International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 281, P. 136403 - 136403
Published: Oct. 9, 2024
Language: Английский
International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 281, P. 136403 - 136403
Published: Oct. 9, 2024
Language: Английский
Biomedicines, Journal Year: 2025, Volume and Issue: 13(3), P. 637 - 637
Published: March 5, 2025
Background: Monoclonal antibodies (mAbs) are potent treatment options for infectious diseases. The rapid isolation and in vivo validation of therapeutic mAb candidates, including cocktails, essential to combat novel or rapidly mutating pathogens. selection production candidates sufficient amount quality preclinical studies a major limiting step the development pipeline. Methods: Here, we developed method facilitate screening mAbs mouse models. Four conventional were transformed into single-chain variable fragments fused fragment crystallizable (Fc) region human IgG1 (scFv-IgG). These scFv-IgG expressed individually as cocktail vitro mice following transfection hydrodynamic delivery corresponding plasmids. Results: This induced high expression all provided protection two murine infection Conclusions: study highlights benefits this approach rapid, low-cost candidates.
Language: Английский
Citations
0mAbs, Journal Year: 2025, Volume and Issue: 17(1)
Published: April 9, 2025
Viral infections remain a significant global health threat, with emerging and reemerging viruses causing epidemics pandemics. Despite advancements in antiviral therapies, the development of effective treatments is often hindered by challenges, such as viral resistance emergence new strains. In this context, novel therapeutic modalities essential to combat notorious viruses. While traditional monoclonal antibodies are widely used for treatment several diseases, nanobodies derived from heavy chain-only have emerged promising "nanoscale warriors" against infections. Nanobodies possess unique structural properties that enhance their ability recognize diverse epitopes. Their small size also imparts properties, improved bioavailability, solubility, stability, proteolytic resistance, making them an ideal class therapeutics review, we discuss role antivirals various Techniques developing nanobodies, delivery strategies covered, challenges opportunities associated use therapies discussed. We offer insights into future nanobody-based research support managing
Language: Английский
Citations
0ACS Omega, Journal Year: 2025, Volume and Issue: unknown
Published: April 21, 2025
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a virus of the coronaviridae family. The enters cell through binding to corresponding receptor angiotensin-converting enzyme (ACE2) on host membrane with spike protein (S protein) its envelope; thus, we can design inhibitors that bind S block entry into cells. Aptamers are single stranded DNA or RNA molecules form specific three-dimensional structures and their target high affinity specificity thus promising candidates for inhibitors. This paper reviews replication cycle mechanisms SARS-CoV-2 as well preparation principle characteristics aptamers, features discussion advantages using aptamers prevent from infecting cells, finally summarizes research progress in protein-blocking aptamers.
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 281, P. 136403 - 136403
Published: Oct. 9, 2024
Language: Английский
Citations
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