Answer:
When a muscle cell contracts, the myosin heads each produce a single power stroke.
Explanation:
In rest, attraction strengths between myosin and actin filaments are inhibited by the tropomyosin. When the muscle fiber membrane depolarizes, the action potential caused by this depolarization enters the t-tubules depolarizing the inner portion of the muscle fiber. This activates calcium channels in the T tubules membrane and releases calcium into the sarcolemma. At this point, <em>tropomyosin is obstructing binding sites for myosin on the thin filament</em>. When calcium binds to the troponin C, the troponin T alters the tropomyosin by moving it and then unblocks the binding sites. Myosin heads bind to the uncovered actin-binding sites forming cross-bridges, and while doing it ATP is transformed into ADP and inorganic phosphate which is liberated. Myofilaments slide impulsed by chemical energy collected in myosin heads, <u>producing a power stroke</u>. The power stroke initiates when the myosin cross-bridge binds to actin. As they slide, ADP molecules are released. A new ATP links to myosin heads and breaks the bindings to the actin filament. Then ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, which starts a new binding cycle to actin. Z-bands are then pulled toward each other, thus shortening the sarcomere and the I-band, and producing muscle fiber contraction.
They would constrict the diameter of blood vessels. Plaque and tobacco can block your arteries, inhibiting from doing their job.
Answer:
The correct answers are option A. "tethering proteins to the cell cortex", B. "using barriers such as tight junctions", C. "tethering proteins to the extracellular matrix", D. "forming a covalent linkage with membrane lipids", E. "tethering proteins to the surface of another cell"
Explanation:
According to the fluid-mosaic model, the components of cell membranes are in constant movement forming a barrier to avoid unwanted exterior component internalization and to avoid the loss of precious internal components. This constant movement could cause that proteins move across the plasma membrane. But, this is avoided by several mechanisms including:
A. Tethering proteins to the cell cortex. The cell cortex is a rigid structure made of actin and actomyosin. Proteins found in the plasma membrane are tethered to this structure to restrict their movement.
B. Using barriers such as tight junctions. Tight junctions are barriers found in epithelia made of claudin and occludin proteins. These barriers are impenetrable, which avoid the movement of proteins in the cell membrane.
C. Tethering proteins to the extracellular matrix. The extracellular matrix is made of several proteins and macromolecules that provide a structural and biochemical support to cells that are nearby. Proteins could be tethered to this rigid structure as well.
D. Forming a covalent linkage with membrane lipids. The proteins in the cell membrane that form a covalent linkage with membrane lipids are known as lipid-anchored proteins, or lipid-linked proteins.
E. Tethering proteins to the surface of another cell. When cell-cell communication take place it is possible that proteins in the cell membrane got tethered to the surface of the other cell.
<span>A scientific law describes repeated observations under a given set of conditions. These laws are not too specific, and they imply a casual relationship. These laws do not explain why something occurs, they merely state that something will occur if the given conditions are met. Therefore, the formation of a scientific law is a result of repeated observations. An example is Newton's first law of motion, which gives certain conditions for an object, such as no force acting on it, and then describes what the object will do in that situation, that is, remain in motion or remain stationary.</span>
If you conduct experiments and get consistent results and then change variables and again get consisnet results.
