Exam Questions Jan Exam Flashcards
The muscle fibre is relaxed. When the muscle contracts what happens to the appearance of:
- A band
- I band
- H zone
A: no change
I: shorter
H: shorter/disappears
Describe the role of calcium ions in muscle contraction (2)
Binds tropomyosin filaments
Revealing binding sites on actin activating ATPase
Skeletal muscle is made of bundles of fibres.
a) Describe the roles of calcium ions, ATP and phosphocreatine in producing contraction of a muscle fibre. (4
Calcium ions bind to troponin;
Remove blocking action of tropomyosin / exposes actin binding sites;
ATP allows myosin to join / bind to actin / form cross-bridge;
‘Re-cocks’ myosin cross bridge / allows detachment from actin;
Enables calcium ions to be pumped back in;
Phosphocreatine allows regeneration of ATP without respiration;
Phosphocreatine releases Pi to join ADP;
Endurance athletes, such as marathon runners, nearly always have a high proportion of slow fibres in their muscles. Explain the benefit of this.
Endurance athletes exercise for long periods of time; Respire / release energy aerobically; Or too much lactate would accumulate; Slow twitch fibres adapted to aerobic metabolism; As have many mitochondria; Site of Krebs’ cycle; And electron transport chain; Much ATP formed; Also are resistant to fatigue;
Both slow and fast fibres contain ATPase. Explain why (2)
Splitting / breakdown / hydrolysis of ATP; (Muscle) contraction requires energy / ATP;
Use of ATP by myosin.
The muscle in the diagram had been stained for viewing with a microscope.
What is the evidence that it had been stained for viewing with an optical microscope? (2)
- 2.
3.
Accept either approach as some texts refer to ATPase as the enzyme at the end of the ETC in mitochondria.
Need light to see colour / brown / yellow;
Requires reference to light.
Cannot see colour / brown / yellow with electrons / an electron microscope;
Requires reference to electrons / electron microscope.
Accept ‘see black and white with electrons / electron microscope’.
No organelles are visible.
Accept appropriate named examples of organelles.
One form of muscle disease is caused by a mutated allele of a gene. This leads to production of myosin molecules that are unable to bind to other myosin molecules.
If myosin molecules are unable to bind to other myosin molecules, this prevents muscle contraction.
Use the diagram and your knowledge of how muscles contract to suggest why. (3)
Can’t form myosin / thick filaments;
Neutral: prevents actin and myosin sliding filament action
Can’t pull / can’t move actin / slide actin past / (myosin) have to be joined / fixed to pull actin;
Accept: myosin can’t pull on each other
Myosin moves / if attached doesn’t move;
Can’t move actin towards each other / middle of sarcomere / between myosin / can’t shorten sarcomere / can’t pull Z lines together.
Describe the roles of calcium ions in the contraction of a myofibril (5)
Calcium ions diffuse into myofibrils from (sarcoplasmic) reticulum; (Calcium ions) cause movement of tropomyosin (on actin);
(This movement causes) exposure of the binding sites on the actin; Myosin heads attach to binding sites on actin;
Hydrolysis of ATP (on myosin heads) causes myosin heads to bend; (Bending) pulling actin molecules;
Attachment of a new ATP molecule to each myosin head causes myosin heads to detach (from actin sites
What’s the role of phosphocreatine in providing energy during muscle contraction? (2)
To make ATP;
Accept:
ADP + CP → ATP + C Neutral – provides ATP
People who have McArdle’s disease produce less ATP than healthy people. As a result, they are not able to maintain strong muscle contraction during exercise. Use your knowledge of the sliding filament theory to suggest why. (3)
(Idea ATP is needed for:)
1. Attachment / cross bridges between actin and myosin;
Accept the role of ADP in attachment
2. ‘Power stroke’ / movement of myosin heads / pulling of actin;
Not just ‘filaments slide’ as given in the question stem
3. Detachment of myosin heads;
4. Myosin heads move back / to original position / ‘recovery stroke’
Explain how the resting potential of -70 m is maintained in the sensory neurone when no pressure is applied.
The nembrane is less permeable to sodium ions but more permeable to potassium ions. This means that sodium ions are pumped out whilst potassium ions are pumped in.
Explain how applying pressure to the Pacinian corpuscle produces the changes in membrane potential recorded by microelectrode p
Pressure causes the membrane to become stretched, so.sodium.ion channels in the membrane open and sodium ions move in. More channels open when the pressure is greater.
Both slow and fast muscle fibres contain ATPase. Explain why (2)
Splitting / breakdown / hydrolysis of ATP;
(Muscle) contraction requires energy / ATP;
The tissue in the diagram came from muscle with a high proportion of brown-staining fibres. Was the tissue removed from slow or fast skeletal muscle?
Explain your answer. (1)
Fast because (lots of) ATPase allows rapid hydrolysis of ATP OR Slow because (lots of) ATPase allows rapid synthesis of ATP.
Damage to the myelin sheaths of neurones can lead to problems controlling the contraction of muscles.
Suggest one reason why.
Action potentials travel more slowly/don’t travel
So delay in muscle contraction/ muscle don’t contract
ORRR
Action potential/depolarisation leaks to adjacent neurones
So wrong muscle fibres contract