cshl 2015 shelxc/d/eshelx.uni-ac.gwdg.de/~athorn/pdf/thorn_cshl2015_shelxcde.pdf · theory....
TRANSCRIPT
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SHELXC/D/ECSHL 2015
Andrea Thorn
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• Single wavelength anomalous diffraction (SAD)• Native sulfur‐based SAD (S‐SAD)
• Multiple wavelength anomalous diffraction (MAD)• Single isomorphous replacement (SIR)
• Radiation‐induced phasing (RIP)• Multiple isomorphous replacement (MIR)• Single isomorphous replacement with anomalous scattering (SIRAS)
• Multiple isomorphous replacement with anomalous scattering (MIRAS)
Methods
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What is experimental phasing?
Experimental phasing methods depend on intensitydifferences.
These differences are caused by a marker substructureof certain elements.
MAD and SAD exploit the anomalous signal from one ormore data sets from the same crystal.
SIR (special case: RIP) and MIR utilizes several heavy‐atom soaked derivative crystals. They have to beisomorphous to be utilized.
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STRUCTURE FACTORSTheory
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Structure factors
For each reflection, there is a
structure factor Fhkl
If we know the structurefactors including theirphases for all reflections, wecan easily calculate theelectron density map, andhence get the structure.
Structure factors
Electron density
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Structure factors
structure factor Fhkl
= a wave
= a complex numberIm
Re
Amplitude = |Fhkl|
Phase = hkl
|Fhkl|2 ~ Ihkl Intensity
cannot be measured... :‐(
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Structure factors
Amplitude = |Fhkl|
Phase = hkl
|Fhkl|2 ~ Ihkl Intensity
cannot be measured... :‐( PHASE PROBLEM
The central problem of crystallography
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ANOMALOUS SCATTERINGTheory
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The anomalous signal
atomic scattering factor f
Im
Re
Each structure factor is composed of contributions f from each atom:
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The anomalous signal
Im
Re
Friedel‘s law: |Fhkl| = |F-h-k-l| hkl = --h-k-l
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The anomalous signal
But in reality, there is anomalous scattering due toresonance with electronic transitions in the atom:
f = f0 + f‘ + if‘‘
depends solely on resolution and element real component
imaginary component
f‘ and f‘‘ are observed near
absorption edges of the atom‘s element, and
are‐dependent
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The anomalous signal
f = f0 + f’ + i f ”
f '
f ''
E
Fluorescence scan orhttp://skuld.bmsc.washington.edu
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The anomalous signal
Im
Re
f'' breaks Friedel‘s law:
|Fhkl| |F-h-k-l|
hkl --h-k-l
f‘‘
The intensities ofFriedel pairs nolonger have thesame intensity!
This can be usedfor the absolutestructuredetermination andfor experimentalphasing!
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SUBSTRUCTURE SEARCH IN SHELXDHow to...
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Direct methods
• Phases of strong reflections are related (as a result ofthe non‐random distribution of atoms.)• Triplett equations• Sayre equation
• Relations are relatively easy to resolve for few atoms.• Usage of normalized structure factors (E values):
ε scale factor for propertreatment of specialposition reflections
<|Fhkl|2/ ε > mean per resolution shell
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Substructure search
Finding the substructure of marker atoms
• Direct methods• Patterson methods
• These methods require separate atomic electrondensities to locate atoms.
• They work here because the marker atoms havelarge interatomic distances.
• Disulfides become ‚supersulfurs‘.
Borrowed from small molecule crystallography
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Structure factors
Electron densityMap
Amplitudes& phases
Calculating a map ‐ Patterson
Intensities phases = 0
Patterson map
Intensity differences phases = 0
Anomalous Patterson
map
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Substructure search
• Patterson seeding: The Patterson map contains allinteratomic distance vectors between marker atoms.This can be used as a starting point (‚Pattersonseeding‘)
• Dual space direct methods recycle and modify trialsubstructures by peak search in the electron densityand refining phases in reciprocal space. Convergenceis faster than in reciprocal space alone.
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Substructure search
An overdetermined problem with noisy data...
Critical factors in substructure search:• Resolution range highly affects the outcome• Good data quality• Intensity outliers are problematic• Scaling (also anisotropic scaling) is needed
BEWARE: Handedness is not resolved at this stage!(Density modification differentiates later.)
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PHASING THE REST (SHELXC)How to...
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From substructure to structure
Im
Re
FP Protein contributionFA marker atom contributionFT = FP + FA
α = T - AA + α = T
We can combine all contributions from marker atoms into FA and everything else into FP.
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From substructure to structure
So, if we would know the anomalous scatterer positions (or heavy atom positions), we could calculate FA :
α = T - A
A + α = T
If we could then get α, we could calculate T and solve the phase problem!
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From substructure to structure
Phasing equations
sinα|F||F|ccosα|F||F|b|F|a|F||F| ATAT2
A2
T2
hkl
20
22 '''f
ffa
sinα|F||F|ccosα|F||F|b|F|a|F||F| ATAT2
A2
T2
lkh
0
'2ffb
0
''2ffc
AT
FT Total structure factorFA Marker substructure structure factor
If we would have no errors...
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From substructure to structure
Phasing equations
sinα|F||F|ccosα|F||F|b|F|a|F||F| ATAT2
A2
T2
hkl
sinα|F||F|ccosα|F||F|b|F|a|F||F| ATAT2
A2
T2
lkh
For each wavelength, we have different a, b, c and two observations. |FA|, |FT| and α are unknown. So given good data from at least two wavelengths, the equation can be solved. This would be MAD then, and works best if the f‘differences and the sum of f‘‘ values would be large!
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From substructure to structure
Phasing equations
sinα|F||F|ccosα|F||F|b|F|a|F||F| ATAT2
A2
T2
hkl
sinα|F||F|ccosα|F||F|b|F|a|F||F| ATAT2
A2
T2
lkh
In a SAD experiment, we have only two observables, as we measured only one wavelength. So we assume
|FT| = 0.5 (|Fhkl|+|F-h-k-l|) and get |Fhkl| - |F-h-k-l| = c|FA|sinα
This is sufficient for the substructure and estimation of φT!
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From substructure to structure
Im
Re
FP Protein contribution
FT (relates to Fhkl) = FP + FAFA = FA + FA‘ + FA‘‘Anomalous scatterer contribution
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From substructure to structure
Im
Re
This is what we know: |Fhkl| and |F-h-k-l|
|Fhkl|
|F-h-k-l|
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From substructure to structure
|Fhkl| >> |F-h-k-l|
Im
Re
|Fhkl|
|F-h-k-l|
This is what we know: |Fhkl| and |F-h-k-l|
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From substructure to structure
Im
Re
F+A‘‘
|Fhkl| >> |F-h-k-l|
F+A‘‘ has to point in thesame direction as |Fhkl|
F-A‘‘ has to point in theopposite direction as|F-h-k-l|
α must be close to 90°!
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From substructure to structure
Im
Re
F+A‘‘If: |Fhkl| << |F-h-k-l|
α must be close to270°!
Reflections with thelargest anomalousdifferences must beclosest to α = 90° orα=270°.
As you can easily see,estimation is rough.
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From substructure to structure
Im
Re
|Fhkl| |F-h-k-l|
F+A‘‘ and F-A‘‘ mustbe very small oralmost perpendicularto Fhkl or F-h-k-l,respectively.
α must be close to0° or 180°
|Fhkl|
|F-h-k-l|
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Density modification
• φT can now be computed from the phasing equations!
A + α = T
Via Fourier synthesis, an initial map is gained.
• By A coefficients and Sim weights the map is improved.
• But most important: Density modification is applied.
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DENSITY MODIFICATION IN SHELXEHow to...
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Density modification
Especially SAD phases are still ambiguous as well asinaccurate. Density modification dramatically improvesinitial phases, electron density and resolveshandedness!
• Based on areas filled by disordered solvent
• Solvent area is flattened or flipped
• NCS averaging can improve map quality
• High solvent content gives often better improvement
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Density modification
Most programs use a mask. SHELXE uses the sphere‐of‐influence method for density modification:
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Density modification
After several cycles, one of the two maps (one for eachsubstructure enantiomer) looks ‚like protein‘.
The other has less connectivity and looks ‚ragged‘.
After density modification, the structure is solved!Experimental phasing has led to initial phases.
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DENSITY MODIFICATION
Free lunch algorithm
Here, data is expanded with rough guesses for |Fhkl| to higher resolution (Typically from 2.0 Å downward).
This improves the density, because of:
• Correction of Fourier truncation errors
• Phases are the major influence
• 0 is a bad estimation for a not measured intensity.
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DENSITY MODIFICATION
After density modification (MapCC0.57), incomplete reflections to 1.3Å
After expansion to 1.0 (MapCC 0.94)
Usón et al, Acta Cryst. D63 (2007) 1069.
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PRACTICALITIESExperimental phasing, for real
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Data collection
• High multiplicity is good.
• Radiation damage is often bad.
• Precise intensity measurements are good.
• Near to the absorption edge, the crystal absorbs most energy, therefore radiation damage is high.
• A fluorescence scan can prove the presence of anomalous scatterers in the crystal.
• Good low resolution completeness
Pictures courtesy of Airlie McCoy
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Data collection: MAD
• Collect peak with at least multiplicity = 4.• Radiation damage? Stop and try SAD! Use a second crystal to collect high energy remote.
• No damage? Measure high energy remote.• Last data set should be inflection –so f‘ is maximized.
• A higher resolution data set with lower redundancy may prove useful for density modification and for refinement.
f = f0 + f’ + i f ”
f '
f ''
high
ene
rgyremote
peak
infle
ction po
int
E
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Data collection: SAD
• Best wavelength right and not tooclose to peak
• Beware not to hit the „white line“near the peak
• A bit away from peak, radiationdamage will be less
SAD data measured at peak are oftenthe result of a MAD experimentattempt!
f = f0 + f’ + i f ”
f '
f ''
here
E
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Data evaluation
• The general data quality should be good – multiplicity,completeness, RPIM etc.
• If scaling was applied, check statistics.• Check the mask; inner shell completeness?• Data set files well distinguishable?• If you have made a fluorescence scan, keep it.• Is there an anomalous signal in the collected data?
– Anomalous correlation within a data set: CCanom(1/2)
– <d”/σ> and/or <d’/σ>– Anomalous correlation of data sets: CCanom
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Things you want to have an idea about
• Space group? (Twinning?)• How many marker atoms do you expect?• Substructure: Which elements/molecules?• What could be the best resolution cut‐off?
(SHELXC assumes data resolution + 0.5Å)
• Could any marker atoms ‚fuse‘ into bigger blobs of density because of resolution cut‐off? Disulfides?
• Merging of data from different crystals/runs?• Expected solvent content and residue numbers?
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If you use SHELX...
SHELXC: α calculation, data analysis, file preparation
SHELXD: Substructure searchSHELXE: Density modification, tracing*
* A traced structure is solved; CC (trace against native data) > 25% (for data < 2.5 Å)
[ANODE: Validation]Pipeline?
Other experimental phasing programsshould be considered , in particular forease of use or problem cases**.
** http://strucbio.biologie.uni‐konstanz.de/ccp4wiki/index.php/Experimental_phasing
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SOFTWARE
The new SHELXE version (2013) also can do autotracing of the backbone.
A structure that can be traced is a structure solved*.
This proves particularly useful
• in borderline cases
• in pipelines, like ARCIMBOLDO or AUTORICKSHAW
* Solved: CC (trace against native data) > 25% for data < 2.5 Å!
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SOFTWARE
MR‐SAD
• Not enough phase information from SAD alone
or only partial Molecular Replacement solution
or severe model bias
• Use Molecular Replacement to bootstrap SAD phases
• (Partial) Molecular Replacement solution can be put into SHELXE, even without experimental differences
Schuermann & Tanner (2003). Acta Cryst. D59, 1731.
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ANOMALOUS MAPSANODE
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ANODE
• Structure validation
• Analysis of the
anomalous signal
Intensity differences & phases
Anomalous map
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Anomalous density mapsAnomalous density maps
at 3.5 σ
PDB 3FGD
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RIP density mapsRIP density maps
at 5.5σ/‐3.1σ
Nanao et al. (2005) Acta Crystallogr. D61, 1227
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RIP density mapsRIP density maps
at 4.8 σ / ‐3.1 σ
Nanao et al. (2005) Acta Crystallogr. D61, 1227
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SUMMARYFinal
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SUMMARY
• Experimental phasing methods use marker substructuresof certain elements to solve the phase problem via thephasing equations. Patterson maps can help.
• MAD and SAD exploit the anomalous signal from one ormore data sets from the same crystal.
• SIR and MIR utilizes several heavy‐atom soaked derivativecrystals. They have to be isomorphous to be utilized.
• Experimental phase solutions do not define theenantiomorph; after solution, the map that looks likeprotein has to be chosen!
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LITERATURE
• Bernhard Rupp, Biomolecular Crystallography: Principles, Practice, and Application to Structural Biology, 2004
• Kai Diederichs, P. Andrew Karplus, Improved R‐factors for diffraction data analysis in macromolecular crystallography. Nat Struct Biol. (1997). 4, 269‐75.
• Manfred S. Weiss, Global indicators of X‐ray data quality, J. Appl. Cryst. (2001). 34, 130‐135
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LITERATURE
• George M. Sheldrick, A short history of SHELX, ActaCryst. (2008). A64, 112‐122
• George M. Sheldrick (2002). Macromolecular phasing with SHELXE, Z. Kristallogr. 217:644‐650.
• George M. Sheldrick, Experimental phasing with SHELXC/D/E: combining chain tracing with density modification, Acta Cryst. (2010). D66, 479‐485
• A. Thorn & G.M. Sheldrick: “ANODE: ANOmalous and heavy‐atom DEnsity calculation” J. Appl. Cryst. 44 (2011), 1285‐1287More material: shelx.uni‐ac.gwdg.de/~athorn/
http://shelx.uni‐ac.gwdg.de/SHELX/
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ACKNOWLEDGEMENTS
I am grateful to George Sheldrick who freely shared with mehisknowledge, ideas and material. I also want to thank theMurshudov lab for their support!