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Publication
Featured researches published by Tamás Jávorfi.
Journal of Synchrotron Radiation | 2012
Rohanah Hussain; Tamás Jávorfi; Giuliano Siligardi
Synchrotron radiation circular dichroism (SRCD) is a well established technique in structural biology. The first UV-VIS beamline, dedicated to circular dichroism, at Diamond Light Source Ltd, a third-generation synchrotron facility in south Oxfordshire, UK, has recently become operational and it is now available for the user community. Herein the main characteristics of the B23 SRCD beamline, the ancillary facilities available for users, and some of the recent advances achieved are summarized.
Chirality | 2010
Tamás Jávorfi; Rohanah Hussain; Daniel Myatt; Giuliano Siligardi
Synchrotron radiation circular dichroism (SRCD) is a well-established method in structural biology. The first UV-VIS beamline dedicated to circular dichroism at Diamond Light Source, a third generation synchrotron facility in South Oxfordshire, has recently become operational and it is now available for the user community. Herein we present an important application of SRCD: the CD measurement of protein solutions in fused silica rectangular capillary cells. This was achieved without the use of any lens between the photoelastic modulator and the photomultiplier tube detectors by exploiting the high photon flux of the collimated beam that can be as little as half a millimeter squared. Measures to minimize or eliminate vacuum-UV protein denaturation effects are discussed. The CD spectra measured in capillaries is a proof of principle to address CD measurements in microdevice systems using the new B23 SRCD beamline.
Journal of Synchrotron Radiation | 2015
Rohanah Hussain; Kristian Benning; Tamás Jávorfi; Edoardo Longo; Timothy R. Rudd; Bill Pulford; Giuliano Siligardi
CDApps software at Diamond B23 SRCD beamline is presented.
Amino Acids | 2011
Emiliana De Santis; Thomas Hjelmgaard; Sophie Faure; Olivier Roy; Claude Didierjean; Bruce D. Alexander; Giuliano Siligardi; Rohanah Hussain; Tamás Jávorfi; Alison A. Edwards; Claude Taillefumier
The solution-phase synthesis and cyclisation of three α,β-peptoid octamers with differing side chain patterns is reported. One of these, compound C, showed a significantly greater resolution by NMR relative to the other two structurally related octamers. This observation was studied in detail by circular dichroism at a synchrotron light source to facilitate the correlation between the side chain patterns and conformational preference of these three peptoids. The X-ray crystal structure of cyclic octamer C, the first high-resolution structure for the α,β-peptoid backbone, was also obtained from methanol. Combined solid- and solution-phase studies allowed the identification of the N-2-(benzyloxy)ethyl side chain on the β-residue of the heterogeneous backbone as a key structural feature driving the increased conformational stability for octamer C.
Scientific Reports | 2015
Konstantin B. Borisenko; Janaki Shanmugam; Benjamin A.O. Williams; Paul Ewart; Behrad Gholipour; D.W. Hewak; Rohanah Hussain; Tamás Jávorfi; Giuliano Siligardi; Angus I. Kirkland
We demonstrate that optical activity in amorphous isotropic thin films of pure Ge2Sb2Te5 and N-doped Ge2Sb2Te5N phase-change memory materials can be induced using rapid photo crystallisation with circularly polarised laser light. The new anisotropic phase transition has been confirmed by circular dichroism measurements. This opens up the possibility of controlled induction of optical activity at the nanosecond time scale for exploitation in a new generation of high-density optical memory, fast chiroptical switches and chiral metamaterials.
Journal of Physical Chemistry B | 2018
Rohanah Hussain; Charlotte S. Hughes; Tamás Jávorfi; Giuliano Siligardi; Paul Williams; Boyan B. Bonev
Thermal unfolding of proteins is used extensively in screening of drug candidates because molecular interactions with ligands and substrates affect strongly protein stability, transition temperature, and cooperativity. We use synchrotron radiation circular dichroism to monitor the thermal evolution of secondary structure in proteins as they approach the melting point and the impact of substrate on their thermal behavior. Using Landau free energy expansion, we quantify transition strength and proximity to a critical point through the relative separation τ+ between the transition temperature Tm and the spinodal T+, obtained from the equation of state. The weakest transition was observed in lysozyme with τ+ = -0.0167 followed by holo albumin with τ+ = -0.0208 with the strongest transition in monomeric apo albumin τ+ = -0.0242. A structural transition at 45 °C in apo albumin leads to a noncooperative melt with τ+ = -0.00532 and amyloidogenic increase in beta content.
Scientific Reports | 2016
Rohanah Hussain; Tamás Jávorfi; Timothy R. Rudd; Giuliano Siligardi
The sample compartment for high-throughput synchrotron radiation circular dichroism (HT-SRCD) has been developed to satisfy an increased demand of protein characterisation in terms of folding and binding interaction properties not only in the traditional field of structural biology but also in the growing research area of material science with the potential to save time by 80%. As the understanding of protein behaviour in different solvent environments has increased dramatically the development of novel functions such as recombinant proteins modified to have different functions from harvesting solar energy to metabolonics for cleaning heavy and metal and organic molecule pollutions, there is a need to characterise speedily these system.
Journal of Physical Chemistry B | 2014
Václav Profant; Beata Seidlerová; Helena Dlouhá; Jana Hodačová; Tamás Jávorfi; Giuliano Siligardi; Vladimír Baumruk; Lucie Bednárová; Petr Maloň
Electronic circular dichroism (ECD) of the spirocyclic dilactam 5,8-diazatricyclo[6,3,0,0(1,5)]undecane-4,9-dione has been measured in the extended wavelength range (170-260 nm) utilizing far-UV CD instrumentation including synchrotron radiation light source. The data of this model of two nonplanar tertiary amide groups interacting within the rigid chiral environment provided new information particularly about the shorter wavelength π-π* transition region below 190 nm. The interpretation using TDDFT calculations confirmed that effects of amide nonplanarity follow our previous observations on monolactams as far as amide n-π* transitions are concerned. ECD band in the n-π* transition region of the nonplanar diamide exhibits an identical bathochromic shift and its sign remains tied to the sense of nonplanar deformation in the same way. As far as n-π* transitions are concerned amide nonplanarity acts as a local phenomenon independently reflecting sum properties of single amide groups. On the other hand, CD bands associated with π-π* transitions (found between ∼170 to 210 nm) form an exciton-like couplet with the sign pattern determined by mutual orientation of the associated electric transition moments. This sign pattern follows predictions pertaining to a coupled oscillator. The influence of amide nonplanarity on π-π* transitions is only minor and concentrates into the shorter wavelength lobe of the π-π* couplet. The detailed analysis of experimental ECD with the aid of TDDFT calculations shows that there is only little interaction between effects of inherent chirality caused by nonplanarity of amide groups and amide-amide coupling. Consequently these two effects can be studied nearly independently using ECD. In addition, the calculations indicate that participation of other type of transitions (n-σ*, π-σ* or Rydberg type transitions) is only minor and is concentrated below 180 nm.
Archive | 2011
E. De Santis; Thomas Hjelmgaard; Sophie Faure; Olivier Roy; Claude Didierjean; Bruce D. Alexander; Giuliano Siligardi; Rohanah Hussain; Tamás Jávorfi; Alison A. Edwards; Claude Taillefumier
Related Article: E.De Santis, T.Hjelmgaard, S.Faure, O.Roy, C.Didierjean, B.D.Alexander, G.Siligardi, R.Hussain, T.Javorfi, A.A.Edwards, C.Taillefumier|2011|Amino Acids|41|663|doi:10.1007/s00726-011-0887-1
Diamond Light Source Proceedings | 2011
Giuliano Siligardi; Rohanah Hussain; Daniel Myatt; Tamás Jávorfi
Circular dichroism spectroscopy is a useful and versatile tool to obtain low-resolution structural information about proteins, biopolymers and other chiral materials in solution. The first UV–VIS beamline dedicated to circular dichroism, B23, at Diamond Light Source Ltd., a third-generation synchrotron facility in the UK, has recently become operational and is now available for the user community. Herein we summarize the main characteristics of the beamline and some possible applications.