| Literature DB >> 24510545 |
Toya Nath Baral1, Roger MacKenzie1,2, Mehdi Arbabi Ghahroudi1,2,3.
Abstract
Engineered monoclonal antibody fragments have gained market attention due to their versatility and tailor-made potential and are now considered to be an important part of future immunobiotherapeutics. Single-domain antibodies (sdAbs), also known as nanobodies, are derived from VHHs [variable domains (V) of heavy-chain-only antibodies (HCAb)] of camelid heavy-chain antibodies. These nature-made sdAbs are well suited for various applications due to their favorable characteristics such as small size, ease of genetic manipulation, high affinity and solubility, overall stability, resistance to harsh conditions (e.g., low pH, high temperature), and low immunogenicity. Most importantly, sdAbs have the feature of penetrating into cavities and recognizing hidden epitopes normally inaccessible to conventional antibodies, mainly due to their protruding CDR3/H3 loops. In this unit, we will present and discuss comprehensive and step-by-step protocols routinely practiced in our laboratory for isolating sdAbs from immunized llamas (or other members of the Camelidae family) against target antigens using phage-display technology. Expression, purification, and characterization of the isolated sdAbs will then be described, followed by presentation of several examples of applications of sdAbs previously characterized in our laboratory and elsewhere.Entities:
Keywords: VHH; antibody fragment libraries dimeric VHH; heavy-chain antibodies; multivalency; pentabodies; single-domain antibody
Mesh:
Substances:
Year: 2013 PMID: 24510545 DOI: 10.1002/0471142735.im0217s103
Source DB: PubMed Journal: Curr Protoc Immunol ISSN: 1934-3671