Serial femtosecond crystallography (SFX) using X-ray free-electron laser sources is an emerging method with considerable potential for time-resolved pump-probe experiments. Here we present a lipidic cubic phase SFX structure of the light-driven proton pump bacteriorhodopsin (bR) to 2.3 Å resolution and a method to investigate protein dynamics with modest sample requirement. Time-resolved SFX (TR-SFX) with a pump-probe delay of 1 ms yields difference Fourier maps compatible with the dark to M state transition of bR. Importantly, the method is very sample efficient and reduces sample consumption to about 1 mg per collected time point. Accumulation of M intermediate within the crystal lattice is confirmed by time-resolved visible absorption sp...
X-ray free-electron lasers (XFELs) have opened new opportunities for timeresolved X-ray crystallogra...
During my PhD studies at the ETH Zurich and the Paul Scherrer Institute I worked in the field of tim...
X-ray crystallography has provided the vast majority of three-dimensional macromolecular structures....
Serial femtosecond crystallography (SFX) using X-ray free-electron laser sources is an eme...
Lipidic cubic phases (LCPs) have emerged as successful matrixes for the crystallization of membrane ...
Lipidic cubic phases (LCPs) have emerged as successful matrixes for the crystallization of membrane ...
Structural information of the different conformational states of the two prototypical light-sensitiv...
Proteins that change their structure in response to light absorption regulate many functional proces...
Serial femtosecond crystallography (SFX) at X-ray free-electron lasers (XFELs) enables high-resoluti...
Rhodopsin is a membrane protein from the G protein-coupled receptor family. Together with its ligand...
With the advent of X-ray free-electron lasers (XFELs), new, high-throughput serial crystallography t...
Serial femtosecond crystallography using ultrashort pulses from x-ray free electron lasers (XFELs) e...
Serial Femtosecond X-ray nanocrystallography (SFX) is a recently developed technique for protein str...
Rhodopsins are a family of membrane proteins that are found in a wide range of organisms and provide...
Serial femtosecond crystallography (SFX) has opened a new era in crystallography by permitting nearl...
X-ray free-electron lasers (XFELs) have opened new opportunities for timeresolved X-ray crystallogra...
During my PhD studies at the ETH Zurich and the Paul Scherrer Institute I worked in the field of tim...
X-ray crystallography has provided the vast majority of three-dimensional macromolecular structures....
Serial femtosecond crystallography (SFX) using X-ray free-electron laser sources is an eme...
Lipidic cubic phases (LCPs) have emerged as successful matrixes for the crystallization of membrane ...
Lipidic cubic phases (LCPs) have emerged as successful matrixes for the crystallization of membrane ...
Structural information of the different conformational states of the two prototypical light-sensitiv...
Proteins that change their structure in response to light absorption regulate many functional proces...
Serial femtosecond crystallography (SFX) at X-ray free-electron lasers (XFELs) enables high-resoluti...
Rhodopsin is a membrane protein from the G protein-coupled receptor family. Together with its ligand...
With the advent of X-ray free-electron lasers (XFELs), new, high-throughput serial crystallography t...
Serial femtosecond crystallography using ultrashort pulses from x-ray free electron lasers (XFELs) e...
Serial Femtosecond X-ray nanocrystallography (SFX) is a recently developed technique for protein str...
Rhodopsins are a family of membrane proteins that are found in a wide range of organisms and provide...
Serial femtosecond crystallography (SFX) has opened a new era in crystallography by permitting nearl...
X-ray free-electron lasers (XFELs) have opened new opportunities for timeresolved X-ray crystallogra...
During my PhD studies at the ETH Zurich and the Paul Scherrer Institute I worked in the field of tim...
X-ray crystallography has provided the vast majority of three-dimensional macromolecular structures....