Enzyme intermediates captured 'on the fly' by mix-and-inject serial crystallography

Bibliographic Details
Title: Enzyme intermediates captured 'on the fly' by mix-and-inject serial crystallography
Authors: Jose L. Olmos, Suraj Pandey, Jose M. Martin-Garcia, George Calvey, Andrea Katz, Juraj Knoska, Christopher Kupitz, Mark S. Hunter, Mengning Liang, Dominik Oberthuer, Oleksandr Yefanov, Max Wiedorn, Michael Heyman, Mark Holl, Kanupriya Pande, Anton Barty, Mitchell D. Miller, Stephan Stern, Shatabdi Roy-Chowdhury, Jesse Coe, Nirupa Nagaratnam, James Zook, Jacob Verburgt, Tyler Norwood, Ishwor Poudyal, David Xu, Jason Koglin, Matthew H. Seaberg, Yun Zhao, Saša Bajt, Thomas Grant, Valerio Mariani, Garrett Nelson, Ganesh Subramanian, Euiyoung Bae, Raimund Fromme, Russell Fung, Peter Schwander, Matthias Frank, Thomas A. White, Uwe Weierstall, Nadia Zatsepin, John Spence, Petra Fromme, Henry N. Chapman, Lois Pollack, Lee Tremblay, Abbas Ourmazd, George N. Phillips, Marius Schmidt
Source: BMC Biology, Vol 16, Iss 1, Pp 1-15 (2018)
Publisher Information: BMC, 2018.
Publication Year: 2018
Collection: LCC:Biology (General)
Subject Terms: Biology (General), QH301-705.5
More Details: Abstract Background Ever since the first atomic structure of an enzyme was solved, the discovery of the mechanism and dynamics of reactions catalyzed by biomolecules has been the key goal for the understanding of the molecular processes that drive life on earth. Despite a large number of successful methods for trapping reaction intermediates, the direct observation of an ongoing reaction has been possible only in rare and exceptional cases. Results Here, we demonstrate a general method for capturing enzyme catalysis “in action” by mix-and-inject serial crystallography (MISC). Specifically, we follow the catalytic reaction of the Mycobacterium tuberculosis β-lactamase with the third-generation antibiotic ceftriaxone by time-resolved serial femtosecond crystallography. The results reveal, in near atomic detail, antibiotic cleavage and inactivation from 30 ms to 2 s. Conclusions MISC is a versatile and generally applicable method to investigate reactions of biological macromolecules, some of which are of immense biological significance and might be, in addition, important targets for structure-based drug design. With megahertz X-ray pulse rates expected at the Linac Coherent Light Source II and the European X-ray free-electron laser, multiple, finely spaced time delays can be collected rapidly, allowing a comprehensive description of biomolecular reactions in terms of structure and kinetics from the same set of X-ray data.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1741-7007
93693494
Relation: http://link.springer.com/article/10.1186/s12915-018-0524-5; https://doaj.org/toc/1741-7007
DOI: 10.1186/s12915-018-0524-5
Access URL: https://doaj.org/article/cc4fc7b9369349448afd757a6952a22b
Accession Number: edsdoj.4fc7b9369349448afd757a6952a22b
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:17417007
93693494
DOI:10.1186/s12915-018-0524-5
Published in:BMC Biology
Language:English