cell membranes Flashcards

1
Q

describe the characteristics phospholipids

A
  • glycerol + phosphate head + fatty acid chains (lipid tails)
  • amphipathic molecule: non-polar end (hydrophobic tails) and polar end (hydrophilic heads)
  • bilayer: two layers, in water polar heads seek partners for hydrogen bonding and non-polar tails pack together
  • selectively permeable, permeability of molecule affected by lipid solubility, size and charge
  • permeable: gases, water, small uncharged polar molecules
  • impermeable: charged polar (AA and ATP), ions, large uncharged polar molecules
  • fluidity: degree of alignment of tails, cholesterol inserter amongst = maintain fluidity at low temperature
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2
Q

describe the movement of substances (diffusion) across a membrane

A
  • simple: random thermal motion of substances from regions of high concentration to regions of lower concentration
  • conc. gradient: difference in conc. of a substance
  • movement direction: high to low, with gradient towards equilibrium
  • electrochemical gradient: electrical potential gradient,, +ve ions attracted to -ve ions, vice versa, not linked to number of particles as 1 -ve and 1 +ve = 0, 6+ve and 6-ve = 0
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3
Q

describe the different types of cell membrane proteins

A
  • integral (1): transmembrane proteins
  • peripheral (2): attachment to network of supporting fibres, exterior glycoproteins / glycolipids
  • transporters: channels to allow flow (active pumps)
  • enzymes: catalyse reactions in cytoplasm (often clustered, work as a team)
  • cell surface receptors: binding site with specific shape for messenger chemical (hormone)
  • cell surface identity markers: glycoprotein ‘tags’
  • cell adhesion markers: junction formation between cells
  • cytoskeleton and extracellular attachments: provide support and shape while transmitting messages
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4
Q

describe protein assisted transport

A
  • passive (facilitated, gradient is favourable but rate is too slow)
  • active (unfavourable gradient)
  • channels: hydrophilic pores through membrane, not coupled with energy usage, ions diffuse down electrochemical gradient
  • carriers: interaction between molecule / carrier protein, passive / active, radical conformational change, slower than channels
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5
Q

what is osmosis

A
  • net movement of water across a membrane, rapidly moves across selectively permeable membrane
  • through bilayer and aquaporins (channels)
  • move from high energy (low solute) to low energy (high solute)
  • hypertonic: more solute, dilute, water leaves cell = shrinks
  • hypotonic: less solute, concentrated, water enters = cell bursts / lysis
  • isotonic: same concentrations, cell fluctuates about equilibrium
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6
Q

what is active transport

A
  • pumping solutes across a membrane against their concentration gradient
  • primary AT: carrier protein pumps use energy directly
  • essential to maintain required solute conc. in animal cells
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7
Q

describe the NaK pump

A
  • active movement
  • high K inside (overall -ve charge) and high Na outside
  • area of protein is non-polar to allow it to sit embedded in membrane
  • anchored due to chemical relationship
  • affinity: becomes more receptive to either Na or K, changes in shape of receptor sites (domains) in conjunction with these changes
  • phosphorylates: ATP to ADP, release and transfer energy to protein, allows Na to be moved against gradient
  • 3 Na out and 2 K in (net loss, hence inside if -ve)
  • resting membrane potential = difference in charge (-70mV)
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8
Q

what is co transport

A
  • coupling transport of two solutes (secondary active transport
  • accumulates molecules within cells against a gradient
  • harness energy from Na or H moving down their conc. gradients
  • sugars, AA, transverse up gradient
  • use energy from first movement
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9
Q

describe co transport of glucose via symport

A
  • entering / exiting cell from the same side
    1. H pumped out of cell (active)
    2. conc. gradient favours re-entry of H (passive)
    3. H and sugar bind to symport simultaneously on same side of membrane, H moves down gradient (passive) and sugar moves up gradient (active)
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10
Q

describe go transport via antiports

A
  • counter transport, enter / exit cell from opposite side of protein
  • inward movement of Na coupled with outward movement of solute
  • both simultaneously bind to anti port on opposite sides of membrane
  • energy captured by Na moving down gradient is used to move solute up its own gradient
  • one substance can be transported by many proteins
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11
Q

what is cystic fibrosis

A
  • genetic disorder
  • affect cell singing in lungs. / pancreas, thick sticky mucous, high Cl
  • abnormal or absent Cl channels, high extracellular Cl
  • daily exercise, strong antibiotics, digestive enzymes, synthesised molecule (reduce symptoms)
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12
Q

how is bulk matter moved throughout cells

A
  • endocytosis: movement in, plasma membrane extends outwards and envelopes food particles (vesicles), phagocytosis (food), pinocytosis (liquid), receptor mediated
  • exocytosis: outward movement, discharge of material from vesicles at cell surface
  • transcytosis: endocytosis directly followed by exocytosis (cell uses what is valuable and discharges what is not from cell)
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13
Q

what is a neuron

A
  • specialised nerve cell
  • receive, process and send information
  • dendrites (receive), cell body (soma), axon (carries output signal)
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14
Q

what is action potential problem and solution

A
  • long distance electrical signalling
  • problem: due to resistance, the amplitude of an electrical impulses fades the further it travels
  • solution: action potential prevent loss / distortion of signal because they are regenerated, all or none response, long distance transmission, voltage gated channels are key to this mechanism (NaK)
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15
Q

what are gated channels

A
  • open and close in response to stimuli
  • chemically ligand: binding of messenger (neurotransmitter)
  • voltage gated: change in electrical potential of membrane
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16
Q

describe neurons and electrical signals / stimuli

A
  • stimuli: neuron is stimulated, polarising / depolarising of cell membrane to different degrees depending on magnitude of stimulus
  • action potential: not generated until threshold is reached (-55mV)
17
Q

what is resting neuron potential and what occurs when it is stimulated

A
  • cell -ve inside and +ve outside (resting = -70mV)
  • polarity: dependent on Na K pumps, anions inside cell and low permeability to their loss (Na K leak channels, more K leakage = -ve charge)
18
Q

describe the process of action potentials

A
  1. resting state: Na K gated channels are closed
  2. depolarisation: stimulus leads to few Na+ gated channels open and Na+ rushes into the cell
  3. trigger = threshold (-55mV) if it doesn’t the membrane returns to resting state
  4. rapid depolarisation (rising phase): more Na+ channels open, triggers
    repolarisation
  5. (falling phase): Na+ channels inactivate (inflow ceases), K+ channels open and outflow begins
  6. repolarisation of the membrane, potential falls
  7. hyper-polarisation (undershoot): Na+ channels close, K+ channels remain open, potential falls below the resting state (-80 mV)
  8. resting state: sodium potassium pump returns the membrane to a polarised state via active transport)
19
Q

what is a synapse / NMJ

A
  1. action potential arrives at axon terminal of pre-synaptic cell, depolarising the presynaptic membrane
  2. depolarisation opens voltage gated channels, triggering an influx of Ca ions
  3. elevated Ca concentration causes synaptic vessels to migrate towards and fuse with the presynaptic membrane
  4. vesicles release neurotransmitter into the synaptic cleft via exocytosis (chemical messenger)
  5. neurotransmitter diffuses across synaptic cleft
    1. neurotransmitters bind to ligand gated ion channels in the postsynaptic membrane and generate an electric current to depolarise the postsynaptic neuron
    1. neurotransmitter binds to ligand gated channels on muscle and trigger contraction
20
Q

what are two ways you can interfere with impulses

A
  • botox: prevents vesicles in pre-synaptic membrane from forming a connection with membrane, no neurotransmitter released
  • tetredotoxin: paralyses signal, no rest, stimulus is continuous, prevents normal breakdown of ACh, involuntary muscle contraction, respiratory / cardiac arrest
21
Q

what is the refractory period

A
  • when a neuron is stimulated it cannot be stimulated by another stimuli
  • inactivated during depolarisation and repolarisation phases