Cell Membrane, Part 2 Flashcards
- structure of a biological membrane - concept of membrane fluidity - ECM and its function in cell physiology
membrane dynamics
- flexibility: ability to change shape without losing integrity or becoming leaky
- basis for this are non covalent interactions among lipids in the bilayer (thus, mobility)
- structure and flexibility of bilayer depend on kinds of lipids present
- changes with temperature
vesicle
- intracellular structures consisting of liquid enclosed in lipid bilayer
- form naturally during:
- secretion (exocytosis)
- uptake (endocytosis)
- membrane transport
liposomes
- synthetic spherical bilayers vesicles
- model membranes in experimental studies
black membranes
- planar bilayers
- formed across a hole in a partition btwn 2 aqueous compartments
- used to measure permeability properties of synthetic membranes
cell membrane fluidity
- movement of phospholipids within lipid bilayer
transversal diffusion
- flip-flop
- happens rarely
lateral diffusion
- happens readily and rapidly
flippases and floppases
- need ATP
scramblases
- does not need ATP
- special transport proteins move phospholipid and other lipids in the membrane
lipid bilayer
- fluidity must be precisely regulated
- depends on its composition and temperature
- stabilized by hydrophobic interactions btwn lipids’ fatty acid chains
phase transition
- change of a lipid bilayer from a liquid to a 2-D rigid crystalline state (gel) at a characteristic temperature
- phase transition and temp at which this occurs is lower if phospholipid chains are short or have double bonds
fluidity depends on:
- lipid composition
- more cis-double bonds -> more fluid
- double bonds make it difficult to pack chains together
- more spread apart -> form a thinner membrane
- shorter chain: reduces tendency of hydrocarbon tails to interact with one another -> membrane remains fluid at lower temps
- more cis-double bonds -> more fluid
- cholesterol content
- temperature
- at low temps, lipids show less movement
- lipid is in paracrystalline state (more rigid state)
- at higher temps (20-40C), plasma membrane becomes more fluid
saturated fatty acids
- tend to form paracrystalline structures (less space btwn phospholipid tails
- the more saturated fatty acids a lipid bilayer contains, the higher the paracrystalline-to-fluid transition temp of a membrane
unsaturated fatty acids
- yields to formation of kinks -> inhibits paracrystalline conformation (more space btwn tails)
lipid bilayer components
- also contains cholesterol and glycolipids
- eukaryotic plasma membranes contain large amounts of cholesterol
- cholesterol molecules improve permeability-barrier properties of lipid bilayer
- orient themselves with hydroxyl groups close to polar heads of phospholipid molecules
- rigid steroid ring can support hydrocarbon chains and stabilize them
- inhibits possible phase transitions
cholesterol
- orients itself in bilayer with its small hydroxyl groups close to the polar head groups of adjacent phospholipids and the hydrophobic chain btwn phospholipid tails (hydrophobic interaction)
- helps keep membrane more stable, stiffening bilayer and making it less fluid and less permeable
- stops tails from clumping and interacting
- helps membrane remain fluid
cell membrane transport
- passive transport
- transporters or permeases
passive transport
- simple diffusion
- facilitated diffusion
- electrochemical gradient
- channels
transporters or permeases
- carriers
- active transporters
- pumps
- symport systems
extracellular matrix (ECM)
- complex and intricate network of macromolecules
- provides structural and biochemical support to surrounding cells
- common functions:
- cell adhesion, cell-cell communication and differentiation
- animal ECM includes: interstitial matrix and basement membrane/basal lamina
interstitial matrix
- present btwn diff animal cells (in intercellular spaces)
- gels of polysaccharides and fibrous proteins fill intercellular spaces -> act as compression buffer to ECM
basement membrane
- sheet-like depositions of ECM with epithelial cells
connective tissue with respective type of ECM
- bone tissue: collagen fibers and bone mineral
- loose connective tissue: reticular fibers and ground substance
- blood: ECM is blood plasma
extracellular matrix
- macromolecules in ECM produced locally by cells in the matrix and secreted via exocytosis
fibroblasts
- in connective tissue (collagen fibers)
- secrete ECM
- chondroblasts - cartilage
- osteoblasts - bone tissue
major classes of macromolecules in ECM
- mammals have >300 matrix proteins
1. glycosaminoglycans (GAGs, ex: cartilage): large and highly charged polysaccharides- when linked to proteins -> proteoglycans
- fibrous proteins: like collagen (ex: skin and bone)
- non-collagen fibrous proteins: such as glycoproteins (elastin, fibronectin, laminin)
- when linked to proteins -> proteoglycans
collagen
- fibrous, long, stiff, triple-stranded helical proteins
- ‘fibrils’ rich in proline and glycine and glycosylated
types of collagen and their properties
Type I: fibril-forming (fibrillar)
- bone, skin, tendons, ligaments, cornea, internal organs (accounts for 90% of body collagen)
Type III: fibril-forming (fibrillar)
- skin, blood vessels, internal organs
Type IV: network-forming
- basal lamina
Elastin
- gives tissues their elasticity (skin, blood vessels, lungs)
- hydrophobic protein rich in proline and glycine (like collagen) but is NOT glycosylated
- molecules are joined together by strong covalent bonds to generate a cross-linked network
- each elastin molecule can extend and contract resembling a random coil, so entire assembly can stretch and recoil like a rubber band
In ECM there are also glycoproteins
- with multiple domains each with specific binding sites for other matrix macromolecules and for receptors of the cell surface
- ex: Fibronectin (2500 AAs long) helps organize ECM and cells attached to it
basal lamina
- aka basement membrane
- specialized form of ECM
- thin, flexible, tough -> essential component of all epithelia
laminin
- primary organizer of sheet structure of basal lamina
- composed of 3 long polypeptide chains held together by DISULFIDE BONDS
- multi domain protein
- asymmetric molecule
integrins
- transmembrane cell adhesion proteins
- act as ‘matrix receptors’
- link cytoskeleton with ECM