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- W2040078811 endingPage "830" @default.
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- W2040078811 abstract "Proteins represent an expanding class of therapeutics, but their actions are limited primarily to extracellular targets because most peptidic molecules fail to enter cells. Here we identified two small proteins, miniature protein 5.3 and zinc finger module ZF5.3, that enter cells to reach the cytosol through rapid internalization and escape from Rab5+ endosomes. The trafficking pathway mapped for these molecules differs from that of Tat and Arg8, which require transport beyond Rab5+ endosomes to gain cytosolic access. Our results suggest that the ability of 5.3 and ZF5.3 to escape from early endosomes is a unique feature and imply the existence of distinct signals, encodable within short sequences, that favor early versus late endosomal release. Identifying these signals and understanding their mechanistic basis will illustrate how cells control the movement of endocytic cargo and may allow researchers to engineer molecules to follow a desired delivery pathway for rapid cytosolic access." @default.
- W2040078811 created "2016-06-24" @default.
- W2040078811 creator A5009748504 @default.
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- W2040078811 creator A5033763479 @default.
- W2040078811 creator A5067830024 @default.
- W2040078811 creator A5069765122 @default.
- W2040078811 date "2012-07-01" @default.
- W2040078811 modified "2023-09-27" @default.
- W2040078811 title "Arginine Topology Controls Escape of Minimally Cationic Proteins from Early Endosomes to the Cytoplasm" @default.
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- W2040078811 doi "https://doi.org/10.1016/j.chembiol.2012.05.022" @default.
- W2040078811 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3488872" @default.
- W2040078811 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22840770" @default.
- W2040078811 hasPublicationYear "2012" @default.
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