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U2.2_B2.1 Membrane and Transport

SEK CIUDALCAMPO

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B2.1 Membrane and transportD2.3 Water Potential

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In this unit we will be able to see characteristics of the cell membrane and how to transport things across it!

go!

Título 2

B2.1.1— Lipid bilayers as the basis of cell membranes.

Subtítulo

B2.1.1— Lipid bilayers as the basis of cell membranes.

Membrane-bound organelles

B2.1.2— Lipid bilayers as barriers.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Interior is non-polar and hydrophobic!

B2.1.4— Integral and peripheral proteins in membranes.

B2.1.4— Integral and peripheral proteins in membranes.

Integral Proteins Integral proteins penetrate the phospholipid bilayer to remain permanently attached to the membrane These transmembrane proteins cannot be readily isolated without disrupting the bilayer (e.g. via detergents) Examples of integral membrane proteins include glycoproteins, ion channels, carrier proteins and protein pumps

B2.1.4— Integral and peripheral proteins in membranes.

Integral Proteins Integral proteins penetrate the phospholipid bilayer to remain permanently attached to the membrane These transmembrane proteins cannot be readily isolated without disrupting the bilayer (e.g. via detergents) Examples of integral membrane proteins include glycoproteins, ion channels, carrier proteins and protein pumps

B2.1.4— Integral and peripheral proteins in membranes.

B2.1.9— Structure and function of glycoproteins and glycolipids..

B2.1.9— Structure and function of glycoproteins and glycolipids..

B2.1.9— Structure and function of glycoproteins and glycolipids..

Glycoproteins and glycolipids also play an important role in maintaining the structural integrity of the extracellular matrix The extracellular matrix is a network for external molecules that provide structure and biochemical support to surrounding cells The carbohydrate chains can link these extracellular molecules together to help make the matrix a cohesive network

B2.1.9— Structure and function of glycoproteins and glycolipids..

B2.1.10— Fluid mosaic model of membrane structure.

Cell membranes are represented according to a fluid-mosaic model, due to the fact that they are: Fluid – the phospholipid bilayer is viscous and individual phospholipids can move position Mosaic – the phospholipid bilayer is embedded with proteins, resulting in a mosaic of components

B2.1.10— Fluid mosaic model of membrane structure.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Título 2

B2.1.3— Simple diffusion across membranes.

Solutes diffuse from a region of higher solute concentration to a region with lower solute concentration through the membrane.

Simulation:

B2.1.3— Simple diffusion across membranes.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

B2.1.3— Simple diffusion across membranes.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

B2.1.3— Simple diffusion across membranes.

B2.1.6— Channel proteins for facilitated diffusion.

Facilitated diffusion is the passive movement of molecules across the cell membrane via the aid of a membrane protein It is utilised by molecules that are unable to freely cross the phospholipid bilayer (large, polar molecules and ions) This process is mediated by two distinct types of transport proteins – channel proteins and carrier proteins

B2.1.6— Channel proteins for facilitated diffusion.

Channel Proteins Integral lipoproteins which contain a hydrophilic pore via which ions may cross from one side of a membrane to the other Channel proteins are ion-selective and may be gated to regulate the passage of ions in response to certain stimuli Channel proteins only move molecules along a concentration gradient (i.e. are not used in active transport) Channel proteins have a much faster rate of transport than carrier proteins

B2.1.6— Channel proteins for facilitated diffusion.

Carrier Proteins Integral glycoproteins which bind a solute and undergo a conformational change to translocate the solute across the membrane Carrier proteins will only bind a specific molecule via an attachment similar to an enzyme-substrate interaction When a carrier protein moves material against the gradient (using ATP hydrolysis) it is called a protein pump Carrier proteins have a much slower rate of transport than channel proteins (by an order of ~1,000 molecules per second)

B2.1.7— Pump proteins for active transport.

Active transport implies the use of ATP (energy) in order to move molecules from one side to the other

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D2.3.1 — Solvation with water as the solvent.

D2.3.1 — Solvation with water as the solvent.

Water can form hydrogen bonds with other molecules, making "water shells with them.

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Water can form hydrogen bonds with other molecules, making "water shells with them.

B2.1.5— Movement of water molecules across membranes by osmosis and the role of aquaporins.

Water diffuses from a region of lower solute concentration (and higher water concentration) to a region with higher solute concentration (and lower water concentration) through the membrane.

B2.1.5— Movement of water molecules across membranes by osmosis and the role of aquaporins.

Aquaporins Help water move through the internal hydrophobic part of the phospholipid bilayer Discovered by Peter Agre and colleagues

https://pubmed.ncbi.nlm.nih.gov/1373524/

D2.3.2—Water movement from less concentrated to more concentrated solutions D2.3.3—Water movement by osmosis into or out of cells

Water is always moving in and out of the cell, even in isotonic solutions

D2.3.2—Water movement from less concentrated to more concentrated solutions D2.3.3—Water movement by osmosis into or out of cells

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

Esto es un párrafo listo para contener creatividad, experiencias e historias geniales.

D2.3.2—Water movement from less concentrated to more concentrated solutions D2.3.3—Water movement by osmosis into or out of cells

D2.3.2—Water movement from less concentrated to more concentrated solutions D2.3.3—Water movement by osmosis into or out of cells

Contractile Vacuoles Unicellular organisms (such as protists) may possess a contractile vacuole to regulate the osmotic conditions within the cell Excess water is absorbed into the contractile vacuole, causing it to swell (this is called diastole) The vacuole then fuses to the plasma membrane and contracts, expelling the water (this is systole) The amount of water expelled and the rate of contractions are determined by the extracellular conditions

D2.3.2—Water movement from less concentrated to more concentrated solutions D2.3.3—Water movement by osmosis into or out of cells

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Título 2

D2.3.7—Medical applications of isotonic solutions

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B2.1.11— Relationships between fatty acid composition of lipid bilayers and their fluidity

B2.1.11— Relationships between fatty acid composition of lipid bilayers and their fluidity

Unsaturated fatty acids have double bonds in their lipid chain which results in a kinked hydrocarbon tail This means the lipids are harder to pack together, lowering their viscosity (and increasing fluidity) Unsaturated fatty acids in lipid bilayers also have lower melting points, so membranes are more fluid and flexible at temperatures experienced by a cell.

B2.1.11— Relationships between fatty acid composition of lipid bilayers and their fluidity

Saturated fatty acids have no double bonds in their lipid chain which results in a straight hydrocarbon tail This means the lipids will be easier to pack together, increasing their viscosity (and lowering fluidity) Saturated fatty acids have higher melting points and make membranes stronger and more stable at higher temperatures

B2.1.11— Relationships between fatty acid composition of lipid bilayers and their fluidity

B2.1.11— Relationships between fatty acid composition of lipid bilayers and their fluidity

B2.1.12— Cholesterol and membrane fluidity in animal cells

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B2.1.11— Membrane fluidity and the fusion and formation of vesicles

Exocytosis Endocytosis

B2.1.11— Membrane fluidity and the fusion and formation of vesicles

B2.1.11— Membrane fluidity and the fusion and formation of vesicles

Subtítulo

B2.1.15— Sodium–potassium pumps as an example of exchange transporters

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n example of antiport is the translocation of sodium and potassium ions by the sodium-potassium pump This pump is used by nerve cells (neurons) to establish an electrochemical gradient across the membrane (resting potential)

B2.1.16— Sodium-dependent glucose cotransporters as an example of indirect active transport

In this case, a molecule of Na+ is necessary to introduce a molecule of glucose in the cell. That molecule, then, goes to the Na+/K+ pump to re-balance the ions

B2.1.17— Adhesion of cells to form tissues

Cell adhesion is the attachment of cells to other cells or to the extracellular matrix via specialised membrane proteins called cell adhesion molecules (CAMs) There are different forms, depending on their function.

B2.1.17— Adhesion of cells to form tissues