We present a baculovirus-based protein engineering method that enables site-specific introduction of unique functionalities in a eukaryotic protein complex recombinantly produced in insect cells. We demonstrate the versatility of this efficient and robust protein production platform, ‘MultiBacTATAG’, (i) for the fluorescent labeling of target proteins and biologics using click chemistries, (ii) for glycoengineering of antibodies, and (iii) for structure–function studies of novel eukaryotic complexes using single-molecule Förster resonance energy transfer as well as site-specific crosslinking strategies.
Genetic code expansion for multiprotein complex engineering / C. Koehler, P.F. Sauter, M. Wawryszyn, G. Estrada Girona, K. Gupta. J.J.M. Landry, M. Hsi-Yang Fritz, K. Radic, J.E. Hoffmann, Z.A. Chen, J. Zou, P. Siong Tanv, B. Galik, S. Junttila, P. Stolt-Bergner, G. Pruneri, G. Attila, C. Schultz, M. Bosse Biskup, H. Besir, V. Benes, J. Rappsilber, M. Jechlinger, J.O. Korbel, I. Berger, S. Braese, E.A Lemke. - In: NATURE METHODS. - ISSN 1548-7091. - 13:12(2016 Dec), pp. 997-1000.
Genetic code expansion for multiprotein complex engineering
G. Pruneri;
2016
Abstract
We present a baculovirus-based protein engineering method that enables site-specific introduction of unique functionalities in a eukaryotic protein complex recombinantly produced in insect cells. We demonstrate the versatility of this efficient and robust protein production platform, ‘MultiBacTATAG’, (i) for the fluorescent labeling of target proteins and biologics using click chemistries, (ii) for glycoengineering of antibodies, and (iii) for structure–function studies of novel eukaryotic complexes using single-molecule Förster resonance energy transfer as well as site-specific crosslinking strategies.| File | Dimensione | Formato | |
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