Haemoglobin And Myoglobin Flashcards

1
Q

Oxygen binding in myoglobin

A

Shows a hyperbolic dependence on oxygen concentration

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2
Q

Haemoglobin structure

- binds to 4O2 molecules

A

2 alpha and 2 beta polypeptide chains in a tetramer
Each chain contains the haem prosthetic group
Oxygen binding to on subunit causes a conformational change in the other subunits from low affinity T state to high affinity R state

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3
Q

Oxygen binding in Haemoglobin

A

binding of 1 O2 increases the affinity of the other subunits to oxygen - cooperative binding gives a sigmoidal curve (T-R state)
This means O2 can efficiency be carried from the lungs to the tissues

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4
Q

2,3-Bisphosphoglycerate

2,3-BPG

A

1 BPG per tetramer
Decreases the affinity for O2
BPG concentration increases at high altitudes - promotes the release of O2 at the tissues

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5
Q

The BOHR effect

A

H+ and CO2 can bind to Hb - lowers the affinity of Hb for oxygen (curve shifts to the right)
Metabolically active tissues produce large amounts of H+ and CO2 - ensures delivery of O2 is coupled to demand

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6
Q

Carbon Monoxide Poisoning

CO

A

Binds to Hb 250x more readily than O2 does
Increases the affinity for oxygen of the subunits it is not bound to - oxygen is not released at tissues
Irreversible binding - fatal if >50% of the subunits are bound to CO

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7
Q

Foetal Haemoglobin

HbF

A

Has a higher binding affinity for O2 than HbA - allows the transfer of O2 into the foetal blood supply from the mother

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8
Q

Myoglobin Structure

- binds to 1O2 molecule

A

153aa
75% alpha helical
Oxygen binding causes movement of Fe into the plane of the ring - small change in overall protein conformation

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9
Q

Sickle cell anaemia

HbS

A

Mutation of Glutamate to Valine in beta globin
Hydrophilic aa to hydrophobic aa - they clump together
More prone to lyse - anaemia
More rigid - block microvascular

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10
Q

Thalassaemias

Imbalance between number of alpha and beta chains

A

Beta thalassaemia - only has alpha chains - symptoms appear after birth (6 months when gamma chains supposed to change to beta chains) unable to form stable tetramers

Alpha thalassaemia - only has beta chains, onset before birth (severity depends on number of alpha chains) beta chains can form stable tetramers with and increased affinity for oxygen

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