Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Heike Soltau is active.

Publication


Featured researches published by Heike Soltau.


Nature | 2011

Femtosecond x-ray protein nanocrystallography

Henry N. Chapman; Petra Fromme; Anton Barty; Thomas A. White; Richard A. Kirian; Andrew Aquila; Mark S. Hunter; Joachim Schulz; Daniel P. DePonte; Uwe Weierstall; R. Bruce Doak; Filipe R. N. C. Maia; Andrew V. Martin; Ilme Schlichting; Lukas Lomb; Nicola Coppola; Robert L. Shoeman; Sascha W. Epp; Robert Hartmann; Daniel Rolles; A. Rudenko; Lutz Foucar; Nils Kimmel; Georg Weidenspointner; Peter Holl; Mengning Liang; Miriam Barthelmess; Carl Caleman; Sébastien Boutet; Michael J. Bogan

X-ray crystallography provides the vast majority of macromolecular structures, but the success of the method relies on growing crystals of sufficient size. In conventional measurements, the necessary increase in X-ray dose to record data from crystals that are too small leads to extensive damage before a diffraction signal can be recorded. It is particularly challenging to obtain large, well-diffracting crystals of membrane proteins, for which fewer than 300 unique structures have been determined despite their importance in all living cells. Here we present a method for structure determination where single-crystal X-ray diffraction ‘snapshots’ are collected from a fully hydrated stream of nanocrystals using femtosecond pulses from a hard-X-ray free-electron laser, the Linac Coherent Light Source. We prove this concept with nanocrystals of photosystem I, one of the largest membrane protein complexes. More than 3,000,000 diffraction patterns were collected in this study, and a three-dimensional data set was assembled from individual photosystem I nanocrystals (∼200 nm to 2 μm in size). We mitigate the problem of radiation damage in crystallography by using pulses briefer than the timescale of most damage processes. This offers a new approach to structure determination of macromolecules that do not yield crystals of sufficient size for studies using conventional radiation sources or are particularly sensitive to radiation damage.


Nature | 2011

Single mimivirus particles intercepted and imaged with an X-ray laser

M. Marvin Seibert; Tomas Ekeberg; Filipe R. N. C. Maia; Martin Svenda; Jakob Andreasson; O Jonsson; Duško Odić; Bianca Iwan; Andrea Rocker; Daniel Westphal; Max F. Hantke; Daniel P. DePonte; Anton Barty; Joachim Schulz; Lars Gumprecht; Nicola Coppola; Andrew Aquila; Mengning Liang; Thomas A. White; Andrew V. Martin; Carl Caleman; Stephan Stern; Chantal Abergel; Virginie Seltzer; Jean-Michel Claverie; Christoph Bostedt; John D. Bozek; Sébastien Boutet; A. Miahnahri; Marc Messerschmidt

X-ray lasers offer new capabilities in understanding the structure of biological systems, complex materials and matter under extreme conditions. Very short and extremely bright, coherent X-ray pulses can be used to outrun key damage processes and obtain a single diffraction pattern from a large macromolecule, a virus or a cell before the sample explodes and turns into plasma. The continuous diffraction pattern of non-crystalline objects permits oversampling and direct phase retrieval. Here we show that high-quality diffraction data can be obtained with a single X-ray pulse from a non-crystalline biological sample, a single mimivirus particle, which was injected into the pulsed beam of a hard-X-ray free-electron laser, the Linac Coherent Light Source. Calculations indicate that the energy deposited into the virus by the pulse heated the particle to over 100,000 K after the pulse had left the sample. The reconstructed exit wavefront (image) yielded 32-nm full-period resolution in a single exposure and showed no measurable damage. The reconstruction indicates inhomogeneous arrangement of dense material inside the virion. We expect that significantly higher resolutions will be achieved in such experiments with shorter and brighter photon pulses focused to a smaller area. The resolution in such experiments can be further extended for samples available in multiple identical copies.


Nuclear Instruments & Methods in Physics Research Section A-accelerators Spectrometers Detectors and Associated Equipment | 1996

Silicon drift detectors for high resolution room temperature X-ray spectroscopy

Peter Lechner; Stefan Eckbauer; Robert Hartmann; Susanne Krisch; D. Hauff; R. Richter; Heike Soltau; L. Strüder; C. Fiorini; E. Gatti; A. Longoni; M. Sampietro

New cylindrical silicon drift detectors have been designed, fabricated and tested. They comprise an integrated on-chip amplifier system with continuous reset, on-chip voltage divider, electron accumulation layer stabilizer, large area, homogeneous radiation entrance window and a drain for surface generated leakage current. The test of the 3.5 mm2 large individual devices, which have also been grouped together to form a sensitive area up to 21 mm2 have shown the following spectroscopic results: at room temperature (300 K) the devices have shown a full width at half maximum at the MnKα line of a radioactive 55 Fe source of 225 eV with shaping times of 250 to 500 ns. At −20°C the resolution improves to 152 eV at 2 μs Gaussian shaping. At temperatures below 200 K the energy resolution is below 140 eV. With the implementation of a digital filtering system the resolution approaches 130 eV. The system was operated with count rates up to 800 000 counts per second and per readout node, still conserving the spectroscopic qualities of the detector system.


Nuclear Instruments & Methods in Physics Research Section A-accelerators Spectrometers Detectors and Associated Equipment | 2001

Silicon drift detectors for high count rate X-ray spectroscopy at room temperature

P. Lechner; C. Fiorini; Robert Hartmann; J. Kemmer; Norbert Krause; P. Leutenegger; A. Longoni; Heike Soltau; D. Stötter; R. Stötter; L. Strüder; Ulrich Weber

Abstract Silicon Drift Detectors (SDDs) combine a large sensitive area with a small value of the output capacitance and are therefore well suited for high resolution, high count rate X-ray spectroscopy. The low leakage current level obtained by the elaborated processing technology makes it possible to operate them at room temperature or with moderate cooling. A brief description of the device principle is followed by the presentation of first results of a new production of large area SDDs with external electronics. Performance and applications of the already established SDDs with on-chip amplification are summarised. Various shapes of Multichannel Drift Detectors are introduced as well as their use in new experiments like X-ray holography and in new systems like an Anger camera for γ-ray imaging.


Optics Express | 2012

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

Andrew Aquila; Mark S. Hunter; R. Bruce Doak; Richard A. Kirian; Petra Fromme; Thomas A. White; Jakob Andreasson; David Arnlund; Sasa Bajt; Thomas R. M. Barends; Miriam Barthelmess; Michael J. Bogan; Christoph Bostedt; Hervé Bottin; John D. Bozek; Carl Caleman; Nicola Coppola; Jan Davidsson; Daniel P. DePonte; Veit Elser; Sascha W. Epp; Benjamin Erk; Holger Fleckenstein; Lutz Foucar; Matthias Frank; Raimund Fromme; Heinz Graafsma; Ingo Grotjohann; Lars Gumprecht; Janos Hajdu

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 time-resolved 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.


Nature Methods | 2012

In vivo protein crystallization opens new routes in structural biology

Rudolf Koopmann; Karolina Cupelli; Karol Nass; Daniel P. DePonte; Thomas A. White; Francesco Stellato; Dirk Rehders; Mengning Liang; Jakob Andreasson; Andrew Aquila; Sasa Bajt; Miriam Barthelmess; Anton Barty; Michael J. Bogan; Christoph Bostedt; Sébastien Boutet; John D. Bozek; Carl Caleman; Nicola Coppola; Jan Davidsson; R. Bruce Doak; Tomas Ekeberg; Sascha W. Epp; Benjamin Erk; Holger Fleckenstein; Lutz Foucar; Heinz Graafsma; Lars Gumprecht; J. Hajdu; Christina Y. Hampton

Protein crystallization in cells has been observed several times in nature. However, owing to their small size these crystals have not yet been used for X-ray crystallographic analysis. We prepared nano-sized in vivo–grown crystals of Trypanosoma brucei enzymes and applied the emerging method of free-electron laser-based serial femtosecond crystallography to record interpretable diffraction data. This combined approach will open new opportunities in structural systems biology.


Nature Methods | 2012

Lipidic phase membrane protein serial femtosecond crystallography.

Linda C. Johansson; David Arnlund; Thomas A. White; Gergely Katona; Daniel P. DePonte; Uwe Weierstall; R. Bruce Doak; Robert L. Shoeman; Lukas Lomb; Erik Malmerberg; Jan Davidsson; Karol Nass; Mengning Liang; Jakob Andreasson; Andrew Aquila; Sasa Bajt; Miriam Barthelmess; Anton Barty; Michael J. Bogan; Christoph Bostedt; John D. Bozek; Carl Caleman; Ryan Coffee; Nicola Coppola; Tomas Ekeberg; Sascha W. Epp; Benjamin Erk; Holger Fleckenstein; Lutz Foucar; Heinz Graafsma

X-ray free electron laser (X-FEL)-based serial femtosecond crystallography is an emerging method with potential to rapidly advance the challenging field of membrane protein structural biology. Here we recorded interpretable diffraction data from micrometer-sized lipidic sponge phase crystals of the Blastochloris viridis photosynthetic reaction center delivered into an X-FEL beam using a sponge phase micro-jet.


Nature | 2012

Fractal morphology, imaging and mass spectrometry of single aerosol particles in flight

N. D. Loh; Christina Y. Hampton; Andrew V. Martin; Dmitri Starodub; Raymond G. Sierra; A. Barty; Andrew Aquila; Joachim Schulz; Lukas Lomb; Jan Steinbrener; Robert L. Shoeman; Stephan Kassemeyer; Christoph Bostedt; John D. Bozek; Sascha W. Epp; Benjamin Erk; Robert Hartmann; Daniel Rolles; A. Rudenko; Benedikt Rudek; Lutz Foucar; Nils Kimmel; Georg Weidenspointner; G. Hauser; Peter Holl; Emanuele Pedersoli; Mengning Liang; M. M. Hunter; Lars Gumprecht; Nicola Coppola

The morphology of micrometre-size particulate matter is of critical importance in fields ranging from toxicology to climate science, yet these properties are surprisingly difficult to measure in the particles’ native environment. Electron microscopy requires collection of particles on a substrate; visible light scattering provides insufficient resolution; and X-ray synchrotron studies have been limited to ensembles of particles. Here we demonstrate an in situ method for imaging individual sub-micrometre particles to nanometre resolution in their native environment, using intense, coherent X-ray pulses from the Linac Coherent Light Source free-electron laser. We introduced individual aerosol particles into the pulsed X-ray beam, which is sufficiently intense that diffraction from individual particles can be measured for morphological analysis. At the same time, ion fragments ejected from the beam were analysed using mass spectrometry, to determine the composition of single aerosol particles. Our results show the extent of internal dilation symmetry of individual soot particles subject to non-equilibrium aggregation, and the surprisingly large variability in their fractal dimensions. More broadly, our methods can be extended to resolve both static and dynamic morphology of general ensembles of disordered particles. Such general morphology has implications in topics such as solvent accessibilities in proteins, vibrational energy transfer by the hydrodynamic interaction of amino acids, and large-scale production of nanoscale structures by flame synthesis.


Physical Review Letters | 2014

X-Ray Diffraction from Isolated and Strongly Aligned Gas-Phase Molecules with a Free-Electron Laser

Jochen Küpper; Stephan Stern; Lotte Holmegaard; Frank Filsinger; Arnaud Rouzée; Artem Rudenko; Per Johnsson; Andrew V. Martin; Marcus Adolph; Andrew Aquila; Sasa Bajt; Anton Barty; Christoph Bostedt; John D. Bozek; Carl Caleman; Ryan Coffee; Nicola Coppola; Tjark Delmas; Sascha W. Epp; Benjamin Erk; Lutz Foucar; Tais Gorkhover; Lars Gumprecht; Andreas Hartmann; Robert Hartmann; Günter Hauser; Peter Holl; André Hömke; Nils Kimmel; Faton Krasniqi

We report experimental results on x-ray diffraction of quantum-state-selected and strongly aligned ensembles of the prototypical asymmetric rotor molecule 2,5-diiodobenzonitrile using the Linac Coherent Light Source. The experiments demonstrate first steps toward a new approach to diffractive imaging of distinct structures of individual, isolated gas-phase molecules. We confirm several key ingredients of single molecule diffraction experiments: the abilities to detect and count individual scattered x-ray photons in single shot diffraction data, to deliver state-selected, e.g., structural-isomer-selected, ensembles of molecules to the x-ray interaction volume, and to strongly align the scattering molecules. Our approach, using ultrashort x-ray pulses, is suitable to study ultrafast dynamics of isolated molecules.


Nuclear Instruments & Methods in Physics Research Section A-accelerators Spectrometers Detectors and Associated Equipment | 2003

Design and technology of DEPFET pixel sensors for linear collider applications

R. Richter; Ladislav Andricek; P. Fischer; K. Heinzinger; Peter Lechner; G. Lutz; I. Peric; M. Reiche; G. Schaller; M. Schnecke; F. Schopper; Heike Soltau; L. Strüder; J. Treis; M. Trimpl; J. Ulrici; N. Wermes

The performance requirements of vertex detectors for future linear collider experiments is very challenging especially for the detectors innermost sensor layers. The DEPleted Field Effect Transistor (DEPFET) combining detector and amplifier operation is capable to meet these requirements. A silicon technology is presented which allows production of large sensor arrays consisting of linear DEPFET detector structures. The envisaged pixel array offers a low noise and low power operation. To ensure a high radiation length a thinning technology based on direct wafer bonding is proposed.

Collaboration


Dive into the Heike Soltau's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge