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General Strategy for Direct Cytosolic Protein Delivery via Protein-Nanoparticle Co-engineering.

ABSTRACT: Endosomal entrapment is a key hurdle for most intracellular protein-based therapeutic strategies. We report a general strategy for efficient delivery of proteins to the cytosol through co-engineering of proteins and nanoparticle vehicles. The proteins feature an oligo(glutamate) sequence (E-tag) that binds arginine-functionalized gold nanoparticles, generating hierarchical spherical nanoassemblies. These assemblies fuse with cell membranes, releasing the E-tagged protein directly into the cytosol. Five different proteins with diverse charges, sizes, and functions were effectively delivered into cells, demonstrating the generality of our method. Significantly, the engineered proteins retained activity after cytosolic delivery, as demonstrated through the delivery of active Cre recombinase, and granzyme A to kill cancer cells.

SUBMITTER: Mout R

PROVIDER: S-EPMC5766003 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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General Strategy for Direct Cytosolic Protein Delivery via Protein-Nanoparticle Co-engineering.

Mout Rubul R Ray Moumita M Tay Tristan T Sasaki Kanae K Yesilbag Tonga Gulen G Rotello Vincent M VM

ACS nano 20170615 6

Endosomal entrapment is a key hurdle for most intracellular protein-based therapeutic strategies. We report a general strategy for efficient delivery of proteins to the cytosol through co-engineering of proteins and nanoparticle vehicles. The proteins feature an oligo(glutamate) sequence (E-tag) that binds arginine-functionalized gold nanoparticles, generating hierarchical spherical nanoassemblies. These assemblies fuse with cell membranes, releasing the E-tagged protein directly into the cytoso ...[more]

PMID: 28614657

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