4.6 Review

Nanobodies as Probes for Protein Dynamics in Vitro and in Cells

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 291, Issue 8, Pages 3767-3775

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.R115.679811

Keywords

nuclear magnetic resonance (NMR); protein domain; protein dynamic; single-domain antibody (sdAb; nanobody); X-ray crystallography; nanobody; protein dynamics; protein structure; protein engineering

Funding

  1. Canadian Institutes of Health Research
  2. Saskatchewan Health Research Foundation
  3. National Institutes of Health [GM067166]

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Nanobodies are the recombinant antigen-recognizing domains of the minimalistic heavy chain-only antibodies produced by camels and llamas. Nanobodies can be easily generated, effectively optimized, and variously derivatized with standard molecular biology protocols. These properties have triggered the recent explosion in the nanobody use in basic and clinical research. This review focuses on the emerging use of nanobodies for understanding and monitoring protein dynamics on the scales ranging from isolated protein domains to live cells, from nanoseconds to hours. The small size and high solubility make nanobodies uniquely suited for studying protein dynamics by NMR. The ability to produce conformation-sensitive nanobodies in cells enables studies that link structural dynamics of a target protein to its cellular behavior. The link between in vitro and in-cell dynamics, afforded by nanobodies, brings the analysis of such important events as receptor signaling, membrane protein trafficking, and protein interactions to the next level of resolution.

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