A Multifunctional Peptide‐Conjugated AIEgen for Efficient and Sequential Targeted Gene Delivery into the Nucleus
Gene therapy has immense potential as a therapeutic approach to serious diseases. However, efficient delivery and real‐time tracking of gene therapeutic agents have not been solved well for successful gene‐based therapeutics. Herein we present a versatile gene‐delivery strategy for efficient and vis...
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Veröffentlicht in: | Angewandte Chemie 2019-04, Vol.131 (15), p.5103-5107 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Gene therapy has immense potential as a therapeutic approach to serious diseases. However, efficient delivery and real‐time tracking of gene therapeutic agents have not been solved well for successful gene‐based therapeutics. Herein we present a versatile gene‐delivery strategy for efficient and visualized delivery of therapeutic genes into the targeted nucleus. We developed an integrin‐targeted, cell‐permeable, and nucleocytoplasmic trafficking peptide‐conjugated AIEgen named TDNCP for the efficient and sequential targeted delivery of an antisense single‐stranded DNA oligonucleotide (ASO) and tracking of the delivery process into the nucleus. As compared with TDNCP/siRNA‐NPs (siRNA functions mainly in the cytoplasm), TDNCP/ASO‐NPs (ASO functions mainly in the nucleus) exhibited a better interference effect, which further indicates that TDNCP is a nucleus‐targeting vector. Moreover, TDNCP/ASO‐NPs showed a favorable tumor‐suppressive effect in vivo.
Verfolgen der Lieferung: Das Konjugat TNCP transportiert Gentherapeutika in den Kern von Krebszellen und ermöglicht deren Echtzeitverfolgung. TNCP besteht aus vier Segmenten: einem Target‐Peptid (Ligand für den Integrin‐αvβ3‐Rezeptor), einem Kernlokalisierungssignal, einem zelldurchdringenden Peptid und PyTPE, einem Molekül mit AIE‐Eigenschaften. Nanopartikel, die mit einem Antisense‐Oligonukleotid (ASO) gebildet wurden, zielen auf Krebszellen und unterdrücken das Tumorwachstum. |
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ISSN: | 0044-8249 1521-3757 |
DOI: | 10.1002/ange.201901527 |