A C1qTNF3 collagen domain fusion chaperones diverse secreted proteins and anti-Aβ scFvs: Applications for gene therapies

Bibliographic Details
Title: A C1qTNF3 collagen domain fusion chaperones diverse secreted proteins and anti-Aβ scFvs: Applications for gene therapies
Authors: Brenda D. Moore, Yong Ran, Marshall S. Goodwin, Kavitha Komatineni, Karen N. McFarland, Kristy Dillon, Caleb Charles, Danny Ryu, Xuefei Liu, Stefan Prokop, Benoit I. Giasson, Todd E. Golde, Yona Levites
Source: Molecular Therapy: Methods & Clinical Development, Vol 31, Iss , Pp 101146- (2023)
Publisher Information: Elsevier, 2023.
Publication Year: 2023
Collection: LCC:Genetics
LCC:Cytology
Subject Terms: collagen domain, C1qTNF3, scFv, amyloid-β, immunotherapy, adeno-associated viral vector, Genetics, QH426-470, Cytology, QH573-671
More Details: Enhancing production of protein cargoes delivered by gene therapies can improve efficacy by reducing the amount of vector or simply increasing transgene expression levels. We explored the utility of a 126-amino acid collagen domain (CD) derived from the C1qTNF3 protein as a fusion partner to chaperone secreted proteins, extracellular “decoy receptor” domains, and single-chain variable fragments (scFvs). Fusions to the CD domain result in multimerization and enhanced levels of secretion of numerous fusion proteins while maintaining functionality. Efficient creation of bifunctional proteins using the CD domain is also demonstrated. Recombinant adeno-associated viral vector delivery of the CD with a signal peptide resulted in high-level expression with minimal biological impact as assessed by whole-brain transcriptomics. As a proof-of-concept in vivo study, we evaluated three different anti-amyloid Aβ scFvs (anti-Aβ scFvs), alone or expressed as CD fusions, following viral delivery to neonatal CRND8 mice. The CD fusion increased half-life, expression levels, and improved efficacy for amyloid lowering of a weaker binding anti-Aβ scFv. These studies validate the potential utility of this small CD as a fusion partner for secretory cargoes delivered by gene therapy and demonstrate that it is feasible to use this CD fusion to create biotherapeutic molecules with enhanced avidity or bifunctionality.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2329-0501
Relation: http://www.sciencedirect.com/science/article/pii/S2329050123001857; https://doaj.org/toc/2329-0501
DOI: 10.1016/j.omtm.2023.101146
Access URL: https://doaj.org/article/6b461f0d9cea453d8528a9ec5184a9ec
Accession Number: edsdoj.6b461f0d9cea453d8528a9ec5184a9ec
Database: Directory of Open Access Journals
More Details
ISSN:23290501
DOI:10.1016/j.omtm.2023.101146
Published in:Molecular Therapy: Methods & Clinical Development
Language:English