Nanobodies – A potential
Therapeutics
Ms.
Megha Chaturvedi.
Assistant
professor (Faculty of science)
Department
of Biotechnology
Kalinga
University, Raipur, Chhattisgarh
Nanobodies have been widely used in the field of research,
diagnosis, and therapy ever since their discovery. These Camelid heavy-chain
antibody-derived antigen-binding fragments have remarkable characteristics in
terms of (small) size, stability, solubility, and specificity, enabling
cost-effective synthesis and occasionally outperforming monoclonal antibodies.
In general, monoclonal antibodies are well tolerated, as they are substantial
proteins (typically 150-200,000 Daltons in size). In contrast to other monoclonal antibodies,
nanobodies are made up of a single heavy-chain variable domain that can bind
its antigen just as strongly as a regular antibody, produced from a camelid IgG
variation. A long-lasting, ready-to-use solution for nanobodies is conceivable.
Moreover, nanobodies are relatively simple to make in bacterial, yeast, or mammalian
cells, allowing for high-volume manufacture at affordable prices. Furthermore,
nanobodies are easily used as building blocks for multi-domain constructions,
and recombinant synthesis in microorganisms is particularly cost-effective (Muyldermans S. 2013). As ligand-receptor inhibitors and
carriers of medications or medication-loaded nanoparticles for tumor delivery,
nanobodies have significant therapeutic potential. Preclinical cancer cell line
models are used in a variety of experimental contexts, such as cell adhesion,
proliferation, migration, angiogenesis-like features, or disruption of certain
signaling pathways, to forecast the therapeutic efficacy of nanobody
therapeutics. Their small size is helpful for deeper and homogenous tumor
penetration but detrimental for in vivo half-life (few hours). In order to
enable binding to serum albumin (66 kDa), nanobodies are frequently coupled to
an anti-albumin nanobody. However, more
in vivo and clinical research is eagerly anticipated to improve in the future.
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