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The cellular mRNA uptake and translation machinery is a complex, multi-component system responsible for the internalization of exogenous mRNA and its subsequent conversion into functional polypeptides. This process typically involves the endocytosis of mRNA—often encapsulated in lipid nanoparticles (LNPs)—followed by endosomal escape into the cytosol (Sahin et al., 2014, Nature Reviews Drug Discovery). Once in the cytoplasm, the mRNA interacts with the eukaryotic initiation factor 4F (eIF4F) complex and the 40S ribosomal subunit to initiate translation (Jackson et al., 2010, Nature Reviews Molecular Cell Biology). The machinery then facilitates elongation and termination to produce the encoded protein. While not a single molecular target, this system is the fundamental platform for mRNA vaccines and gene therapies, which leverage host ribosomes to produce therapeutic antigens or proteins. Additionally, specific components of this machinery, such as the ribosome or initiation factors, are targeted by small molecules to inhibit protein synthesis in cancer or infectious diseases (Bhat et al., 2015, Nature Reviews Drug Discovery).
Exogenous mRNA is internalized via endocytosis, released into the cytoplasm through endosomal escape, and subsequently translated by host ribosomes and initiation factors into functional proteins.
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