Techert, Simone

[["dc.bibliographiccitation.artnumber","129302"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Physical Review Letters"],["dc.bibliographiccitation.volume","112"],["dc.contributor.author","Föhlisch, A."],["dc.contributor.author","de Groot, F. M. F."],["dc.contributor.author","Odelius, M."],["dc.contributor.author","Techert, S."],["dc.contributor.author","Wernet, P."],["dc.date.accessioned","2022-12-15T10:55:26Z"],["dc.date.available","2022-12-15T10:55:26Z"],["dc.date.issued","2014-03-28"],["dc.identifier.doi","10.1103/PhysRevLett.112.129302"],["dc.identifier.pmid","24724687"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/118746"],["dc.language.iso","en"],["dc.relation.eissn","1079-7114"],["dc.relation.issn","0031-9007"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.title","Comment on \"State-dependent electron delocalization dynamics at the solute-solvent interface: soft-x-ray absorption spectroscopy and ab initio calculations\""],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","letter_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","109"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","The European Physical Journal E - Soft Matter"],["dc.bibliographiccitation.volume","36"],["dc.contributor.author","Jain, R."],["dc.contributor.author","Petri, M."],["dc.contributor.author","Kirschbaum, S."],["dc.contributor.author","Feindt, H."],["dc.contributor.author","Steltenkamp, Siegfried"],["dc.contributor.author","Sonnenkalb, S."],["dc.contributor.author","Becker, S."],["dc.contributor.author","Griesinger, Christian"],["dc.contributor.author","Menzel, A."],["dc.contributor.author","Burg, T. P."],["dc.contributor.author","Techert, S."],["dc.date.accessioned","2017-09-07T11:47:08Z"],["dc.date.available","2017-09-07T11:47:08Z"],["dc.date.issued","2013"],["dc.description.abstract","Small-angle X-ray scattering provides global, shape-sensitive structural information about macromolecules in solution. Its extension to time dimension in the form of time-resolved SAXS investigations and combination with other time-resolved biophysical methods contributes immensely to the study of protein dynamics. TR-SAXS can also provide unique information about the global structures of transient intermediates during protein dynamics. An experimental set-up with low protein consumption is essential for an extensive use of TR-SAXS experiments on protein dynamics. In this direction, a newly developed 20-microchannel microfluidic continuous-flow mixer was combined with SAXS. With this set-up, we demonstrate ubiquitin unfolding dynamics after rapid mixing with the chaotropic agent Guanidinium-HCl within milliseconds using only similar to 40 nanoliters of the protein sample per scattering image. It is suggested that, in the future, this new TR-SAXS platform will help to increase the use of time-resolved small-angle X-ray scattering, wide-angle X-ray scattering and neutron scattering experiments for studying protein dynamics in the early millisecond regime. The potential research field for this set-up includes protein folding, protein misfolding, aggregation in amyloidogenic diseases, function of intrinsically disordered proteins and various protein-ligand interactions."],["dc.identifier.doi","10.1140/epje/i2013-13109-9"],["dc.identifier.gro","3142281"],["dc.identifier.isi","000325224100001"],["dc.identifier.pmid","24092048"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/6542"],["dc.notes.intern","WoS Import 2017-03-10 / Funder: Nanoscale Photon Imaging of the DFG [SFB 755]"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation.issn","1292-8941"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.title","X-ray scattering experiments with high-flux X-ray source coupled rapid mixing microchannel device and their potential for high-flux neutron scattering investigations"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5700"],["dc.bibliographiccitation.issue","24"],["dc.bibliographiccitation.journal","The Journal of Physical Chemistry A"],["dc.bibliographiccitation.lastpage","5710"],["dc.bibliographiccitation.volume","104"],["dc.contributor.author","Techert, Simone"],["dc.contributor.author","Schmatz, S."],["dc.contributor.author","Wiessner, A."],["dc.contributor.author","Staerk, H."],["dc.date.accessioned","2018-11-07T10:44:05Z"],["dc.date.available","2018-11-07T10:44:05Z"],["dc.date.issued","2000"],["dc.description.abstract","Experimental and theoretical investigations of the spectroscopic properties have been carried out on three charge-transfer model systems, covalently linked donor-acceptor compounds of the type pyrene and derivatives of N,N-dimethylaniline (dimethyl(4-pyren-1-ylphenyl)amine (PyDMA), dimethyl(3-methyl-4-pyren-1-ylphenyl)amine (PyMDMA), and (3,5-dimethyl-4-pyren-1-ylphenyl)dimethylamine (PyDMDMA)). Comparing stationary absorption and emission spectra as well as fluorescence lifetimes in different solvents, one can show that small chemical changes such as substitution of ortho-hydrogens by methyl groups on the DMA moiety introduces dramatic effects in spectroscopic and kinetic behavior. On the basis of infrared measurements and quantum chemical calculations, the experiments are interpreted within a statistical framework, with particular emphasis on the discussion of preferred large amplitude motion (twist angle) and pyrene-specific vibronic coupling."],["dc.identifier.doi","10.1021/jp9935384"],["dc.identifier.isi","000087782800004"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/47194"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","1089-5639"],["dc.title","Photophysical characteristics of directly linked pyrene-dimethylaniline derivatives"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","57"],["dc.bibliographiccitation.journal","Faraday Discussions"],["dc.bibliographiccitation.lastpage","80"],["dc.bibliographiccitation.volume","171"],["dc.contributor.author","Boll, Rebecca"],["dc.contributor.author","Rouzee, Arnaud"],["dc.contributor.author","Adolph, Marcus"],["dc.contributor.author","Anielski, Denis"],["dc.contributor.author","Aquila, Andrew"],["dc.contributor.author","Bari, Sadia"],["dc.contributor.author","Bomme, Cedric"],["dc.contributor.author","Bostedt, Christoph"],["dc.contributor.author","Bozek, John D."],["dc.contributor.author","Chapman, Henry N."],["dc.contributor.author","Christensen, Lauge"],["dc.contributor.author","Coffee, Ryan"],["dc.contributor.author","Coppola, Niccola"],["dc.contributor.author","De, Sankar"],["dc.contributor.author","Decleva, Piero"],["dc.contributor.author","Epp, Sascha W."],["dc.contributor.author","Erk, Benjamin"],["dc.contributor.author","Filsinger, Frank"],["dc.contributor.author","Foucar, Lutz"],["dc.contributor.author","Gorkhover, Tais"],["dc.contributor.author","Gumprecht, Lars"],["dc.contributor.author","Hoemke, Andre"],["dc.contributor.author","Holmegaard, Lotte"],["dc.contributor.author","Johnsson, Per"],["dc.contributor.author","Kienitz, Jens S."],["dc.contributor.author","Kierspel, Thomas"],["dc.contributor.author","Krasniqi, Faton"],["dc.contributor.author","Kuehnel, Kai-Uwe"],["dc.contributor.author","Maurer, Jochen"],["dc.contributor.author","Messerschmidt, Marc"],["dc.contributor.author","Moshammer, Robert"],["dc.contributor.author","Mueller, Nele L. M."],["dc.contributor.author","Rudek, Benedikt"],["dc.contributor.author","Savelyev, Evgeny"],["dc.contributor.author","Schlichting, Ilme"],["dc.contributor.author","Schmidt, Carlo"],["dc.contributor.author","Scholze, Frank"],["dc.contributor.author","Schorb, Sebastian"],["dc.contributor.author","Schulz, Joachim"],["dc.contributor.author","Seltmann, Joern"],["dc.contributor.author","Stener, Mauro"],["dc.contributor.author","Stern, Stephan"],["dc.contributor.author","Techert, Simone"],["dc.contributor.author","Thogersen, Jan"],["dc.contributor.author","Trippel, Sebastian"],["dc.contributor.author","Viefhaus, Jens"],["dc.contributor.author","Vrakking, Marc"],["dc.contributor.author","Stapelfeldt, Henrik"],["dc.contributor.author","Kuepper, Jochen"],["dc.contributor.author","Ullrich, Joachim"],["dc.contributor.author","Rudenko, Artem"],["dc.contributor.author","Rolles, Daniel"],["dc.date.accessioned","2018-11-07T09:45:38Z"],["dc.date.available","2018-11-07T09:45:38Z"],["dc.date.issued","2014"],["dc.description.abstract","This paper gives an account of our progress towards performing femtosecond time-resolved photoelectron diffraction on gas-phase molecules in a pump-probe setup combining optical lasers and an X-ray free-electron laser. We present results of two experiments aimed at measuring photoelectron angular distributions of laser-aligned 1-ethynyl-4-fluorobenzene (C8H5F) and dissociating, laser-aligned 1,4-dibromobenzene (C6H4Br2) molecules and discuss them in the larger context of photoelectron diffraction on gas-phase molecules. We also show how the strong nanosecond laser pulse used for adiabatically laser-aligning the molecules influences the measured electron and ion spectra and angular distributions, and discuss how this may affect the outcome of future time-resolved photoelectron diffraction experiments."],["dc.identifier.doi","10.1039/c4fd00037d"],["dc.identifier.isi","000345529900003"],["dc.identifier.pmid","25290160"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/34670"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","1364-5498"],["dc.relation.issn","1359-6640"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.title","Imaging molecular structure through femtosecond photoelectron diffraction on aligned and oriented gas-phase molecules"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","10187"],["dc.bibliographiccitation.issue","29"],["dc.bibliographiccitation.journal","Physical Chemistry, Chemical Physics"],["dc.bibliographiccitation.lastpage","10195"],["dc.bibliographiccitation.volume","14"],["dc.contributor.author","Moré, René"],["dc.contributor.author","Scholz, Mirko"],["dc.contributor.author","Busse, Gehard"],["dc.contributor.author","Busse, Lennart"],["dc.contributor.author","Paulmann, Carsten"],["dc.contributor.author","Tolkiehn, Martin"],["dc.contributor.author","Techert, Simone"],["dc.date.accessioned","2022-12-16T09:15:15Z"],["dc.date.available","2022-12-16T09:15:15Z"],["dc.date.issued","2012-08-07"],["dc.description.abstract","We compare results from single crystal X-ray diffraction and FTIR spectroscopy to elucidate the nature of hydrogen bonding in β-9-anthracene carboxylic acid (β-9AC, C(15)H(10)O(2)). The crystallographic studies indicate a disorder for the protons in the cyclic hydrogen bond. This disorder allows the determination of the energy difference between two proton sites along the hydrogen bond. The temperature dependent Fourier transform infrared spectroscopy (FTIR) underpins the crystallographic results. The combination of both methods allows the estimation of a one-dimensional potential curve describing the OH-stretching motion. The dynamical properties of the proton transfer along the hydrogen bond are extracted from this potential. The work presented here has profound implication on future studies of photochemical dynamics of crystalline β-9AC, which can deliver a deeper understanding of the mechanism of photochemical driven molecular machines and the optical and electronic properties of molecular organic semiconductors."],["dc.identifier.doi","10.1039/c2cp40216e"],["dc.identifier.pmid","22735829"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/118801"],["dc.language.iso","en"],["dc.relation.eissn","1463-9084"],["dc.relation.issn","1463-9076"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.title","Hydrogen bond dynamics in crystalline β-9-anthracene carboxylic acid--a combined crystallographic and spectroscopic study"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]

[["dc.contributor.author","Basuroy, Krishnayan"],["dc.contributor.author","Velazquez Garcia, Jose"],["dc.contributor.author","Gosztola, David"],["dc.contributor.author","Techert, Simone"],["dc.date.accessioned","2022-12-14T07:55:52Z"],["dc.date.available","2022-12-14T07:55:52Z"],["dc.date.issued","2021"],["dc.description.abstract","Pyrene based molecules are inclined to form excimers through self-association upon photoexcitation. In this work, the pyrene core is functionalized with N-methylacetamide group at the position 1 or 2, to develop pyren-1-methylacetamide (PyMA1) and pyren-2-methylacetamide (PyMA2), respectively. Upon photoexcitation, PyMA1 and PyMA2, at 1.0mM,in toluene, have formed predominantly static excimers. The steady state spectroscopic studies have showed that the excitonic coupling of PyMA1 dimers are much stronger in solution than its isomeric counterpart, PyMA2. The transient absorption (TA) measurements over fs-ps regime (fs-TA) showed that the formation of static excimers with the strongly-coupled pre-associated dimers, in PyMA1, happens in approx. 560fs, whereas, the excimers for the weakly-coupled pre-associated dimers in PyMA2 have formed in much slower time scale (approx. 65ps). The introduction of methylacetamide group at the position 1 or 2 on pyrene ring, was believed to have allowed forming hydrogen bonded excimers with different degrees of excitonic coupling."],["dc.identifier.doi","10.3204/PUBDB-2021-01571"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/118615"],["dc.language.iso","en"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.title","Ultrafast Processes in Isomeric Pyrene-N-methylacetamides: Formation of Hydrogen Bond Induced Static Excimers with Varied Coupling Strength"],["dc.type","preprint"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","7579"],["dc.bibliographiccitation.issue","31"],["dc.bibliographiccitation.journal","The Journal of Physical Chemistry B"],["dc.bibliographiccitation.lastpage","7587"],["dc.bibliographiccitation.volume","105"],["dc.contributor.author","Techert, Simone"],["dc.contributor.author","Wiessner, A."],["dc.contributor.author","Schmatz, S."],["dc.contributor.author","Staerk, H."],["dc.date.accessioned","2018-11-07T08:45:55Z"],["dc.date.available","2018-11-07T08:45:55Z"],["dc.date.issued","2001"],["dc.description.abstract","Picosecond transient absorption spectroscopy and picosecond spectro-streak fluorescence measurements have been carried out in order to understand the complex photophysical dynamics of directly linked donor-acceptor systems and the solvation dynamics in longer-chain alcohols. With these techniques, the fast solvent response to optically generated charge transfer (CT) species can be followed. Studies were performed on covalently linked donor-acceptor systems of the type pyrene with derivatives of N,N-dimethylaniline: dimethyl-(4-pyren-1-yl-phenyl)-amine, dimethyl-(3-methyl-4-pyren-1-yl-phenyl)-amine and (3,5-dimethyl-4-pyren-1-yl-phenyl)-dimethylamine. The results are interpreted with particular emphasis on solvation dependent electronic restructuring of the CT species. We suggest a mechanism where the adiabatic electronic restructuring coincides with the coupling to the torsional degrees of freedom of the solvent."],["dc.identifier.doi","10.1021/jp004370l"],["dc.identifier.isi","000170300100028"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/20563"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","1089-5647"],["dc.title","Time-resolved fluorescence and solvatochromy of directly linked pyrene-DMA derivatives in alcoholic solution"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","014301"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Structural Dynamics"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Amini, Kasra"],["dc.contributor.author","Savelyev, Evgeny"],["dc.contributor.author","Brauße, Felix"],["dc.contributor.author","Berrah, Nora"],["dc.contributor.author","Bomme, Cédric"],["dc.contributor.author","Brouard, Mark"],["dc.contributor.author","Burt, Michael"],["dc.contributor.author","Christensen, Lauge"],["dc.contributor.author","Düsterer, Stefan"],["dc.contributor.author","Erk, Benjamin"],["dc.contributor.author","Höppner, Hauke"],["dc.contributor.author","Kierspel, Thomas"],["dc.contributor.author","Krecinic, Faruk"],["dc.contributor.author","Lauer, Alexandra"],["dc.contributor.author","Lee, Jason W. L."],["dc.contributor.author","Müller, Maria"],["dc.contributor.author","Müller, Erland"],["dc.contributor.author","Mullins, Terence"],["dc.contributor.author","Redlin, Harald"],["dc.contributor.author","Schirmel, Nora"],["dc.contributor.author","Thøgersen, Jan"],["dc.contributor.author","Techert, Simone"],["dc.contributor.author","Toleikis, Sven"],["dc.contributor.author","Treusch, Rolf"],["dc.contributor.author","Trippel, Sebastian"],["dc.contributor.author","Ulmer, Anatoli"],["dc.contributor.author","Vallance, Claire"],["dc.contributor.author","Wiese, Joss"],["dc.contributor.author","Johnsson, Per"],["dc.contributor.author","Küpper, Jochen"],["dc.contributor.author","Rudenko, Artem"],["dc.contributor.author","Rouzée, Arnaud"],["dc.contributor.author","Stapelfeldt, Henrik"],["dc.contributor.author","Rolles, Daniel"],["dc.contributor.author","Boll, Rebecca"],["dc.date.accessioned","2019-07-09T11:45:24Z"],["dc.date.available","2019-07-09T11:45:24Z"],["dc.date.issued","2018"],["dc.description.abstract","We explore time-resolved Coulomb explosion induced by intense, extreme ultraviolet (XUV) femtosecond pulses from a free-electron laser as a method to image photo-induced molecular dynamics in two molecules, iodomethane and 2,6-difluoroiodobenzene. At an excitation wavelength of 267 nm, the dominant reaction pathway in both molecules is neutral dissociation via cleavage of the carbon-iodine bond. This allows investigating the influence of the molecular environment on the absorption of an intense, femtosecond XUV pulse and the subsequent Coulomb explosion process. We find that the XUV probe pulse induces local inner-shell ionization of atomic iodine in dissociating iodomethane, in contrast to non-selective ionization of all photofragments in difluoroiodobenzene. The results reveal evidence of electron transfer from methyl and phenyl moieties to a multiply charged iodine ion. In addition, indications for ultrafast charge rearrangement on the phenyl radical are found, suggesting that time-resolved Coulomb explosion imaging is sensitive to the localization of charge in extended molecules."],["dc.identifier.doi","10.1063/1.4998648"],["dc.identifier.pmid","29430482"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/15198"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/59224"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation","info:eu-repo/grantAgreement/EC/FP7/238671/EU//ICONIC"],["dc.relation","info:eu-repo/grantAgreement/EC/H2020/641789/EU//MEDEA"],["dc.relation","info:eu-repo/grantAgreement/EC/FP7/614507/EU//COMOTION"],["dc.relation.issn","2329-7778"],["dc.relation.orgunit","Fakultät für Physik"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0/"],["dc.subject.ddc","530"],["dc.title","Photodissociation of aligned CH3I and C6H3F2I molecules probed with time-resolved Coulomb explosion imaging by site-selective extreme ultraviolet ionization."],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","10996"],["dc.bibliographiccitation.issue","36"],["dc.bibliographiccitation.journal","The Journal of Physical Chemistry. B, Condensed Matter, Materials, Surfaces, Interfaces & Biophysical"],["dc.bibliographiccitation.lastpage","11003"],["dc.bibliographiccitation.volume","116"],["dc.contributor.author","Hallmann, Jörg"],["dc.contributor.author","More, Rene"],["dc.contributor.author","Morgenroth, Wolfgang"],["dc.contributor.author","Paulmann, Carsten"],["dc.contributor.author","Kong, Qingyu"],["dc.contributor.author","Wulff, Michael"],["dc.contributor.author","Techert, Simone"],["dc.date.accessioned","2022-12-16T09:14:19Z"],["dc.date.available","2022-12-16T09:14:19Z"],["dc.date.issued","2012-09-13"],["dc.description.abstract","Time-resolved diffuse X-ray scattering is one powerful method for monitoring the progression from the creation of local structural changes inside a crystalline material up to the transformation of the whole crystalline bulk. In this work, we study the mechanism of phototransformation of a molecular crystal by time-resolved diffuse X-ray scattering. Here, an optical excitation source, like a pulsed laser, initiates structural transformations which are monitored by X-ray scattering techniques. We have studied the dimerization process of the molecular switch α-styrylpyrylium (trifluoromethanesulfonate) TFMS, in particular for understanding whether cooperative effects influence the changes of the structure in the bulk and its periodicity. Upon illumination with optical light, α-styrylpyrylium TFMS instantaneously photoswitches. Depending on the optical fluence, X-ray diffuse planes are observed prior to phototransformation of the bulk. In the early stages of transformation, the analysis reveals systems of randomly distributed islands of product clusters with gradual growth in size and amount. The degree of transformation follows the optical excitation profile, i.e., the spatial absorption of the laser beam. In the present studies, no influence of cooperativity on the photodimerization process has been found."],["dc.identifier.doi","10.1021/jp3020832"],["dc.identifier.pmid","22934959"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/118791"],["dc.language.iso","en"],["dc.relation.eissn","1520-5207"],["dc.relation.issn","1520-6106"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.title","Evidence for point transformations in photoactive molecular crystals by the photoinduced creation of diffuse diffraction patterns"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","242"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Protein and Peptide Letters"],["dc.bibliographiccitation.lastpage","254"],["dc.bibliographiccitation.volume","23"],["dc.contributor.author","Jain, Rohit"],["dc.contributor.author","Techert, Simone"],["dc.date.accessioned","2018-11-07T10:20:39Z"],["dc.date.available","2018-11-07T10:20:39Z"],["dc.date.issued","2016"],["dc.description.abstract","X-ray scattering technique, comprising of small-angle/wide-angle X-ray scattering (SAXS/WAXS) techniques is increasingly used to characterize the structure and interactions of biological macromolecules and their complexes in solution. It is a method of choice to characterize the flexible, partially folded and unfolded protein systems. X-ray scattering is the last resort for proteins that cannot be investigated by crystallography or NMR and acts as a complementary technique with different biophysical techniques to answer challenging scientific questions. The marriage of the X-ray scattering technique with the fourth dimension \"time\" yields structural dynamics and kinetics information for protein motions in hierarchical timescales from picoseconds to days. The arrival of the high-flux X-ray beam at third generation synchrotron sources, exceptional X-ray optics, state-of-the-art detectors, upgradation of X-ray scattering beamlines with microfluidics devices and advanced X-ray scattering data analysis procedures are the important reasons behind the shining years of X-ray scattering technique. The best days of the X-ray scattering technique are on the horizon with the advent of the nanofocus X-ray scattering beamlines and fourth generation X-ray lightsources, i.e., free electron lasers (XFELs). Complementary to the photon-triggered time-resolved X-ray scattering techniques, we will present an overview of the time-resolved and in-situ X-ray scattering techniques for structural dynamics of ubiquitous non-photoactive proteins."],["dc.description.sponsorship","Helmholtz Society; Max Planck Society; [SFB 755]"],["dc.identifier.doi","10.2174/0929866523666160106153847"],["dc.identifier.isi","000373714100006"],["dc.identifier.pmid","26732244"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/41930"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","1875-5305"],["dc.relation.issn","0929-8665"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.relation.workinggroup","RG Techert (Structural Dynamics in Chemical Systems)"],["dc.title","Time-Resolved and In-Situ X-Ray Scattering Methods Beyond Photoactivation: Utilizing High-Flux X-Ray Sources for the Study of Ubiquitous Non-Photoactive Proteins"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]