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Engineered red blood cells as carriers for systemic delivery of a wide array of functional probes.


ABSTRACT: We developed modified RBCs to serve as carriers for systemic delivery of a wide array of payloads. These RBCs contain modified proteins on their plasma membrane, which can be labeled in a sortase-catalyzed reaction under native conditions without inflicting damage to the target membrane or cell. Sortase accommodates a wide range of natural and synthetic payloads that allow modification of RBCs with substituents that cannot be encoded genetically. As proof of principle, we demonstrate site-specific conjugation of biotin to in vitro-differentiated mouse erythroblasts as well as to mature mouse RBCs. Thus modified, RBCs remain in the bloodstream for up to 28 d. A single domain antibody attached enzymatically to RBCs enables them to bind specifically to target cells that express the antibody target. We extend these experiments to human RBCs and demonstrate efficient sortase-mediated labeling of in vitro-differentiated human reticulocytes.

SUBMITTER: Shi J 

PROVIDER: S-EPMC4104923 | biostudies-literature | 2014 Jul

REPOSITORIES: biostudies-literature

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Engineered red blood cells as carriers for systemic delivery of a wide array of functional probes.

Shi Jiahai J   Kundrat Lenka L   Pishesha Novalia N   Bilate Angelina A   Theile Chris C   Maruyama Takeshi T   Dougan Stephanie K SK   Ploegh Hidde L HL   Lodish Harvey F HF  

Proceedings of the National Academy of Sciences of the United States of America 20140630 28


We developed modified RBCs to serve as carriers for systemic delivery of a wide array of payloads. These RBCs contain modified proteins on their plasma membrane, which can be labeled in a sortase-catalyzed reaction under native conditions without inflicting damage to the target membrane or cell. Sortase accommodates a wide range of natural and synthetic payloads that allow modification of RBCs with substituents that cannot be encoded genetically. As proof of principle, we demonstrate site-specif  ...[more]

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