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1.
Prep Biochem Biotechnol ; 53(7): 728-752, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36534636

RESUMEN

The formation of inclusion bodies (IBs) during expression of recombinant therapeutic proteins using E. coli is a significant hurdle in producing high-quality, safe, and efficacious medicines. The improved understanding of the structure-function relationship of the IBs has resulted in the development of novel biotechnologies that have streamlined the isolation, solubilization, refolding, and purification of the active functional proteins from the bacterial IBs. Together, this overall effort promises to radically improve the scope of experimental biology of therapeutic protein production and expand new prospects in IBs usage. Notably, the IBs are increasingly used for applications in more pristine areas such as drug delivery and material sciences. In this review, we intend to provide a comprehensive picture of the bio-processing of bacterial IBs, including assessing critical gaps that still need to be addressed and potential solutions to overcome them. We expect this review to be a useful resource for those working in the area of protein refolding and therapeutic protein production.


Asunto(s)
Escherichia coli , Cuerpos de Inclusión , Proteínas Recombinantes , Escherichia coli/genética , Escherichia coli/metabolismo , Cuerpos de Inclusión/metabolismo , Proteínas Recombinantes/biosíntesis , Relación Estructura-Actividad
2.
Biochem Pharmacol ; 225: 116303, 2024 07.
Artículo en Inglés | MEDLINE | ID: mdl-38797272

RESUMEN

Biotherapeutics hold great promise for the treatment of several diseases and offer innovative possibilities for new treatments that target previously unaddressed medical needs. Despite successful transitions from preclinical to clinical stages and regulatory approval, there are instances where adverse reactions arise, resulting in product withdrawals. As a result, it is essential to conduct thorough evaluations of safety and effectiveness on an individual basis. This article explores current practices, challenges, and future approaches in conducting comprehensive preclinical assessments to ensure the safety and efficacy of biotherapeutics including monoclonal antibodies, toxin-conjugates, bispecific antibodies, single-chain antibodies, Fc-engineered antibodies, antibody mimetics, and siRNA-antibody/peptide conjugates.


Asunto(s)
Anticuerpos Monoclonales , Evaluación Preclínica de Medicamentos , Humanos , Anticuerpos Monoclonales/química , Anticuerpos Monoclonales/inmunología , Anticuerpos Monoclonales/uso terapéutico , Animales , Evaluación Preclínica de Medicamentos/métodos , Anticuerpos Biespecíficos/química , Anticuerpos Biespecíficos/inmunología , Inmunoconjugados/química
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