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Time-resolved protein nanocrystallography using an X-ray free-electron laser

Cornell Affiliated Author(s)

Author

A. Aquila
M.S. Hunter
R.B. Doak
R.A. Kirian
P. Fromme
T.A. White
J. Andreasson
D. Arnlund
S. Bajt
T.R.M. Barends
M. Barthelmess
M.J. Bogan
C. Bostedt
H. Bottin
J.D. Bozek
C. Caleman
N. Coppola
J. Davidsson
D.P. DePonte
V. Elser
S.W. Epp
B. Erk
H. Fleckenstein
L. Foucar
M. Frank
R. Fromme
H. Graafsma
I. Grotjohann
L. Gumprecht
J. Hajdu
C.Y. Hampton
A. Hartmann
R. Hartmann
S.P. Hau-Riege
G. Hauser
H. Hirsemann
P. Holl
J.M. Holton
A. Hömke
L. Johansson
N. Kimmel
S. Kassemeyer
F. Krasniqi
K.-U. Kühnel
M. Liang
L. Lomb
E. Malmerberg
S. Marchesini
A.V. Martin
F.R.N.C. Maia
M. Messerschmidt
K. Nass
C. Reich
R. Neutze
D. Rolles
B. Rudek
A. Rudenko
I. Schlichting
C. Schmidt
K.E. Schmidt
J. Schulz
Marvin Seibert
R.L. Shoeman
R. Sierra
H. Soltau
D. Starodub
F. Stellato
S. Stern
L. Strüder
N. Timneanu
J. Ullrich
X. Wang
G.J. Williams
G. Weidenspointner
U. Weierstall
C. Wunderer
A. Barty
J.C.H. Spence
H.N. Chapman

Abstract

We demonstrate the use of an X-ray free electron laser synchronized with an optical pump laser to obtain X-ray diffraction snapshots from the photoactivated states of large membrane protein complexes in the form of nanocrystals flowing in a liquid jet. Light-induced changes of Photosystem I-Ferredoxin co-crystals were observed at time delays of 5 to 10 μs after excitation. The result correlates with the microsecond kinetics of electron transfer from Photosystem I to ferredoxin. The undocking process that follows the electron transfer leads to large rearrangements in the crystals that will terminally lead to the disintegration of the crystals. We describe the experimental setup and obtain the first timeresolved femtosecond serial X-ray crystallography results from an irreversible photo-chemical reaction at the Linac Coherent Light Source. This technique opens the door to time-resolved structural studies of reaction dynamics in biological systems. © 2012 Optical Society of America.

Date Published

Journal

Optics Express

Volume

20

Issue

3

Number of Pages

2706-2716,

URL

https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863010963&doi=10.1364%2fOE.20.002706&partnerID=40&md5=5d4aaf7faee75b0c18d1d1e44b368fb1

DOI

10.1364/OE.20.002706

Group (Lab)

Veit Elser Group

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