The Cross Bridge Cycle
Trending Questions
A. Large and more numerous nucleoli are present in cells actively carrying out protein synthesis.
B. Nuclear pores allow bidirectional movement of molecules.
C. Cytoskeleton is a glycolipid structure for mechanical support, motility and maintenance of the shape of the cell.
D. Steroidal hormones are synthesized by Golgi complex.
- B and C
- C and D
- A and D
- A and B
(i) The myosin head pulls the actin filament towards the M-line.
(ii) The myosin head releases ADP and phosphate.
(iii) The myosin head hydrolyses ATP.
(iv) The myosin head binds actin.
- i, ii, iii, iv
- i, iii, ii, iv
- ii, iii, i, iv
- iii, iv, i, ii
I. ATP binding site
II. Actin binding site
III. Myosin binding site
IV. Troponin binding site
V. Calcium binding
- I and II
- I and III
- I, III, and V
- I, III and IV
- Ca binding sites on actin
- Ca binding sites on troponin
- actin binding site on myosin
- myosin binding site on actin
i. Contraction of muscle is an active process.
ii. Relaxation of muscle is an active process.
iii. Calcium is stored in sarcoplasmic reticulum.
- Both i and ii
- Both i and iii
- Only iii
- Only i
Reason: Calcium ions bind troponin causing the displacement of tropomyosin, allowing the myosin head to bind actin.
Select the appropriate option:
- Both assertion and reason are correct statements and reason is the correct explanation of the assertion
- Both assertion and reason are correct statements and reason is an incorrect explanation of the assertion
- Only assertion is correct
- Both assertion and reason are incorrect
What is treadmilling?
(i) A band
(ii) I band
(iii) Sarcomere
- i and ii
- ii and iii
- i and iii
- i, ii and iii
During contraction of muscles
actin filament slide
actin filament slide over myosin
myosin filament slide over actin
myosin filament slide over myosin.
How does a muscle shorten during its contraction and return to its original form during relaxation?
- troponin
- tropomyosin
- troponin-tropomyosin complex
- none of these
- Filament sliding occurs
- Filament sliding stops
- Muscle relaxes
- No change in muscle state
- H-zone
- M-zone
- I-zone
- Z-zone
- Actin
- Troponin
- Tropomyosin
- Myosin
According to the sliding filament mechanism of skeletal-muscle contraction, during contraction:
Both thick and thin filaments shorten.
The thick filaments stay the same size but the thin filaments shorten.
The sarcomeres shorten.
The thin filaments stay the same size but the thick filaments shorten.
- ATP
- phosphocreatine
- glycogen
- phosphocreatine kinase
- The myosin head pivots toward the middle of the sarcomere and pulls the attached actin filament with it.
- The actin head pivots toward the middle of the sarcomere and pulls the attached myosin filament with it.
- Ca++ ions are removed from the sarcoplasm
- Crossbridges rotate so that the myosin filaments fold in half
- loss of action potential reaching the muscle fibre
- loss of muscle contraction
- failure of dissociation of troponin from tropomyosin
- both b and c
I. ATP binding site
II. Actin binding site
III. Myosin binding site
IV. Troponin binding site
V. Calcium binding
- I and II
- I and III
- I, III and IV
- I, III, and V
- actin
- myosin
- collagen
- creatine
- Ca++ and K+
- Na+ and K+
- Na+ and Ca++
- Ca++ and Mg++ ions
(i) The myosin head pulls the actin filament towards the M-line.
(ii) The myosin head releases ADP and phosphate.
(iii) The myosin head hydrolyses ATP.
(iv) The myosin head binds actin.
- i, ii, iii, iv
- i, iii, ii, iv
- ii, iii, i, iv
- iii, iv, i, ii
- Ca binding sites on actin
- Ca binding sites on troponin
- actin binding site on myosin
- myosin binding site on actin
- I
- H
- A
- Z-line
- H and Z lines
I. ATP binding site
II. Actin binding site
III. Myosin binding site
IV. Troponin binding site
V. Calcium binding
- I and II
- I and III
- I, III and IV
- I, III, and V
What is the correct sequence of events in the cross bridge formation?
i. The power stroke
ii. Cross bridge formation
iii. Myosin head is activated by ATP
iv. Calcium released binds to the troponin unblocks the actin sites
v. Cross bridge detachment
vi. Reactivation of the myosin head
iv, iii, ii, i, v, vi.
i, v, ii, iii, iv, vi.
iii, iv, i, v, ii, vi.
ii, i, iv, iii, v, vi.
Column I | Column II |
A. Structural and functional -unit of a myofibril | (i) H-zone |
B. Protein of thin filament | (ii) Myosin |
C. Protein of thick filament | (iii) Sarcomere |
D. The central part of thick filament not overlapped by thin filament | (iv) Actin |
- A-(i), B-(ii), C, (iii), D-(iv)
- A-(i), B-(iii), C-(ii), D-(iv)
- A-(i), B-(iv), C-(iii), D-(ii)
- A-(iii), B-(iv), C-(ii), D-(i)
- To break the cross bridges as a cofactor in the hydrolysis of ATP
- To bind with troponin, changing its shape so that the actin filament is exposed
- To transmit the action potential across the neuromuscular junction
- To re-establish the polarization of the plasma membrane following an action potential