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Engineered PROTAC-CID Systems for Mammalian Inducible Gene Regulation.
Ma, Dacheng; Yuan, Qichen; Peng, Fei; Paredes, Victor; Zeng, Hongzhi; Osikpa, Emmanuel C; Yang, Qiaochu; Peddi, Advaith; Patel, Anika; Liu, Megan S; Sun, Zheng; Gao, Xue.
Afiliação
  • Ma D; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas77005, United States.
  • Yuan Q; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas77005, United States.
  • Peng F; Department of Medicine, Division of Diabetes, Endocrinology and Metabolism, Baylor College of Medicine, Houston, Texas77030, United States.
  • Paredes V; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas77005, United States.
  • Zeng H; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas77005, United States.
  • Osikpa EC; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas77005, United States.
  • Yang Q; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas77005, United States.
  • Peddi A; Department of Biosciences, Rice University, Houston, Texas77005, United States.
  • Patel A; Department of Computer Sciences, Rice University, Houston, Texas77005, United States.
  • Liu MS; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas77005, United States.
  • Sun Z; Department of Medicine, Division of Diabetes, Endocrinology and Metabolism, Baylor College of Medicine, Houston, Texas77030, United States.
  • Gao X; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas77030, United States.
J Am Chem Soc ; 145(3): 1593-1606, 2023 01 25.
Article em En | MEDLINE | ID: mdl-36626587
Gene regulation via chemically induced dimerization (CID) is useful for biomedical research. However, the number, type, versatility, and in vivo applications of CID tools remain limited. Here, we demonstrate the development of proteolysis-targeting chimera-based scalable CID (PROTAC-CID) platforms by systematically engineering the available PROTAC systems for inducible gene regulation and gene editing. Further, we show orthogonal PROTAC-CIDs that can fine-tune gene expression at gradient levels or multiplex biological signals with different logic gating operations. Coupling the PROTAC-CID platform with genetic circuits, we achieve digitally inducible expression of DNA recombinases, base- and prime-editors for transient genome manipulation. Finally, we package a compact PROTAC-CID system into adeno-associated viral vectors for inducible and reversible gene activation in vivo. This work provides a versatile molecular toolbox that expands the scope of chemically inducible gene regulation in human cells and mice.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Recombinases Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Recombinases Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article