beamlines
Beamline AR-NW12A: high-throughput beamline for macromolecular crystallography at the Photon Factory
aStructural Biology Research Center, Photon Factory, High Energy Research Organization, 1-1 Oho, Tsukuba, Ibaraki 305-0801, Japan, and bInstitute for Protein Research, Osaka University, Osaka 565-0871, Japan
*Correspondence e-mail: leonard.chavas@kek.jp
AR-NW12A is an in-vacuum undulator beamline optimized for high-throughput macromolecular crystallography experiments as one of the five macromolecular crystallography (MX) beamlines at the Photon Factory. This report provides details of the beamline design, covering its optical specifications, hardware set-up, control software, and the latest developments for MX experiments. The experimental environment presents state-of-the-art instrumentation for high-throughput projects with a high-precision goniometer with an adaptable goniometer head, and a UV-light sample visualization system. Combined with an efficient automounting robot modified from the SSRL SAM system, a remote control system enables fully automated and remote-access X-ray diffraction experiments.
Keywords: macromolecular crystallography; high-throughput experiment; automated data collection; remote access; sample exchange robot.
1. Introduction
Located on the campus of the High Energy Accelerator Research Organization (KEK), the Photon Factory (PF) storage ring and the PF Advanced Ring (PF-AR) are operated as two synchrotron light sources. The PF-AR is a 6.5 GeV ring that was commissioned in 1984, converted to a dedicated synchrotron radiation source in 1998, and greatly upgraded in 2001. It currently accommodates eight beamlines, including the insertion-device beamline AR-NW12A, the oldest macromolecular crystallography (MX) beamline presently operational at KEK. AR-NW12A was constructed as an MX beamline mostly from an initial USD 6 million project as part of the 2001 upgrade scheme of the PF-AR Northwest Experimental Hall. The beamline was commissioned and then opened to users in May 2003, and has been operating as a high-throughput end-station since then. Academic users are being accommodated about 60% of the overall beam time available for the MX beamlines after being peer-reviewed by the PF Program Advisory Committee (PF-PAC). In recent years the number of users visiting MX beamlines has steadily increased, which can be reflected at AR-NW12A where 132 days of beam time were assigned in 2010, corresponding to a 36% gain compared with 2005.
2. Beamline overview
AR-NW12A is an MX beamline located at the PF-AR 6.5 GeV synchrotron source. The beamline was originally implemented as a high-throughput MX end-station, and subsequently equipped to accept multiple types of experimental environments, such as data collection of crystals with a size going down to 50 µm, crystals with large cell dimensions, and multiple/single-wavelength et al., 2012). AR-NW12A accepts 0.312 mrad (horizontal) × 0.029 mrad (vertical) of a 1.57 mm × 0.17 mm beam from a U#NW12 in-vacuum undulator comprising 95 periods, each of length 40 mm, and which can be operated at a minimum gap of 10.0 mm with Beff = 0.8 T. The sample position is located at 38.1 m from the light source, and exposed by a monochromatic beam in the energy range 6.5–17.7 keV with an energy resolution of about 2.5 × 10−4 (Table 1). The measured at the sample position at 12.39 keV is about 2.9 × 1011 photons s−1 for a typical beam size of 200 µm × 200 µm. Developed below are brief descriptions of each element along the beam path downstream of the undulator and up to the area detector, as shown in Fig. 1.
(MAD/SAD) experiments, and was recently expanded to adapt high-pressure crystallography set-ups (Nagae
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2.1. Interlock system and beam position monitors
A strict communication between a simple transmission and retrieval system (STARS) protocol-based beamline interlock control system (BLIS) (Kosuge et al., 2000) and the ring status allows a perfectly secured control of the beamline front-end, and notably of the main beam shutter (MBS). The BLIS checks each of the optical components in terms of temperature and vacuum level, and permits the opening of the MBS and subsequently of the downstream beam shutter (DSS) only if all the conditions are confirmed to be safe.
A set of horizontal and vertical wire monitors (H/VWM), five fluorescent screens (FS1–FS5), one gas-filled ion chamber (IC) and a silicon photodiode (PD) are arranged along the beam path. The H/VWMs and FSs are retractable and employed exclusively for beamline alignment purposes, to monitor the relative positions of the white beam and subsequently of the monochromatic beam (Fig. 1). Measurement of the is performed online using the IC located prior to the sample position, and the PD mounted on a retractable X-ray CCD detector shield, the latter being used only for fine beam alignments.
2.2. Mirrors and monochromator
Downstream from the white-beam slits (WBS) is located a vertical single-crystal collimating mirror (CM, flat shaped, 1 m long, rhodium-coated silicon) with a glancing angle of 3.5 mrad. Through mechanical bends, the water-cooled CM is used to collimate the incoming beam to the double-crystal monochromator (DCM), and diminishes in the meantime the heat load on the first crystal of the DCM generated by the 6.5 GeV PF-AR white beam. The collimated beam then passes through both crystals of the DCM prior to being focused by a toroidal single-crystal focusing mirror (FM, 1 m long, rhodium-coated silicon) with a glancing angle of 3.5 mrad. The focus point at the sample position is located at 11.1 m from the FM (demagnification of 2.44), and 38.1 m from the light source (Fig. 1). The DCM at AR-NW12A [numerical link type Si(111) crystals] was favored over other types of monochromators principally owing to its ease of use and capacity of maintaining the offset between the incoming and outcoming beam only by changing the gap between the two crystals when varying the energy. The two crystals are cooled using liquid nitrogen through an inline liquid-nitrogen cooling system (Suzuki Shokan) that allows an efficient temperature control and rapid response to changing heat loads.
Although most of the power of the strong incoming white beam is absorbed by the CM, and because of the current decrease of the PF-AR storage ring, the heat load on the first crystal of the DCM varies with time, causing changes in the crystal shape with local deformations, which is generally characterized by a shift in the beam height at the sample position. To limit this notorious effect, a piezo-electric device coupled with a beam-position feedback system was installed below the first DCM crystal. More precisely, a software-based feedback loop calculates the position of the beam passing through the IC and generates a proportional error signal digitally outputted to the piezo-controller (E-501.00; PI-Piezo) that in turn moves the piezo-motor (P-239.3SV; PI-Piezo) via a closed loop. This implementation allows continuous diffraction experiments for 12 h between beam injections with the beam position that remains unchanged within 20 µm.
2.3. Experimental environment
The experimental environment at AR-NW12A can be divided into three distinct areas. When arriving in the experimental hutch, the monochromatic beam is probed for its intensity and position by the IC, directly linked to the piezo-electric-based feedback system on the DCM to keep a constant beam position. Exiting from the IC, the beam passes through a beam attenuation unit, which consists of a series of aluminium foils of various thickness displayed on a motorized disk that provides an attenuated X-ray beam ranging from 0.1% to 100% depending on the beam energy. After the attenuator and preceding the beam shutter, two sets of quad-slits are used to shape the beam (typical size 200 µm × 200 µm).
Regrouped in a single box, most of the experimental environment apparatus directly operated by the users is arranged near the sample position (Fig. 2). Basically, all the various parts are retractable and can be mounted on demand, respecting some rules as to avoiding collision with other components. For instance, during data collection, the cryo-nozzle (CN), the guard slit (GS) and direct beam stopper (BS) are mounted, directly surrounding the sample; for experiments a Si-PIN diode detector (FD) comes near the sample, together with the GS; during crystal alignment, all components but the cold-light (CL) and eventually the UV-light (UVL) are removed. The GS removes unwanted parasitic scattering, and is made of a tantalum plate presenting a pinhole of 600 µm at its center. Downstream of the sample, two direct X-ray beam stoppers are provided. The front beam stopper (FBS) is mounted on a slender metal arm and aligned with the rotation axis to place the arm shadow within the cusp of the diffraction pattern. For particular set-ups that necessitate the full access of the space surrounding the sample position, such as the implementation of a diamond anvil cell (DAC) for high-pressure studies, a rear beam stopper (RBS) built as a fixed frame on the X-ray CCD detector is also available. Crystal centering is facilitated by a high-power (150 W) CL light emitted from a large flat panel, which has been optimized to allow visualization of the samples even during data collection without interfering with the diffraction experiment. A low-power (0.5 mW) 280 nm UVL can be mounted to help in the identification of the crystals [Fig. 3(a); Chavas et al., 2011]. The samples are cooled by a flow of cold nitrogen gas coming out of a GN2 cryo-system (Rigaku) that allows working under cryo-conditions down to 95 K. According to the operation requested, the distance between the sample and the exit of the CN is remotely controlled while keeping the temperature at the sample position unchanged.
Ensuring the proper alignment of the sample at the beam position, a cylinder of confusion of 2 µm is achieved with rotations around a single axis of a goniometer (Kohzu Precision). The adaptable goniometer head allows different types of sample holder to be accepted, including DACs (Chervin et al., 1995) for high-pressure experiments [Figs. 3(c)–3(d)]. Diffraction patterns are recorded on a Quantum 210r X-ray CCD camera (ADSC), with a sample-to-camera distance ranging from 60 to 950 mm. The CCD can be shifted vertically by 110 mm for high-resolution data collection up to 0.85 Å at a wavelength of 1 Å (Fig. 3b).
3. Ancillary facilities
All of the beamline control and data processing is performed from a control cabin, located adjacent to the experimental hutch. The cabin is also equipped with benches, microscopes and cryo-tools for sample preparation. An external laboratory is also at the disposition of the users, equipped with two temperature-controlled areas (277 and 293 K) for long-time sample conservation.
To favor an easy sample manipulation, a Standford Synchrotron Radiation Lightsource (SSRL)-type mounting robot (Cohen et al., 2002) called PAM (`PF automated mounting robot') was implemented at all the PF MX beamlines, and was recently upgraded to adapt the Gemini double-tongue system (Hiraki et al., 2008) and Universal pucks (Unipuck). By taking advantage of a large sample storage dewar, PAM is capable of mounting a total of 288 samples (3 SSRL cassettes of 96 sample holders) or 192 samples (12 Unipuk cassettes of 16 sample holders) continuously and undisturbed, without the need to access the experimental hutch. With an optimized data collection scheduling, and with the robot working at full regime, the sample exchange time goes down to 10 s (Hiraki et al., 2007).
All of the beamline components can be controlled via a unified GUI (UGUI) software developed on site. The software is constantly being ameliorated, and is implemented at all of the PF MX beamlines in a will to help users working in a friendly and exportable environment. UGUI is a Perl script base software that takes advantage of the STARS communication protocol to control all the hardware components of the beamline. Additionally, data processing and analysis software commonly used by protein crystallographers are available, including HKL2000 (Otwinowski & Minor, 1997), iMosflm (Battye et al., 2011), XDS (Kabsch, 1993), CCP4i (Collaborative Computational Project, Number 4, 1994), PHENIX (Adams et al., 2002), SHELX (Sheldrick, 2008) and other related programs.
4. Facility access
Evaluated based on their scientific merit and technical feasibility of the research plan, beam time application proposals to public beamlines of the PF can be submitted twice a year. Proposals are first reviewed by referees, and subsequently by members of the PF-PAC, who assign a ranking score used for prioritizing allocations.
For remote-access experiments, a dedicated so-called `external mode' has been implemented at AR-NW12A. The external mode takes advantage of the strict communication protocol that exists between the beamline shutters and the ring status through the BLIS to permit a safe control of the beamline. In addition, by accessing the UGUI beamline control software via a unique NoMachine NX session, users can fully run the beamline from their home laboratory just as if they were on site. Coupled with the PAM, the external access has obvious advantages for geographically remote users or even for teaching purposes.
5. Highlights
Commissioned in May 2003, AR-NW12A approaches its ten-year anniversary. Since its first users, the beamline has been extensively used both by academic users and pharmaceutical companies. As of January 2012, more than 540 coordinates were deposited in the Protein Data Bank for crystal structures of data collected at the beamline. Presented below is a non-exhaustive list of recent research results from the beamline, highlighting various types of experimental capabilities available at AR-NW12A.
5.1. MAD/SAD: PYL family signal regulator
The pyrabactin resistance-like (PYL) family of proteins are phytohormone abscisic acid (ABA) receptors that inhibit the activity of type-2C protein phosphatases in plants in response to ABA, action required for the proper regulation of the machinery for activating the drought-tolerance response in plants. The structure of the complex PYL–ABA was solved by the MAD method using selenium as the anomalous atom, at a resolution of 2.05 Å (Miyazono et al., 2009). This report is one of numerous studies performed at AR-NW12A that took advantage of MAD and SAD methods for structure determination.
5.2. High resolution: aristaless homeodomain
Accurate gene regulation is partly achieved by cooperative binding to DNA of homeodomain proteins, such as aristalless (Al) or clawless (Cll) DNA-binding proteins. To understand the regulation mechanism of such proteins, the ternary complex structure between Al, Cll and DNA, and that of the individual homeodomain proteins alone were solved, with the structure of the homeodomain Al that was refined to a resolution of 1.00 Å (Miyazono et al., 2010).
5.3. Large cell constants: bursal disease virus
In infectious bursal disease virus (IBDV), the viral protein VP2 constitutes part of the unenveloped icosahedral capsid and is the primary P213, with large cell dimensions of a = b = c = 316 Å (Lee et al., 2006).
The of VP2 was solved and refined at 2.6 Å resolution, providing essential insights into the mechanism by which VP2 spontaneously assembles to form the building block of IBDV (sub)viral particles. In these studies, 20 structurally heterogeneous protein subunits crystallized in the5.4. High-pressure studies: proteins from deep-sea organisms
Most of the enzymes originating from deep-sea organisms remain active at high pressures while related enzymes from land organisms lose their activity (Kato et al., 2008). To understand the pressure tolerance of proteins from deep-sea organisms, structural studies on several isopropylmalate dehydrogenase (IPDMH) from non-piezophile S.oneidensis MR-1 were performed at pressures ranging from atmospheric pressure to 650 MPa using a dedicated DAC (Nagae et al., 2012).
6. Discussion and conclusions
Considering the constant increase of proposal applications and requests for MX beam time, the need to implement fast data collection procedures with stable X-ray beams is of prime importance, and is well achieved at AR-NW12A. By taking advantage of our exceptionally quick and reliable mounting set-up (PAM equipped with the Gemini double-tongue system), the beamline could be fully automated and accept an even greater number of users for a shorter amount of beam time needed. With an averaged exposure time of 2 s per degree, a full data set of 180 frames with 1° oscillation angle could be collected in less than 10 min. Considering a time of 10 s for sample exchange when using our PAM system, a total of about 140 data sets could be collected in a 24 h shift (taking into account the time necessary to re-align the beam after the electron beam injection that occurs twice a day at PF-AR). The combined operation of the external mode with the remote access will facilitate unassisted data collection experiments from users located outside of the PF, which has clear advantages for geographically remote users.
To ease sample centering, notably during high-pressure experiments, an on-axis visualization system would be of indubitable value. Future developments at the beamline will also see the integration of a fully automated crystal centering procedure that exploits the specific properties of UV light. Together with the implementation of a decision-making strategy within the UGUI beamline control software, these developments will contribute to strengthening a pipeline for full automation of crystallographic experiments at all the PF MX beamlines.
Acknowledgements
The authors would like to thank the Photon Factory MX beamline crew. A part of this work was supported by Special Coordination Funds for Promoting Science and Technology (JSPS), Protein 3000 Project (MEXT), Targeted Proteins Research Program (MEXT), Grant-in-Aid for Young Scientists (JSPS).
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