Explanation:
First during protein synthesis, transcription occurs in the nucleus, followed by translation within ribosomes. Then, newly synthesized proteins enter endoplasmic reticulum where they undergo folding and modification. Next, within the golgi body, the proteins are tagged; after,they are finally parceled into lysosomes. Finally, they can be exported out of the cell to fulfill various functions.
Further Explanation:
The endoplasmic reticulum is a membrane system within the cytoplasm that extends from the outer nuclear membrane. Apart from increasing the surface area within the cell, this continuous system also carries out protein folding, synthesis and transport. In the endoplasmic reticulum or ER, some sections called the smooth ER, do not contain ribosomes, and may contain lipids, enzymes, and other proteins. Other sections bound to ribosomes, are called the rough Er. As a protein destined for the endomembrane system is being synthesized by a ribosome, the first amino acids in the growing polypeptide chain act as a signal sequence. That signal sequence ensures that the ribosome binds to the outer membrane of the ER and that the protein enters the ER lumen. The proteins undergo major modifications and are packed into vesicles.
Golgi bodies are flat, disk-like membranous regions. Proteins traverse the organelle by first having their vesicles bind to the cis face or receiving end. Like a post office, the golgi complex, or golgi body recognizes specific signal sequences, targets and further modifies and packages these compounds into lysosomes for delivery to their final destination. Proteins here undergo peptide processing and glycosylation
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Answer:
When an action potential reaches the end of an axon, the nervous terminal or the varicosities release neurotransmitters. These bind to receptors on the postsynaptic neuron. Eventually, the neurotransmitters are removed from the synapse. Some are reabsorbed by the presynaptic neuron or sending neuron, a process called reuptake, and some are broken down, in a process called enzymatic degradation.
Explanation:
Neurotransmitter liberation occurs from the nervous terminal or varicosities, in the neuronal axon. There are vesicles in the sending neuron that have neurotransmitters in their interior. When an <em>action potential reaches the nervous terminal</em> or the varicosities, it occurs a notable increase in the <em>neurotransmitter liberation</em> by exocytose. This is possible because calcium channels open letting the ion in the cell through the membrane, and letting the neurotransmitter out to the synaptic space. The molecule binds to its receptor in the postsynaptic neuron. This receptor is a <em>protein structure that triggers an answer</em>. As long as the signal molecule is in the synaptic space, it keeps linking to its receptor and causing a postsynaptic answer. <em>To stop this process</em>, the <em>neurotransmitter must be taken out from the synaptic space.</em> There are two mechanisms by which the neurotransmitter can be eliminated:
Enzymatic degradation/deactivation: In the synaptic space, there are <em>specific enzymes that can inactivate the neurotransmitter </em><em>by breaking it down or degrading it</em><em>.</em> In this case, the new molecule won’t be able to bind to the neurotransmitter receptor.
Reuptake: There are receptors located in the presynaptic membrane that can capture de molecule to store it back in new vesicles, for posterior use. These <em>transporters are active transport proteins</em> that easily recognize the neurotransmitter.