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Required to catalyze the GDP-GTP swap (dissociate GDP and eIF2)

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Final answer:

This college-level biology question relates to the molecular biology process of protein synthesis, specifically the role of the GDP-GTP swap catalyzed by eIF2B in the translational initiation phase. GTP-bound eIF2 forms a ternary complex necessary for scanning mRNA, and the subsequent GTP hydrolysis and GDP-to-GTP exchange on eIF2 is regulated by factors like hemin and HCR kinase. Disruption of GTP hydrolysis on eIF2 would stall translation initiation.

Step-by-step explanation:

The subject of this question is Biology, specifically within the area of molecular biology related to protein synthesis and the role of GTP/GDP in the initiation of translation. During the initiation of protein synthesis, GTP-bound eukaryotic initiation factor 2 (GTP-eIF2) binds methionine-charged initiator tRNA, forming a ternary complex (TC) that can associate with the scanning 40S ribosomal subunit. Upon locating the start codon of an mRNA, a complex series of molecular interactions result in the hydrolysis of GTP to GDP, which remains bound to eIF2. For new rounds of translation initiation, it is crucial that GDP is replaced by GTP on eIF2, a process catalyzed by eIF2B, an important regeneration factor.

To answer the question more directly, in cases of hemoglobin production, hemin regulates the initiation of globin mRNA translation. When hemin is in excess, it binds to HCR kinase, leaving GDP-eIF2 active and enabling the GTP/GDP swap to occur. In contrast, when heme and globin levels are balanced, hemin dissociates from HCR kinase, which then becomes active and phosphorylates eIF2B, rendering it unable to assist in the GDP-to-GTP exchange on eIF2, therefore slowing down globin translation.

Answering the hypothetical scenario mentioned, if eIF2's ability to hydrolyze GTP is lost due to a mutation, this would mean that GTP could not be converted back to GDP, ultimately stalling the translation process because regenerated GTP-eIF2 would not be available for initiating new rounds of synthesis. This would severely disrupt protein synthesis, as the recycling of GDP to GTP is a crucial step in translation initiation.

User Vahidg
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