This website is being migrated. In case you don't find the information you are looking for, the old website can be found here. Thank you for reporting any anomalies to communication@ill.eu.
Switch instrument:
Virtual tour

BioSans

In the last decade, the number of high resolution protein structures has increased drastically as seen from the Protein Data Bank which contains now more than 30 000 structures. Tremendous progress in the automation of protein overproduction, crystallization, data collection and data treatment has facilitated the crystallographic studies of macromolecules. The challenge for the next decade is to integrate the molecular descriptions with their cellular environment. For this, structures of larger macromolecular complexes have to be deciphered. These multi-component complexes often participate in signal transduction pathways and have therefore dynamic structures that have to be unravelled by multiple approaches combining various resolutions and spatial scales.

Crystallographic approaches are very powerful in solving structures of proteins or macromolecular complexes at atomic resolution when they adopt well-defined conformations and can therefore be crystallized.More labile conformations, characteristic of modular proteins or transient complexes have to be characterized by other approaches. The combination of high-resolution techniques with low or medium resolution approaches leads to quasi-atomic models. This is well illustrated by several examples of virus structures where electron microscopy on single viruses provides for the overall viral envelope and X-ray crystallography of individual proteins leads to atomic structures that can be fitted into these envelopes. Small angle scattering has been used since several decades, although its use was very often limited to  very low resolution, the so-called Guinier region, analysis of which allows the determination of the radius of gyration and the molecular mass. In the last few years, experimental X-ray set-ups have improved and higher resolution scattering data are now exploitable.

Further mathematical developments made it possible to fit a molecular envelope to the interatomic distance distribution, the P(r) function, deduced from the small angle scattering data1. Small angle X-ray scattering is now a powerful tool for determining molecular envelopes that can be combined with high-resolution structures. In contrast to electron microscopy, the method can be used for smaller macromolecules and is therefore complementary. Neutron small angle scattering provides additional information for macromolecular complexes that are made of several types of molecules such as proteins, nucleic acids or lipids. Contrast variation experiments obtained by exchanging the solvent for deuterated or partially deuterated solvent enhances the signal from one component. SAXS and SANS are therefore tools of major importance in tackling systems biology.

Neutron small angle scattering instruments have been developed at ILL since several years and are available to the community. An X-ray small angle instrument is partially available for biological studies at ESRF, but does not respond to the increasing demand of the scientific community. This project aims to reinforce the development of small angle scattering for biological studies in general in Grenoble, by improving the instrumental facilities and helping in good quality data collection. It should also help in bridging the gap between the experimental data and the final molecular modeling in combination with X-ray or NMR partial structures.

References

  1. Petoukhov, M.V. & Svergun, D.I. (2005)
    Global rigid body modeling of macromolecular complexes against small-angle scattering data.
    Biophys J 89(2):1237-50.
    2.Svergun, D.I. & Koch, M.H.
    Advances in structure analysis using small-angle scattering in solution.
    Curr Opin Struct Biol 2002 12(5):654-60.
    3.Grizot S, Grandvaux N, Fieschi F, Faure J, Massenet C, Andrieu JP,  Fuchs A, Vignais PV, Timmins PA, Dagher, MC, Pebay-Peyroula E. (2001)
    Small angle neutron scattering and gel filtration analyses of neutrophil NADPH oxidase cytosolic factors highlight the role of the C-terminal end of p47(phox) in the association with p40(phox).
    Biochemistry.  40, 3127-33
    4. Durand, D., Cannella, D., Dubosclard, V., Pebay-Peyroula, E., Vachette, P., and Fieschi, F. (2006).
    Small-Angle X-Ray Scattering Study reveals an Extended Organization For The Auto-Inhibitory Resting State of the p47phox Modular Protein.
    Biochemistry  45, 7185-7193
    5. Gutsche I., Holzinger J., Rauh N., Baumeister W., May R.P. (2001)
    ATP-Induced Structural Change of the Thermosome Is Temperature-Dependent
    Journal of Structural Biology,  135, Number 2, 139-146(8)
    6. King W.A., Stone D.B., Timmins P.A., Narayanan T., von Brasch A.A.M., Mendelson R.A., Curmi P.M.G. (2005)
    Solution structure of the chicken skeletal muscle troponin complex via small-angle neutron and X-ray scattering
    J. Mol. Biol. 345, 797-815
    7. Heller, W.T., Finley, N, Wen-Ji D., Timmins, P., Cheung, H.C., Rosevear, P.R. and Trewhella, J (2003)
    Small-angle neutron scattering with contrast variation reveals spatial relationships between the three subunits in the ternary troponin complex and the effects of troponin I phosphorylation
    Biochemistry 42(25):7790-7800
    8. Fukuhara, N. Conti, E., Svergun, D., Petoukhov, P. and Timmins, P. (in preparation)
    Structure of the tRNA nuclear export complex
    9. Callow P., Timmins P. and Kneale G. (2006)
    Preliminary neutron scattering studies of the Type I restriction-modification enzyme M.Ahdl
    Physica B - Vol.385-386 - pp.853-855

by P. Timmins (ILL)

1) Getting beamtime (proposals, reports and deadlines): Access to beamtime at ESRF (http://www.esrf.eu/UsersAndScience/UserGuide/Applying) and ILL (http://www.ill.eu) is granted via electronic proposal systems. Potential users requesting beamtime must submit a scientific proposal online, providing scientific background on the experiments, description of the samples to be measured, time requested etc. The systems are generally open twice a year with deadlines that must be respected (at ESRF, there is a more frequent request of beamtime possible, the so-called rolling beamtime (http://www.esrf.eu/UsersAndScience/UserGuide/Applying/ProposalGuidelines/MXnon-BAGproposal/macromolecular-crystallography-rolling-applications)). In a proposal, a local contact that accompanies you during the experiment must be indicated in general. If successful, beamtime is generally attributed during the 6 months that follow the proposal deadline. The submitted proposals are reviewed by scientific committees that evaluate their scientific quality. Due to an overload factor that varies from instrument to instrument, not all proposals can be accepted. If beamtime has been granted, the users will be notified. Additional information about travel, accommodation and reimbursement can be found at the ILL and ESRF (http://www.esrf.eu/UsersAndScience/UserGuide).Joint SANS/SAXS proposals are possible; the request for additional SAXS beamtime must be indicated in your the ILL SANS proposal submission. If the SANS part of the proposal is accepted by the ILL subcommittee, you need to submit a request for the SAXS beamtime at ESRF (via the rolling beamtime system).2) Before the experiment (sample preparation and pre-characterization): The key to a successful SAXS/SANS experiment in biology is to know the biochemistry of the system studied. Prior to a SAXS/SANS experiment, as much information as possible should be collected on the system investigated by complementary methods. In the case of shape reconstruction, form factor analysis etc, monodisperse samples are needed (e.g. only one type of particle in solution). This should be checked by gel filtration, light scattering, SEC-MALLS, analytical ultracentrifugation, etc… The Partnership for Structural Biology (PSB) and the Partnership for Soft Condensed Matter (PSCM) offer a large variety of platforms for sample characterization (http://www.psb-grenoble.eu/spip.php?rubrique80 ; http://www.ill.eu/instruments-support/labs-facilities/pscm/soft-matter-laboratory/). If you need access to them, please do contact the platform responsibles well in advance of your scheduled SAXS/SANS experiments.The following points are particularly important:

  • Aggregation state: structural studies on aggregated samples are in general not possible, it is therefore essential to avoid aggregation. SANS practitioners should be aware that an elevated D2O content in the solution (as required for some experiments) may favor aggregation. In general, higher sample concentrations also favor aggregation. In such cases it is advisable to run a concentration series starting at higher concentrations (~10mg/ml) and going down to smaller concentrations (~1mg/ml). In the end, the highest concentrated sample that shows no aggregation is evaluated.
  • Concentration of the samples: concentrations for diluted samples measured by SAXS/SANS are typically situated in the range from 1-10 mg/ml (this corresponds to molarities of 0.05-0.5 mM for a 20 kDa system and 0.01-0.1 mM for a 100 kDa system). An accurate determination of the concentration prior to the experiments is also important for an absolute measurement of the molecular masses in solution by SANS. Concentrations should be known at an accuracy of about +/- 10%. In general, optical density measurements (e.g. at 280 nm for proteins) are more accurate than other assays (Bradford etc…).
  • Sample volumes required: Samples at the indicated concentrations are needed in ~200 µl volumes for SANS (generally measured in quartz cuvettes) and in smaller amounts (~50 µl ) for SAXS (capillary injection system).
  • Buffers: Buffers identical to the ones used with the samples (regarding salinity, pH, D2O content etc) need to be measured in order to subtract the background from the sample runs and to focus on the signal by the macromolecules in solution.
  • Concluding remarks regarding samples: For more detailed information, see Jeffries et al. Nature Protocols 11, 2122–2153 (2016). It is generally advisable to bring some backup samples to a SAXS/SANS experiment in the case that some samples do not behave properly (aggregation etc…) and to discuss sample conditions with your local contact.

3) During the experiment: Depending on the size of the macromolecules studied, the sample volume available, the temperature and pressure required, the instrument needs to be set up specifically.

  • Angular range (SANS): Collimator-sample and detector-sample distances need to be optimized against the size (i.e. presumed radius of gyration) of the macromolecules under investigation. If large objects are studied, these distances will generally be chosen large, if smaller objects and higher angular ranges are required, these distances will be chosen shorter.
  • Instrument calibration: Before measuring samples, the small angle scattering instrument needs to be calibrated at a given detector-collimator setup: centering of the incoming neutron/X-ray beam, determination of the detector efficiency, evaluation of the background noise and determination of the signal from the sample holder / capillary device.
  • Output of an experiment: The raw data from an experiment of an isotropically scattering system represent the scattering of the macromolecules in solution. They are generally corrected for the sample and instrument geometry, detector efficiency, electronic and buffer backgrounds, and averaged isotropically at a given angle. These operations are done by program suites that are specific for individual instruments.

4) After the experiment (sophisticated data treatment and interpretation):

  • Integral parameters: Integral parameters such as radii of gyration and molecular weights of the objects studied are available directly from the data as described above.
  • Modeling: The reduced raw data may be used to extract information going beyond radii of gyration and molecular weights. Several program suites are available to perform more sophisticated operations on the data (e.g. http://www.embl-hamburg.de/biosaxs/software.html). These include: extraction of a pair distribution function, ab intio low resolution modeling, rigid body modeling, etc.

Pérard J, Leyrat C, Baudin F, Drouet E, Jamin M. Structure of the full-length HCV IRES in solution. 
Nat Commun. 2013 Mar 19;4:1612. doi: 10.1038/ncomms2611. 

F. Spinozzi , P. Mariani, I. Mičetić, C. Ferrero, D. Pontoni, M. Beltramini, " Quaternary structure heterogeneity of oligomeric proteins: a SAXS and SANS study of the dissociation products of Octopus vulgaris hemocyanin”, PLoS One 11, e49644 (2012).

F. Spinozzi (a), P. Mariani (a), I. Mičetić (b,c), C. Ferrero (d), D. Pontoni (d), M. Beltramini (b),
Blue blood: a challenge for structural biologists. ESRF spotlight175 (2012). 

Leyrat C, Schneider R, Ribeiro EA Jr, Yabukarski F, Yao M, Gérard FC, Jensen MR, Ruigrok RW, Blackledge M, Jamin M. 
Ensemble structure of the modular and flexible full-length vesicular stomatitis virus phosphoprotein. 
J Mol Biol. 2012 Oct 19;423(2):182-97. 

E. Baldassarri Jr., M.G. Ortore, C. Ferrero, S. Finet, F. Spinozzi, P. Mariani, “Pressure effects on G-quadruplex structures stabilized by two different counter-ions”, International Review of Biophysical Chemistry (IREBIC), Vol. 2, N. 4, Special Section on 3rd International Meeting on G-Quadruplexes and G-assembly, p. 142, August 2011.