Lecture 13: Membranes, Organelles, Cytoskeleton Flashcards
Lysosomes
Single layer vesicles with acidic lumen containing enzymes for breakdown of biochemical macromolecules, endocytosed material, and old organelles. Primary site of proteolysis.
Lysosomal storage diseases
Caused by sphingolipid buildup in lysosomes due to inability to break down, e.g. Tay-Sachs disease
Peroxisomes
Single layer vesicles carrying hydrogen peroxide, responsible for beta-oxidation of cellular lipids and synthesis of some glycolipids
Spherocytes
RBCs shaped as spheres; due to hereditary spherocytosis leading to hemolytic anemia
Major plasma membrane lipids
- Glycerophospholipids
- Sphingolipids
- Cholesterol
How does cholesterol affect the lipid bilayer?
Its steroid rings partially immobilize the FA tails of phospholipids, creating stiffer membranes and regulating membrane fluidity
How does cholesterol regulate membrane fluidity?
“Anti-freeze” effect; at cold temperatures, cholesterol prevents phospholipids from condensing too much and freezing. At hot temperatures, cholesterol holds phospholipids together, preventing dissolution.
Types of membrane protein
- Integral
- Peripheral
Integral membrane proteins
Proteins that cross both layers of a phospholipid bilayer
Peripheral membrane proteins
Proteins that only interact with one layer of a phospholipid bilayer
What causes atypical “walking” pneumonia?
Mycoplasma consume membrane cholesterol, increasing membrane fluidity leading to limp cilia. Mucus accumulation provides a growth medium for more bacteria.
Factors that affect membrane fluidity
- Temperature (hotter = more fluid)
- FA chain length (longer = less fluid)
- Unsaturation (more = more fluid)
- Cholesterol (more = less fluid)
Liposomes
Small artificial vesicle with phospholipid bilayer; materials can be embedded in the membrane or within the lumen. Often used for targeted drug delivery.
Main components of the cytoskeleton
- Actin
- Microtubules
- Intermediate filaments
Microtubule structure
αβ tubulin heterodimers form long cylinders of non-covalent αβ polymers (protofilaments), which assemble laterally into microtubules (~13 proto-f in mammals). Capping proteins stabilize ends and nucleated at centrosome from (-) end.
Different types of tubulin
α-tubulin: towards (-) end (slower growing end)
β-tubulin: towards (+) end (faster growing end)
γ-tubulin: template for correct assembly
How are microtubules regulated?
Various proteins for assembly, stabilizing, destabilizing, cutting, and motor movement (kinesin +, dynein -).
Also tubulin isoforms, post-trans. mods
Microtubule therapeutics
Taxol (stabilizes microtubules), colchicine (inhib. polymer.), vinblastine (inhib. polymer.); these stop cell function by preventing microtubule growth.
Intermediate filament structure
α helical monomer -> coiled coil dimer -> staggered tetramer -> 2 packed tetramers, staggered -> 8 tetramers twisted into a filament
Intermediate filament roles
Mechanical integrity, sequester/position/scaffold signaling molecules
Actin structure
Double stranded helical polymers of monomeric actin forming linear bundles, 2D networks, and 3D gels with faster growing (+) end and slower growing (-) end
Types of actin monomer
- α
- β
- γ
Each actin filament has only 1 type of actin