Part:BBa_K3123001:Design
CBD Nanobody Luciferase
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1977
Illegal BamHI site found at 1307
Illegal XhoI site found at 1929 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 290
Illegal NgoMIV site found at 1404
Illegal AgeI site found at 711
Illegal AgeI site found at 1825 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part is a variation of biobrick BBa_K3123000, but does not include the FKPA chaperone protein.
Source
This part came from a synthetic library of nanobodies. The library was created from trinucleotide mutagenesis (TRIM) on the nanobodies naturally found in camels. These nanobodies all share a common scaffold, and have variable regions that allow for a variety of binding. After an extensive screening process this nanobody was chosen because of its binding specificity to CBD. The luciferase coding sequence was identified from Oplophorus gracilirostris, a deep sea shrimp.
References
1. Shoukai Kang, Kristian Davidsen, Luis Gomez-Castillo, Huayi Jiang, Xiaonan Fu, Zengpeng Li, Yu Liang, Molly Jahn, Mahmoud Moussa, Frank DiMaio, and Liangcai Gu Journal of the American Chemical Society 2019 141 (28), 10948-10952 DOI: 10.1021/jacs.9b03522
2. Andrew S. Dixon, Marie K. Schwinn, Mary P. Hall, Kris Zimmerman, Paul Otto, Thomas H. Lubben, Braeden L. Butler, Brock F. Binkowski, Thomas Machleidt, Thomas A. Kirkland, Monika G. Wood, Christopher T. Eggers, Lance P. Encell, and Keith V. Wood ACS Chemical Biology 2016 11 (2), 400-408 DOI: 10.1021/acschembio.5b00753