4.6 Review

Exploring cellular biochemistry with nanobodies

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 295, Issue 45, Pages 15307-15327

Publisher

ELSEVIER
DOI: 10.1074/jbc.REV120.012960

Keywords

single-domain antibody (SdAb); protein chemistry; antibody engineering; cell signaling; synthetic biology

Funding

  1. National Institutes of Health [1DP1AI150593, R01AI087879, R01-GM077537, R01-AR065484]
  2. Cancer Research Institute Irvington Postdoctoral Fellowship
  3. Swiss National Science Foundation (SNSF) [P400P2_183857]
  4. Swiss National Science Foundation (SNF) [P400P2_183857] Funding Source: Swiss National Science Foundation (SNF)

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Reagents that bind tightly and specifically to biomolecules of interest remain essential in the exploration of biology and in their ultimate application to medicine. Besides ligands for receptors of known specificity, agents commonly used for this purpose are monoclonal antibodies derived from mice, rabbits, and other animals. However, such antibodies can be expensive to produce, challenging to engineer, and are not necessarily stable in the context of the cellular cytoplasm, a reducing environment. Heavy chain-only antibodies, discovered in camelids, have been truncated to yield single-domain antibody fragments (VHHs or nanobodies) that overcome many of these shortcomings. Whereas they are known as crystallization chaperones for membrane proteins or as simple alternatives to conventional antibodies, nanobodies have been applied in settings where the use of standard antibodies or their derivatives would be impractical or impossible. We review recent examples in which the unique properties of nanobodies have been combined with complementary methods, such as chemical functionalization, to provide tools with unique and useful properties.

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