Ultrafast myoglobin structural dynamics observed with an X-ray free-electron laser
Abstract
Light absorption can trigger biologically relevant protein conformational changes. The light induced structural rearrangement at the level of a photoexcited chromophore is known to occur in the femtosecond timescale and is expected to propagate through the protein as a quake-like intramolecular motion. Here we report direct experimental evidence of such ‘proteinquake’ observed in myoglobin through femtosecond X-ray solution scattering measurements performed at the Linac Coherent Light Source X-ray free-electron laser. An ultrafast increase of myoglobin radius of gyration occurs within 1 picosecond and is followed by a delayed protein expansion. As the system approaches equilibrium it undergoes damped oscillations with a ~3.6-picosecond time period. Our results unambiguously show how initially localized chemical changes can propagate at the level of the global protein conformation in the picosecond timescale.
- Authors:
-
- Univ. of Palermo (Italy). Dept. of Physics.
- Univ. of Grenoble Alpes and Institute of Structural Biology (France)
- SLAC National Accelerator Laboratory, Menlo Park, CA (Untied States)
- Inst. for Basic Science (IBS), Daejeon (Republic of Korea)
- Republic of Korea
- Univ. of Rennes (France). Dept. of Physics.
- Publication Date:
- Research Org.:
- SLAC National Accelerator Laboratory (SLAC), Menlo Park, CA (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC)
- OSTI Identifier:
- 1189945
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Nature Communications
- Additional Journal Information:
- Journal Volume: 6; Journal Issue: 3; Journal ID: ISSN 2041-1723
- Publisher:
- Nature Publishing Group
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES
Citation Formats
Levantino, Matteo, Schirò, Giorgio, Lemke, Henrik Till, Cottone, Grazia, Glownia, James Michael, Zhu, Diling, Chollet, Mathieu, Ihee, Hyotcherl, KAIST, Daejeon, Cupane, Antonio, and Cammarata, Marco. Ultrafast myoglobin structural dynamics observed with an X-ray free-electron laser. United States: N. p., 2015.
Web. doi:10.1038/ncomms7772.
Levantino, Matteo, Schirò, Giorgio, Lemke, Henrik Till, Cottone, Grazia, Glownia, James Michael, Zhu, Diling, Chollet, Mathieu, Ihee, Hyotcherl, KAIST, Daejeon, Cupane, Antonio, & Cammarata, Marco. Ultrafast myoglobin structural dynamics observed with an X-ray free-electron laser. United States. https://doi.org/10.1038/ncomms7772
Levantino, Matteo, Schirò, Giorgio, Lemke, Henrik Till, Cottone, Grazia, Glownia, James Michael, Zhu, Diling, Chollet, Mathieu, Ihee, Hyotcherl, KAIST, Daejeon, Cupane, Antonio, and Cammarata, Marco. Thu .
"Ultrafast myoglobin structural dynamics observed with an X-ray free-electron laser". United States. https://doi.org/10.1038/ncomms7772. https://www.osti.gov/servlets/purl/1189945.
@article{osti_1189945,
title = {Ultrafast myoglobin structural dynamics observed with an X-ray free-electron laser},
author = {Levantino, Matteo and Schirò, Giorgio and Lemke, Henrik Till and Cottone, Grazia and Glownia, James Michael and Zhu, Diling and Chollet, Mathieu and Ihee, Hyotcherl and KAIST, Daejeon and Cupane, Antonio and Cammarata, Marco},
abstractNote = {Light absorption can trigger biologically relevant protein conformational changes. The light induced structural rearrangement at the level of a photoexcited chromophore is known to occur in the femtosecond timescale and is expected to propagate through the protein as a quake-like intramolecular motion. Here we report direct experimental evidence of such ‘proteinquake’ observed in myoglobin through femtosecond X-ray solution scattering measurements performed at the Linac Coherent Light Source X-ray free-electron laser. An ultrafast increase of myoglobin radius of gyration occurs within 1 picosecond and is followed by a delayed protein expansion. As the system approaches equilibrium it undergoes damped oscillations with a ~3.6-picosecond time period. Our results unambiguously show how initially localized chemical changes can propagate at the level of the global protein conformation in the picosecond timescale.},
doi = {10.1038/ncomms7772},
journal = {Nature Communications},
number = 3,
volume = 6,
place = {United States},
year = {Thu Apr 02 00:00:00 EDT 2015},
month = {Thu Apr 02 00:00:00 EDT 2015}
}
Web of Science
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