Protein Crystallography
 
 
Cr-Phasing HomeLab
Crystallization
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A macromolecular home-lab X-ray system consists of five major components: X-ray generator, optics, area detector, software and crystal cryo-cooling system.

Rigaku offers options in all five areas so researchers can customize their lab to fit their experimental needs. Through years of experience, Rigaku has developed the expertise to easily integrate different technologies into a customized package that is 100% supported by the Rigaku organization.

Customers who purchase an X-ray system from Rigaku will receive the maximum flexibility in selecting components and also experience the benefits of full system responsibility from one company.

 
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Training Webinar
Taking the edge off: The softer side of in-house SAD phasing


Prof. John Rose
Presenters: Dr. Joe Ferrara and Prof. John Rose

Click here to view

Structure of the month

The structural charac­terization of the redundant thioredoxin system of Sulfolobus solfataricus


Cr-Phasing HomeLab
Phasing HomeLab featuring FR-E+ SuperBright source, helium cone, VariMax Cr optics and Rigaku IP detector
(click for larger picture)

Cr-Phasing HomeLab™

View the Cr phasing presentation 

View a slide presentation to learn how Cr phasing can contribute to the success of your protein structure determination program.

Anomalous scattering with soft X-ray radiation creates new possibilities in phasing for macromolecular crystallography. The heart of a Cr-Phasing HomeLab is any Rigaku rotating anode generator with a chromium anode..

All Rigaku rotating anode generators can be equipped with chromium (Cr) targets to provide the foundation for a Cr-Phasing HomeLab. All Cr-Phasing HomeLabs use the same optics and choice of large aperture detector. VariMax™ Cr optics maximize the beam produced by the Rigaku generators and deliver it exactly where it is needed: on the crystal. Incident and exit helium beam paths reduce air absorption and reduce background scatter. Since Cr radiation expands the diffraction pattern relative to Cu, a large aperture detector, such as the Rigaku R-AXIS IV++ or R-AXIS HTC, is recommended.

Source:

Any Rigaku rotating anode generator with Cr target
VariMax Cr optics

Detector: 

R-AXIS IV++ two-IP system
R-AXIS HTC three-IP system

Goniometer

Single φ (vertical or inverted) goniometer for R-AXIS detectors

Software:

CrystalClear™ for data collection and processing
StructureStudio™ for data collection
d*TREK® and HKL-2000® for data processing

Structures solved by Cr phasing at Nagoya University

Who should use Chromium radiation?

Investigators who wish to increase the throughput of de novo structure solution in their home laboratory. This would include investigators involved in the structural genomics initiative who wish to solve structures between synchrotron trips.

Chromium radiation (2.29 Å) doubles the available anomalous signal from elements such as S, Ca and Se as compared to the signal available with copper radiation (1.54 Å). This enhanced signal has allowed the structures of thaumatin and trypsin to solved using that signal with relatively small data sets, 45° and 180°, respectively. Work is currently progressing on the structure of glucose isomerase using only Cr radiation enhanced data.

A survey of the PDB shows the number de novo structures solved by MAD has been decreasing steadily since 2000. However, the number of SAD has been steadily increasing. 

The chromium radiation enhanced anomalous signal may also be used to augment SIRAS data that is insufficient to phase the data alone. In effect, using chromium radiation adds a second heavy atom, which concomitantly reduces the phase error and in turn yields more easily interpretable electron density maps. This procedure was essential to phase the structures of two proprietary proteins in our home lab.

ƒ" Cr (2.29 Å) Cu (1.54 Å)
Sulfur
1.14
0.56
Calcium
2.51
1.29
Selenium
2.28
1.14

Table 1. Increase in ƒ" for sulfur, calcium and selenium with chromium radiation versus copper radiation.

Radiation
Thaumatin Trypsin Glucose
isomerase
Cr Cu Cr Cu Cr Cu
Calculated
<ΔF>/<F> (%)
2.5 1.0 3.3 1.6 1.2 0.6
Observed
<ΔF>/<F> (%)
2.7 1.2 3.0 1.9 1.3 0.67

Table 2. Experimental improvement in <ΔF>/<F> thaumatin, trypsin and glucose isomerase for chromium radiation versus copper radiation.

How do you use Chromium radiation?

The best way to start using chromium radiation in your home lab is to upgrade your current facility. Current Rigaku rotating anode generator owners can easily convert to a Cr-Phasing HomeLab by adding a Cr anode and VariMax Cr optics.

Some Cr -SAD publications:

  • Yu Kitago, Nobuhisa Watanabe and Isao Tanaka, Structure determination of a novel protein by sulfur SAD using chromium radiation in combination with a new crystal-mounting method, Acta Cryst. (2005). D61, 1013-1021
  • Acta Crystallogr D Biol Crystallogr. 2003 Nov;59(Pt 11):1943-57. Epub 2003 Oct 23. Away from the edge: SAD phasing from the sulfur anomalous signal measured in-house with chromium radiation.
  • Acta Crystallogr D Biol Crystallogr. 2005 Jul;61(Pt 7):960-6. Epub 2005 Jun 24. Away from the edge II: in-house Se-SAS phasing with chromium radiation.
  • Acta Crystallogr D Biol Crystallogr. 2005 Aug;61(Pt 8):1013-21. Epub 2005 Jul 20. Structure determination of a novel protein by sulfur SAD using chromium radiation in combination with a new crystal-mounting method.
  • Acta Crystallogr D Biol Crystallogr. 2005 Jul;61(Pt 7):960-6. Epub 2005 Jun 24. Away from the edge II: in-house Se-SAS phasing with chromium radiation.