1.3 Membrane Structure Flashcards
membrane structure essential idea
The structure of biological membranes make them both fluid and dynamic
Phospholipid
Lipid where one fatty acid is replaced by a phosphate group, in membranes characterized by phosphate (polar) head and lipid (non polar) tails
Hydrophilic
Polar/ charged unit that is attracted to water
Hydrophobic
Non polar unit that is repelled by water
Phospholipid emergent properties
When put into water, an emergent property is that phospholipids self-organize to keep heads wet and tails dry
Amphipathic
Molecule made form bio the hydrophilic and hydrophobic subunits
Phospholipid movement
Phospholipids flow past each other laterally but can’t move vertically
Integral proteins
Permanently embedded proteins that go all the way through membranes. They are
Integral protein
Protein thats permanently embedded in the cell and goes all the wya through, penetrating one surface (mono topic), or many surfaces (poly-topic). Integral proteins are amphipathic.
Glycoproteins/ glycolipids
Proteins with oligosaccharide (few sugar) chain attached, used for cell recognition by immune system and as hormone receptors
Peripheral proteins
Temporary association with cell membrane, polar molecules that reside on the outside of the membrane
Protein functions
Transport, receptors, anchorage, cell recognition, intercellular joining, enzymatic activity
Role of cholesterol in cell membrane
Makes phospholipids pack more tightly and regulates fluidity and flexibility of the membrane by providing structure and rigidity as well as regulating permeability to hydrophilic molecules
Attachment to membrane
Hydroxyl group makes the head of the molecule hydrophilic and attracted to phosphate heads on membrane periphery. The hydrophobic tail attracts to lipid tails within the membrane
Describe the nature of membrane fluidity
Maintained in mammalian membranes by cholesterol as the hydrophobic tails behave as a liquid while the phosphate head behaves as a solid, making the membrane neither solid nor liquid but fluid
Why should membrane fluidity be regulated
Fluidity required for cell movement and material exchange, however overly fluid membranes cannot effectively regulate and restrict the movement of substances in and out of the cell
Cholesterol and Fluidity
Presence of cholesterol in membranes restricts phospholipid movement and therefore reduces fluidity
Cholesterol and fluidity in cold temperatures
The presence of cholesterol prevents crystallization and solidification at cold temperatures, therefore increasing fluidity by disrupting regular packing of hydrocarbon tails
Description of the Singer-Nicholson Fluid Mosaic Model
Considered the most accurate model to date. Phospholipids form a bilateral that is fluid and moves laterally. The membrane also consists of proteins that can be either peripheral or integral. The membrane is a fluid mosaic of phospholipids and proteins. Proposed in 1972.
Evidence of the singer-Nicholson model as opposed to davson-danielli model
Membranes proteins were found to be globular and varied in size so they would be unable to form a continuous layer on the membranes periphery. Membrane proteins also has hydrophobic tendencies, suggesting they would embed within the membrane as opposed to outside of it.
Davson-Danielli model
A phospholipid membrane surrounded by a layer of protein on either side
Evidence of the Davson-Danielli model
High magnification electron microscopes show membranes appearing as two dark lines with lighter space in-between, leading to the belief that proteins surrounded the phospholipid bilayer as proteins are darker beneath the microscope.
Falsification of the Davson-Danielli model through freeze fracturing
Freeze fracturing that demonstrated fractures along lines of weakness including the center of the membrane. The fracture also revealed an irregular and rough surface within the bilayer with globular structures that were then interpreted as trans-membrane proteins
Falsification of Davson-Danielli model through flourescent antibody tagging
Red and green fluorescent markers attached to the antibodies that bind to membrane proteins. Within 40 minutes the red and green proteins had mixed throughout the membrane, showing that proteins were not fixed to the peripheral layer
Calculating magnification
Scale bar measurement / scale bar label
Calculating actual size
Measured length / magnification
Shortcomings of the davson-danielli membrane model
- assumed all membranes had an identical structure which didn’t;t explain how different membranes had different functions
- proteins are amphipathic though largely non polar and hydrophobic, making it strange for them to be situated on periphery of membrane