TY - JOUR
T1 - Nanobodies as probes for protein dynamics in vitro and in cells
AU - Dmitriev, Oleg Y.
AU - Lutsenko, Svetlana
AU - Muyldermans, Serge
N1 - Funding Information:
This work was supported by the Canadian Institutes of Health Research and Saskatchewan Health Research Foundation grants (to O. Y. D.) and by National Institutes of Health Grant GM067166 (to S. L). This is the second article in the Thematic Minireview series "Modern Technologies for In-cell Biochemistry." The authors declare that they have no conflicts of interest with the contents of this article. The content is solely the responsibility of the author and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.
PY - 2016/2/19
Y1 - 2016/2/19
N2 - 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 nano-bodies 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.
AB - 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 nano-bodies 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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U2 - 10.1074/jbc.R115.679811
DO - 10.1074/jbc.R115.679811
M3 - Review article
C2 - 26677230
AN - SCOPUS:85016923945
SN - 0021-9258
VL - 291
SP - 3767
EP - 3775
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 8
ER -