Literature DB >> 35157266

Nanobodies: From Serendipitous Discovery of Heavy Chain-Only Antibodies in Camelids to a Wide Range of Useful Applications.

Fangling Ji1, Jun Ren1, Cécile Vincke2,3, Lingyun Jia1, Serge Muyldermans4,5.   

Abstract

The presence of unique heavy chain-only antibodies (HCAbs) in camelids was discovered at Vrije Universiteit Brussel (VUB, Brussels, Belgium) at a time when many researchers were exploring the cloning and expression of smaller antigen-binding fragments (Fv and Fab) from hybridoma-derived antibodies. The potential importance of this discovery was anticipated, and efforts were immediately undertaken to understand the emergence and ontogeny of these HCAbs as well as to investigate the applications of the single-domain antigen-binding variable domains of HCAbs (nanobodies). Nanobodies were demonstrated to possess multiple biochemical and biophysical advantages over other antigen-binding antibody fragments and alternative scaffolds. Today, nanobodies have a significant and growing impact on research, biotechnology, and medicine.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Camels; Heavy chain antibodies; Llamas; Nanobodies; Single domain antibodies; VHHs

Mesh:

Substances:

Year:  2022        PMID: 35157266     DOI: 10.1007/978-1-0716-2075-5_1

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  60 in total

1.  Single-domain antibody fragments with high conformational stability.

Authors:  Mireille Dumoulin; Katja Conrath; Annemie Van Meirhaeghe; Filip Meersman; Karel Heremans; Leon G J Frenken; Serge Muyldermans; Lode Wyns; Andre Matagne
Journal:  Protein Sci       Date:  2002-03       Impact factor: 6.725

2.  Phage antibodies: filamentous phage displaying antibody variable domains.

Authors:  J McCafferty; A D Griffiths; G Winter; D J Chiswell
Journal:  Nature       Date:  1990-12-06       Impact factor: 49.962

3.  Selection and identification of single domain antibody fragments from camel heavy-chain antibodies.

Authors:  M Arbabi Ghahroudi; A Desmyter; L Wyns; R Hamers; S Muyldermans
Journal:  FEBS Lett       Date:  1997-09-15       Impact factor: 4.124

4.  Crystal structure of a camel single-domain VH antibody fragment in complex with lysozyme.

Authors:  A Desmyter; T R Transue; M A Ghahroudi; M H Thi; F Poortmans; R Hamers; S Muyldermans; L Wyns
Journal:  Nat Struct Biol       Date:  1996-09

Review 5.  Prokaryotic expression of antibodies.

Authors:  Mehdi Arbabi-Ghahroudi; Jamshid Tanha; Roger MacKenzie
Journal:  Cancer Metastasis Rev       Date:  2005-12       Impact factor: 9.264

6.  Improved production and function of llama heavy chain antibody fragments by molecular evolution.

Authors:  R H van der Linden; B de Geus; G J Frenken; H Peters; C T Verrips
Journal:  J Biotechnol       Date:  2000-07-14       Impact factor: 3.307

7.  Heavy-chain antibodies in Camelidae; a case of evolutionary innovation.

Authors:  Viet Khong Nguyen; Chen Su; Serge Muyldermans; Wessel van der Loo
Journal:  Immunogenetics       Date:  2002-02-26       Impact factor: 2.846

8.  Assembly of a functional immunoglobulin Fv fragment in Escherichia coli.

Authors:  A Skerra; A Plückthun
Journal:  Science       Date:  1988-05-20       Impact factor: 47.728

9.  Reshaping human antibodies for therapy.

Authors:  L Riechmann; M Clark; H Waldmann; G Winter
Journal:  Nature       Date:  1988-03-24       Impact factor: 49.962

10.  Naturally occurring antibodies devoid of light chains.

Authors:  C Hamers-Casterman; T Atarhouch; S Muyldermans; G Robinson; C Hamers; E B Songa; N Bendahman; R Hamers
Journal:  Nature       Date:  1993-06-03       Impact factor: 49.962

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