- Amino Acid Configuration20m
- Essential Amino Acids14m
- Nonpolar Amino Acids21m
- Aromatic Amino Acids14m
- Polar Amino Acids16m
- Charged Amino Acids40m
- How to Memorize Amino Acids1h 7m
- Zwitterion33m
- Non-Ionizable Vs. Ionizable R-Groups11m
- Isoelectric Point10m
- Isoelectric Point of Amino Acids with Ionizable R-Groups51m
- Titrations of Amino Acids with Non-Ionizable R-Groups44m
- Titrations of Amino Acids with Ionizable R-Groups38m
- Amino Acids and Henderson-Hasselbalch44m
- 4. Protein Structure10h 4m
- Peptide Bond18m
- Primary Structure of Protein31m
- Altering Primary Protein Structure15m
- Drawing a Peptide44m
- Determining Net Charge of a Peptide42m
- Isoelectric Point of a Peptide37m
- Approximating Protein Mass7m
- Peptide Group22m
- Ramachandran Plot26m
- Atypical Ramachandran Plots12m
- Alpha Helix15m
- Alpha Helix Pitch and Rise20m
- Alpha Helix Hydrogen Bonding24m
- Alpha Helix Disruption23m
- Beta Strand12m
- Beta Sheet12m
- Antiparallel and Parallel Beta Sheets39m
- Beta Turns26m
- Tertiary Structure of Protein16m
- Protein Motifs and Domains23m
- Denaturation14m
- Anfinsen Experiment20m
- Protein Folding34m
- Chaperone Proteins19m
- Prions4m
- Quaternary Structure15m
- Simple Vs. Conjugated Proteins10m
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- 5. Protein Techniques14h 5m
- Protein Purification7m
- Protein Extraction5m
- Differential Centrifugation15m
- Salting Out18m
- Dialysis9m
- Column Chromatography11m
- Ion-Exchange Chromatography35m
- Anion-Exchange Chromatography38m
- Size Exclusion Chromatography28m
- Affinity Chromatography16m
- Specific Activity16m
- HPLC29m
- Spectrophotometry51m
- Native Gel Electrophoresis23m
- SDS-PAGE34m
- SDS-PAGE Strategies16m
- Isoelectric Focusing17m
- 2D-Electrophoresis23m
- Diagonal Electrophoresis29m
- Mass Spectrometry12m
- Mass Spectrum47m
- Tandem Mass Spectrometry16m
- Peptide Mass Fingerprinting16m
- Overview of Direct Protein Sequencing30m
- Amino Acid Hydrolysis10m
- FDNB26m
- Chemical Cleavage of Bonds29m
- Peptidases1h 6m
- Edman Degradation30m
- Edman Degradation Sequenator and Sequencing Data Analysis4m
- Edman Degradation Reaction Efficiency20m
- Ordering Cleaved Fragments21m
- Strategy for Ordering Cleaved Fragments58m
- Indirect Protein Sequencing Via Geneomic Analyses24m
- 6. Enzymes and Enzyme Kinetics13h 38m
- Enzymes24m
- Enzyme-Substrate Complex17m
- Lock and Key Vs. Induced Fit Models23m
- Optimal Enzyme Conditions9m
- Activation Energy24m
- Types of Enzymes41m
- Cofactor15m
- Catalysis19m
- Electrostatic and Metal Ion Catalysis11m
- Covalent Catalysis18m
- Reaction Rate10m
- Enzyme Kinetics24m
- Rate Constants and Rate Law35m
- Reaction Orders52m
- Rate Constant Units11m
- Initial Velocity31m
- Vmax Enzyme27m
- Km Enzyme42m
- Steady-State Conditions25m
- Michaelis-Menten Assumptions18m
- Michaelis-Menten Equation52m
- Lineweaver-Burk Plot43m
- Michaelis-Menten vs. Lineweaver-Burk Plots20m
- Shifting Lineweaver-Burk Plots37m
- Calculating Vmax40m
- Calculating Km31m
- Kcat46m
- Specificity Constant1h 1m
- 7. Enzyme Inhibition and Regulation 8h 42m
- Enzyme Inhibition13m
- Irreversible Inhibition12m
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- Degree of Inhibition15m
- Apparent Km and Vmax29m
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- Competitive Inhibition52m
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- Mixed Inhibition40m
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- Recap of Reversible Inhibition37m
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- Allosteric Enzyme Conformations33m
- Allosteric Effectors18m
- Concerted (MWC) Model25m
- Sequential (KNF) Model20m
- Negative Feedback13m
- Positive Feedback15m
- Post Translational Modification14m
- Ubiquitination19m
- Phosphorylation16m
- Zymogens13m
- 8. Protein Function 9h 41m
- Introduction to Protein-Ligand Interactions15m
- Protein-Ligand Equilibrium Constants22m
- Protein-Ligand Fractional Saturation32m
- Myoglobin vs. Hemoglobin27m
- Heme Prosthetic Group31m
- Hemoglobin Cooperativity23m
- Hill Equation21m
- Hill Plot42m
- Hemoglobin Binding in Tissues & Lungs31m
- Hemoglobin Carbonation & Protonation19m
- Bohr Effect23m
- BPG Regulation of Hemoglobin24m
- Fetal Hemoglobin6m
- Sickle Cell Anemia24m
- Chymotrypsin18m
- Chymotrypsin's Catalytic Mechanism38m
- Glycogen Phosphorylase21m
- Liver vs Muscle Glycogen Phosphorylase21m
- Antibody35m
- ELISA15m
- Motor Proteins14m
- Skeletal Muscle Anatomy22m
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- 9. Carbohydrates7h 49m
- Carbohydrates19m
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- Stereochemistry of Monosaccharides33m
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- Cyclic Monosaccharides20m
- Hemiacetal vs. Hemiketal19m
- Anomer14m
- Mutarotation13m
- Pyranose Conformations23m
- Common Monosaccharides33m
- Derivatives of Monosaccharides21m
- Reducing Sugars21m
- Reducing Sugars Tests19m
- Glycosidic Bond48m
- Disaccharides40m
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- Polysaccharide7m
- Cellulose7m
- Chitin8m
- Peptidoglycan12m
- Starch13m
- Glycogen14m
- Lectins16m
- 10. Lipids5h 49m
- Lipids15m
- Fatty Acids30m
- Fatty Acid Nomenclature11m
- Omega-3 Fatty Acids12m
- Triacylglycerols11m
- Glycerophospholipids24m
- Sphingolipids13m
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- Sphingolipid Recap22m
- Waxes5m
- Eicosanoids19m
- Isoprenoids9m
- Steroids14m
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- Lipid Vitamins19m
- Comprehensive Final Lipid Map13m
- Biological Membranes16m
- Physical Properties of Biological Membranes18m
- Types of Membrane Proteins8m
- Integral Membrane Proteins16m
- Peripheral Membrane Proteins12m
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- 11. Biological Membranes and Transport 6h 37m
- Biological Membrane Transport21m
- Passive vs. Active Transport18m
- Passive Membrane Transport21m
- Facilitated Diffusion8m
- Erythrocyte Facilitated Transporter Models30m
- Membrane Transport of Ions29m
- Primary Active Membrane Transport15m
- Sodium-Potassium Ion Pump20m
- SERCA: Calcium Ion Pump10m
- ABC Transporters12m
- Secondary Active Membrane Transport12m
- Glucose Active Symporter Model19m
- Endocytosis & Exocytosis18m
- Neurotransmitter Release23m
- Summary of Membrane Transport21m
- Thermodynamics of Membrane Diffusion: Uncharged Molecule51m
- Thermodynamics of Membrane Diffusion: Charged Ion1h 1m
- 12. Biosignaling9h 45m
- Introduction to Biosignaling44m
- G protein-Coupled Receptors32m
- Stimulatory Adenylate Cyclase GPCR Signaling42m
- cAMP & PKA28m
- Inhibitory Adenylate Cyclase GPCR Signaling29m
- Drugs & Toxins Affecting GPCR Signaling20m
- Recap of Adenylate Cyclase GPCR Signaling5m
- Phosphoinositide GPCR Signaling58m
- PSP Secondary Messengers & PKC27m
- Recap of Phosphoinositide Signaling7m
- Receptor Tyrosine Kinases26m
- Insulin28m
- Insulin Receptor23m
- Insulin Signaling on Glucose Metabolism57m
- Recap Of Insulin Signaling in Glucose Metabolism6m
- Insulin Signaling as a Growth Factor1h 1m
- Recap of Insulin Signaling As A Growth Factor9m
- Recap of Insulin Signaling1m
- Jak-Stat Signaling25m
- Lipid Hormone Signaling15m
- Summary of Biosignaling13m
- Signaling Defects & Cancer20m
- Review 1: Nucleic Acids, Lipids, & Membranes2h 47m
- Nucleic Acids 19m
- Nucleic Acids 211m
- Nucleic Acids 34m
- Nucleic Acids 44m
- DNA Sequencing 19m
- DNA Sequencing 211m
- Lipids 111m
- Lipids 24m
- Membrane Structure 110m
- Membrane Structure 29m
- Membrane Transport 18m
- Membrane Transport 24m
- Membrane Transport 36m
- Practice - Nucleic Acids 111m
- Practice - Nucleic Acids 23m
- Practice - Nucleic Acids 39m
- Lipids11m
- Practice - Membrane Structure 17m
- Practice - Membrane Structure 25m
- Practice - Membrane Transport 16m
- Practice - Membrane Transport 26m
- Review 2: Biosignaling, Glycolysis, Gluconeogenesis, & PP-Pathway3h 12m
- Biosignaling 19m
- Biosignaling 219m
- Biosignaling 311m
- Biosignaling 49m
- Glycolysis 17m
- Glycolysis 27m
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- Glycolysis 410m
- Fermentation6m
- Gluconeogenesis 18m
- Gluconeogenesis 27m
- Pentose Phosphate Pathway15m
- Practice - Biosignaling13m
- Practice - Bioenergetics 110m
- Practice - Bioenergetics 216m
- Practice - Glycolysis 111m
- Practice - Glycolysis 27m
- Practice - Gluconeogenesis5m
- Practice - Pentose Phosphate Path6m
- Review 3: Pyruvate & Fatty Acid Oxidation, Citric Acid Cycle, & Glycogen Metabolism2h 26m
- Pyruvate Oxidation9m
- Citric Acid Cycle 114m
- Citric Acid Cycle 27m
- Citric Acid Cycle 37m
- Citric Acid Cycle 411m
- Metabolic Regulation 18m
- Metabolic Regulation 213m
- Glycogen Metabolism 16m
- Glycogen Metabolism 28m
- Fatty Acid Oxidation 111m
- Fatty Acid Oxidation 28m
- Citric Acid Cycle Practice 17m
- Citric Acid Cycle Practice 26m
- Citric Acid Cycle Practice 32m
- Glucose and Glycogen Regulation Practice 14m
- Glucose and Glycogen Regulation Practice 26m
- Fatty Acid Oxidation Practice 14m
- Fatty Acid Oxidation Practice 27m
- Review 4: Amino Acid Oxidation, Oxidative Phosphorylation, & Photophosphorylation1h 48m
- Amino Acid Oxidation 15m
- Amino Acid Oxidation 211m
- Oxidative Phosphorylation 18m
- Oxidative Phosphorylation 210m
- Oxidative Phosphorylation 310m
- Oxidative Phosphorylation 47m
- Photophosphorylation 15m
- Photophosphorylation 29m
- Photophosphorylation 310m
- Practice: Amino Acid Oxidation 12m
- Practice: Amino Acid Oxidation 22m
- Practice: Oxidative Phosphorylation 15m
- Practice: Oxidative Phosphorylation 24m
- Practice: Oxidative Phosphorylation 35m
- Practice: Photophosphorylation 15m
- Practice: Photophosphorylation 21m
Endocytosis & Exocytosis - Online Tutor, Practice Problems & Exam Prep
Macromolecules, such as proteins and polysaccharides, cannot diffuse through cell membranes and require endocytosis and exocytosis for transport. Endocytosis involves engulfing materials, categorized into phagocytosis (cellular eating of solids), pinocytosis (cellular drinking of liquids), and receptor-mediated endocytosis (specific pinocytosis using receptors). Exocytosis allows vesicle contents, like neurotransmitters, to exit the cell by fusing with the plasma membrane. Understanding these processes is crucial for grasping cellular transport mechanisms and their roles in biological functions.
Endocytosis & Exocytosis
Video transcript
Endocytosis & Exocytosis
Video transcript
In this video, we're going to introduce endocytosis. And really the biggest takeaway from this video is that endocytosis allows entry into the cell. Endocytosis is defined as macromolecule engulfment by the cell membrane, allowing entry into the cell as a lipid vesicle. The "en" in endocytosis can remind you of the "en" in engulfment and the "en" in entry to the cell. There are three main types of endocytosis that you should be somewhat familiar with, and we will introduce those three below. The numbers that you see above correspond with the numbers in our image below.
The first type of endocytosis is phagocytosis. Phagocytosis occurs when large and solid materials are taken up by the process of endocytosis, also known as cellular eating. It is called cellular eating because the materials that are brought in are large and solid; it's almost like the cell is eating something. The second type of endocytosis is pinocytosis. Pinocytosis occurs when small and liquid materials are taken up by the process of endocytosis, also known as cellular drinking. It is called drinking because the materials brought into the cell are small and liquid.
The third and final type of endocytosis that you should know is a specific type of pinocytosis, which is why we have this indentation to show that it is really just a subtype of the previous type. This third type is called receptor-mediated endocytosis. It is a specific form of pinocytosis that uses receptor proteins. We'll be able to see examples of each of these in our image below.
On the far left, we have an example of phagocytosis. You can see the cell's plasma membrane; the blue background represents the outside of the cell, and the other background represents the inside of the cell. During the process of phagocytosis, large and solid materials, such as an entire bacterium and multiple bacteria, can be brought into the cell, as you can see by this arrow, in the form of a lipid vesicle. Phagocytosis is a process utilized by some of our white blood cells and can be involved in immunity, essentially protecting us from harmful bacteria. Phagocytosis could also be a general process used to bring nutrients into the cell, another reason why it's referred to as cellular eating.
In the middle, we have the process of pinocytosis, and the biggest difference is the types of molecules that are brought in. Notice here what we have are very small and liquid-type materials being brought into the cell, hence it's a type of cellular drinking. The third and final type of endocytosis is receptor-mediated endocytosis. Notice that it is really just a specific type of pinocytosis. You can see that the materials are very similar, but the biggest difference is that there are receptor proteins. These orange structures embedded in the membrane as receptors are involved in the endocytotic process that allows entry into the cell.
We'll be able to get a little bit of practice with these concepts in our next video, and then we'll talk about exocytosis. So, I'll see you there.
Which of the following is FALSE about endocytotic movements?
Endocytosis & Exocytosis
Video transcript
So now that we've covered endocytosis, in this video we're going to introduce exocytosis. And really, the biggest takeaway of this video is that exocytosis allows exiting from the cell. And so exocytosis is really defined as vesicle fusion with the cell membrane allowing the vesicle contents to exit the cell into the extracellular space. And so you can think that the EX in exocytosis is for the EX in exit and the EX of extracellular space. Now many biological processes rely on exocytosis, and so neurotransmitters and zymogens of digestive enzymes are just specific examples of substances that are released by exocytosis. And so if we take a look at our image down below, notice that this here represents a cell's plasma membrane. And so over here you can see the white background represents the outside of the cell or the extracellular space. And of course, this other background over here represents the inside of the cell. And so here what you can see is that there's a vesicle filled with some cellular contents, perhaps neurotransmitters or perhaps zymogens of digestive enzymes, and this vesicle filled with contents is making its way towards the cell's plasma membrane, and ultimately what it does is it begins to fuse with the cell's plasma membrane until it is fully fused with the cell's plasma membrane and the vesicle contents are released to the outside of the cell, to the extracellular space. And so you can see here that the vesicle contents here are exiting the cell, and again, that's the biggest takeaway of this video. And so this here concludes our introduction to exocytosis and we'll be able to get some practice applying these concepts in our next couple of videos. So I'll see you guys there.
Which of the following is NOT a true statement regarding exocytosis?
Label the following phrases based on if they apply to A) Only Endocytosis, B) Only Exocytosis, or C) Both:
a) Decreases the surface area of the plasma membrane: _________.
b) Increases the surface area of the plasma membrane: _________.
c) Secretes large molecules out of the cell: _________.
d) Brings molecules into the cell: _________.
e) Requires cellular energy: _________.
Problem Transcript
Which means of particle transport is shown in the figure below?
Here’s what students ask on this topic:
What is the difference between endocytosis and exocytosis?
Endocytosis and exocytosis are cellular processes for transporting macromolecules across the cell membrane. Endocytosis involves the engulfment of materials into the cell, forming a vesicle. It includes phagocytosis (cellular eating of solids), pinocytosis (cellular drinking of liquids), and receptor-mediated endocytosis (specific pinocytosis using receptors). Exocytosis, on the other hand, involves the fusion of vesicles with the cell membrane to release their contents outside the cell. This process is crucial for the secretion of substances like neurotransmitters and digestive enzymes. Both processes are essential for maintaining cellular functions and homeostasis.
What are the three types of endocytosis?
The three types of endocytosis are phagocytosis, pinocytosis, and receptor-mediated endocytosis. Phagocytosis, or cellular eating, involves the uptake of large, solid materials like bacteria. Pinocytosis, or cellular drinking, involves the uptake of small, liquid materials. Receptor-mediated endocytosis is a specific form of pinocytosis that uses receptor proteins to selectively bring in specific molecules. Each type of endocytosis plays a unique role in cellular function and nutrient uptake.
How does receptor-mediated endocytosis differ from pinocytosis?
Receptor-mediated endocytosis is a specific type of pinocytosis that involves receptor proteins on the cell membrane. These receptors bind to specific molecules, allowing the cell to selectively take in these molecules. In contrast, pinocytosis is a non-specific process where the cell engulfs extracellular fluid and its dissolved solutes. Receptor-mediated endocytosis ensures that only target molecules are internalized, making it a more selective and efficient process compared to the general uptake in pinocytosis.
What role do fusion proteins play in exocytosis?
Fusion proteins are integral membrane proteins that facilitate the fusion of vesicles with the cell membrane during exocytosis. These proteins help the vesicle membrane merge with the plasma membrane, allowing the vesicle contents to be released into the extracellular space. This process is crucial for the secretion of substances like neurotransmitters and digestive enzymes. Fusion proteins ensure that vesicle fusion is precise and efficient, playing a vital role in cellular communication and function.
Why is exocytosis important for neurotransmitter release?
Exocytosis is essential for neurotransmitter release because it allows the vesicles containing neurotransmitters to fuse with the presynaptic membrane and release their contents into the synaptic cleft. This release is crucial for transmitting signals between neurons. Without exocytosis, neurotransmitters would not be able to exit the neuron and communicate with adjacent neurons, impairing neural communication and overall brain function.