FOM Flashcards

1
Q

Examples of locations of receptors

A
  • via plasma membrane (cell surface)
  • via intracellular receptors
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2
Q

What are parts that plasma membrane receptors commonly have?

A
  • extracellular domain, transmembrane domain, intracellular domain
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3
Q

Role of Nitric oxide in smooth muscle relaxation

A
  • acts as primary messenger in pathway
  • can act as second messenger within cells. Activates guanylyl cyclase which converts GTP to cGMP (vasodilation)
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4
Q

Examples of enzymes used in signalling

A
  • GTPases: bind to GTP to GDP
  • phosphodiesterase: breaks phosphodiester bond
  • kinase: transfer of phosphate group
  • phosphatase: hydrolysis of organic phosphate in specific environment
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5
Q

Structure of GPCRs

A
  • 7 transmembrane alpha helices spanning domain
  • specifically binds a G protein
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6
Q

What is signal amplification?

A
  • use chain of other protein messengers to amplify signal.
  • complex can activate multiple AC - cascade effect
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7
Q

Role of cAMP

A
  • activated adenylyl cyclase converts ATP to cAMP
  • transfers signals of hormones and can simulate different cell activities.
  • elicits response via protein kinase A
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8
Q

What are Tyrosine Kinase Receptors (RTK) activated by?

A
  • growth and differentiation factors or metabolic regulators
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9
Q

What occurs at RTKs at the point of ligand-binding?

A
  • form dimer. Auto/cross-phosphorylation occurs at tyrosine residues at intracellular domain
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10
Q

What does RTK autophosphorylation cause?

A
  • receptor able to recognise and activate adaptor proteins
  • activated relay proteins can then pass on signal within cell to elicit response
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11
Q

Describe MAP kinase cascade

A
  • GF binding and receptor dimerisation
  • autophosphorylation allows Grb to dock
  • binds to SOS. Complex activates RAS which activates MAPKKK- MAPKK-MAPK
  • MAPK migrates to nucleus and phosphorylates target TFs
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12
Q

Role of RAS

A
  • small G protein functioning as monomer
  • SOS transfers GTP to RAS causing activation
  • length of RAS activation depends on rate of hydrolysis of GTP to GDP
  • mutations locking RAS in active state cause many cancers
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13
Q

What do anabolic enzymes do?

A
  • building of molecules from smaller units into a larger one
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14
Q

What do catabolic enzymes do?

A
  • break down molecules into smaller units
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15
Q

What does a Michaelis-Menten plot represent?

A
  • relationship between the concentration of a substrate and the rate of the corresponding enzyme-controlled reaction
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16
Q

What does Vmax mean?

A
  • rate of reaction when enzyme is saturated with substrate
  • maximum rate of reaction
17
Q

What does Km mean

A
  • substrate conc. at which enzyme works at half its maximum rate.
  • used to compare affinity of different enzymes for their substrates
18
Q

What is a line weaver-burke plot used for?

A
  • determining Vmax and Vm of enzyme kinetics
19
Q

What comprises a nucleoside?

A
  • nitrogenous base and sugar
20
Q

What comprises a nucleotide?

A
  • nitrogenous base, sugar and phosphate
21
Q

What comprises a nucleic acid?

A
  • nitrogenous base, sugar, phosphate and phosphodiester
22
Q

How do T and U bases differ?

A
  • T on DNA, U on RNA
  • T has a methyl group
23
Q

What are two ways bases in nucleotides can be synthesised?

A
  • de novo
    -salvage
24
Q

What is the start of purine formation?

A
  • Ribose-5-phosphate which derives from pentose phosphate pathway
25
Q

How is PRPP formed?

A
  • Ribose-5-phosphate is converted into PRPP by PRPP synthesise
26
Q

What happens in the reaction of PRPP with glutamine?

A
  • glutamine donates one amide group to carbon 1 to form 5-phosphoribosylamine
27
Q

What atoms are sequentially added to build the purine ring?

A
  • glutamine
    -aspartate
  • CO2
28
Q

What is the first fully formed purine nucleotide in the de novo pathway?

A
  • IMP, inosine monophosphate
29
Q

Describe feedback inhibition in purine formation

A
  • ensures balance in purine synthesis
  • AMP and GMP inhibit early steps of pathway.
    -Cross-regulation
30
Q

Describe the salvage pathway of purine formation

A
  • recovers purine from normal cell turnover and converts to nucleoside triosphosphate
31
Q

What enzymes are involved in the salvage pathway of purine formation?

A
  • HGPRT: converts hypoxanthine to IMP and guanine to GMP
  • APRT: converts adenine to AMP
32
Q

What is the only purine nucleoside to be salvaged?

33
Q

Importance of deoxyribonucletides in nucleotides synthesis

A
  • ribonucleotide reductase converts ribonucleotides to deoxyribonucletides
  • Feedback inhibition occurs when dATP is formed
34
Q

How is orotate produced in pyrimidine formation?

A
  1. glutamine, CO2, ATP, aspartate and tetrahydrofolate required in forming pyrimidine ring
  2. carbamoyl aspartate is oxidised to form orotate
35
Q

How does the attachment of pyrimidine ring to ribose-5-phosphate occur?

A
  • PRPP provides ribose sugar
  • reacts with orotate to form OMP
  • enzyme PRPP synthetase converts ribose to PRPP