Therapeutic Fusion Proteins.


Journal

The AAPS journal
ISSN: 1550-7416
Titre abrégé: AAPS J
Pays: United States
ID NLM: 101223209

Informations de publication

Date de publication:
30 11 2023
Historique:
received: 17 08 2023
accepted: 08 11 2023
medline: 4 12 2023
pubmed: 1 12 2023
entrez: 30 11 2023
Statut: epublish

Résumé

Therapeutic fusion proteins are a class of hybrid constructs that combine distinct biomolecules into a single platform with the additive effects of the components. The ability to fuse two unrelated proteins provides a means to localize mechanisms to better treat a range of diseases. Fusion proteins can be designed to impart diverse functions, including increasing half-life, providing targeting, and enabling sustained signaling. Of these, half-life extenders, which are fused to a therapeutic protein to increase exposure, are the most established group of fusion proteins, with many clinical successes. Rapid advances in antibody and antibody-derivative technology have enabled the fusion of targeting domains with therapeutic proteins. An emerging group of therapeutic fusion proteins has two separate active functions. Although most research for therapeutic fusion proteins focuses on cancer, prior successes provide a foundation for studies into other diseases as well. The exponential emergence of biopharmaceuticals gives precedence for increased research into therapeutic fusion proteins for a multitude of diseases.

Identifiants

pubmed: 38036919
doi: 10.1208/s12248-023-00873-8
pii: 10.1208/s12248-023-00873-8
doi:

Substances chimiques

Proteins 0
Antibodies 0
Recombinant Fusion Proteins 0

Types de publication

Journal Article Review Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

3

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM134069
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA256460
Pays : United States

Informations de copyright

© 2023. The Author(s), under exclusive licence to American Association of Pharmaceutical Scientists.

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Auteurs

Morgan C Marsh (MC)

Department of Molecular Pharmaceutics, University of Utah, 30 South 2000 East, Room 301, Salt Lake City, Utah, 84112, USA.

Shawn C Owen (SC)

Department of Molecular Pharmaceutics, University of Utah, 30 South 2000 East, Room 301, Salt Lake City, Utah, 84112, USA. shawn.owen@hsc.utah.edu.
Department of Medicinal Chemistry, University of Utah, Salt Lake City, Utah, 84112, USA. shawn.owen@hsc.utah.edu.
Department of Biomedical Engineering, University of Utah, Salt Lake City, Utah, 84112, USA. shawn.owen@hsc.utah.edu.

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