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Manual |
X-RaY crystallography FACILITY, Kasha Laboratory
Institute of Molecular Biophysics
Data Collection & Processing Guide
Macromolecular x-Ray Facility Crystallography Facility
Data Collection & Processing Guide
Copyright ã 2000-2004 Thayumanasamy Somasundaram
410-414 Kasha Laboratory • Institute of Molecular Biophysics
E-mail: soma@sb.fsu.edu
• URL: http://www.sb.fsu.edu/~soma
Phone 850.644.6448 • Fax 850.644.7244
September 28, 2004
Table of Contents
Introduction i
Purchase Orders & Blanket Orders
3. Regular data collection procedure
IP (Windows
NT, anaconda.chem.fsu.edu)
CCD (Linux,
spruce.chem.fsu.edu)
4. High-& Low-resolution data collection procedures
5. Low (cryo) temperature data collection procedure
Writing a
tape using DDS3 tape drive (raccoon.chem.fsu.edu)
Extracting
(reading) from tape
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Chapter 1 |
Facility Information & Contact Numbers
This chapter deals
with the Information about the X-Ray Crystallography Facility and the names and
contact numbers of relevant people.
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t |
he
X- Ray Facility (XRF) established in
1993 is located on the fourth floor of, Kasha Laboratory, Institute of
Molecular Biophysics. It occupies ~1200 ft2
of space spread among four different rooms KLB 410, 411, 412, & 413. It is a multi user macro-molecular x-ray
diffraction laboratory equipped with three copper rotating anode generators
(Rigaku H2Rs and Elliott GX-20), one R-Axis IIc image plate (IP) detector and one Mar165 charge-coupled device (CCD) detector. The x-ray generators
are coupled to either Osmic Confocal
The
facility provides the following services:
1. Single crystal (capillary or
loop mounted) x-ray diffraction data collection from proteins, nucleic acids,
viruses and complexes of macromolecules using automated image plate or CCD detector.
2. Macromolecular
crystallographic data collection at temperatures from 80 to 400 K
using gaseous nitrogen stream including cryo data collection using cryo
loops.
3. Low- and high-resolution
data collection using large sample to detector
distances (w/ Helium path) and non-zero 2-theta angles.
4. Preliminary data processing
(indexing, merging and scaling) of single crystal data sets using popular data
processing software.
5.
Fiber
diffraction data collection from fibrous
proteins and viruses using either standalone image plate or x-ray film with
double mirror focusing system.
6.
Two
individual dedicated areas (one for ambient temperature and the other at 4°C)
for setting-up, monitoring, documenting and mounting crystals of
macromolecules.
7.
Facility and hardware
to flash-cool, store and transport macromolecular crystals for synchrotron
beamline data collection.
8.
Co-ordinate
“our” beam-time at SER-CAT at APS by requesting time-slots, provide expertise
in data collection and processing of the samples.
9.
Provide both
archiving and retrieval of archived data to and from diverse media and
platforms.
Clickable layout of X-Ray Facility. Facility Manager’s is Room KLB414.
The
contact for day-to-day activities of the Facility is
More information about the facility can be found in the web pages of the Facility or the Facility Manager.
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icon key ( Contacts : Data Collection @ Tools < Data Archiving Data Processing & References |
Telephone numbers* (updated May 2004):
Thayumanasamy Somasundaram (KLB 414) 644 6448 (Office)
X-Ray Facility (KLB 410) 645-1333
Soma’s Residence (for emergencies only) Inside the Facility
Emergency/Urgency (Police/Fire) 911 /311
* If calling from a campus phone replace 644 by 4 and 645 by 5. To call outside first dial 9 then the 7 digit number
X-Ray Facility's two main generators, Image plate detector system, and CrystalClear processing software were all installed and
tested by Rigaku/Molecular Structure Corporation (Rigaku/MSC), The Woodlands,
Vendor
& Supplier Telephone Number:
Rigaku/MSC USA 800 543 2379/281 363 1033
Mar USA Inc
Haskris 847 956 6420
Oxford Cryosystems 866 OXCRYO8 /781 8435900
Osmic 800 366 1299/248 232 6400
Hampton Research 800 452 3899
A complete list of all the vendors and suppliers can be found in the Standard Operating Procedure file-folder and is periodically updated.
X-Ray Facility purchase orders are handled by Soma with the permission of the Director of the Institute and coordinated with IMB Fiscal Office (Alice G. Connor). The fiscal year starts July 1stof every calendar year and ends with June 30thof the following year. The director of the Institute with the consultation of other faculty members using the facility approves a budget for every year. Purchases, repairs, and services for the facility are allocated from the budget. So far the Facility does not charge any users for the use of Facility.
Several blanket purchase orders are drawn at the beginning of each fiscal year for vendors with whom the Facility deals frequently. Purchases with these vendors can be made simply by calling in the items and providing the vendor with blanket purchase-order number. Individual purchase order number needs to be taken from the Fiscal office for all other vendors and services. The following is the list of vendors with whom the Facility has blanket purchase orders:
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No |
Vendor Information |
Phone |
Material/Service |
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1 |
1-850-644-3429 |
Glassware, liquid nitrogen, helium gas, & miscellaneous |
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2 |
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1-850-575-4137 |
Hardware supplies |
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3 |
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1-800-547-4239 |
Media, computer accessories |
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4 |
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1-949-425-1321 |
Cryo crystallographic supplies |
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Chapter 2 |
Generator Start-up & Data Collection
The following is a standard
operating procedure for powering up the generator. For the detailed procedure please read the x-ray generator manual
kept at Room Number KLB 410A. Contact
Soma (by phone at
http://www.safety.fsu.edu/radbadge_form.html
There are two logbooks: one for the generator and one for data collection. |
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Figure 1.1. Chilled water supply, valves and controls. |
Figure 1.2. Haskris water chiller with dials and flow meters. |
Haskris water chiller should be running before flipping the ‘ON’ handle in the breaker box. Failure to do so will disable the generator. |
There should be one nylon hose each from the Primary and Reserve regulators to the Cylinder Switcher. However, only one white braided hose out of it. |
Failure in any one of the conditions will prevent the generator from starting. |
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Figure 1.7. Vacuum control panel at the back of the generator. |
Figure 1.8. Water-flow and temp sensors. |
· If the OPERATE amber light is not lit it indicates the following: 1) the 12V/110 mA Ready light in the lamp post has burnt out, or 2) the OL-387 lamp has burnt out, or 3) both lamps are burnt out. Replace them first before proceeding.
Maximum load for our generator (w/ 0.3 mm cathode) is 5.4 kW. |
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Figure 1.15a. Shutter Position for R-Axis IP. |
Figure 1.15b. Shutter Position for marCCD. |
· Note: Before opening the shutters please read the manual thoroughly. Once the shutters are opened and if there is inadequate shielding, there is nothing to prevent you from accidentally being exposed to the radiation.
The following is a standard operating procedure intended to be an introduction for powering down the generator. For the detailed procedure please read the x-ray generator manual kept in KLB410A. In addition, get trained by Soma before actually using the instrument.
·
The red light at the light tower (aka Lamp Post; Figure 1.14) indicates that x-rays are
being produced and the amber lights indicate which x-ray port is open for your
experiment.
·
Carry out your experiment(s).
·
Close the shutters after your experiment is finished. If you are using R-Axis the shutters will be closed when the data
collection ends in normal mode.
·
Reduce the TUBE VOLTAGE and the TUBE CURRENT in steps. They can be brought down rather quickly
unlike the power-up procedure:
·
After reaching 20 kV and 10 mA, press the white X-RAY 'OFF' button (Figure 1.11).
·
Press the red 'OFF' button in the X-RAY panel. Wait for five (5) minutes.
·
Press the red STOP button in the VACUUM panel (Figure 1.10).
·
Wait for 15 minutes for the generator and the target to cool down.
·
Flip the handle to OFF position in the circuit breaker on the wall (Figure 1.3).
·
Turn the handle back to ‘OFF’ position on Helium Control Box (Figure 1.6)
·
Close the inlet and outlet valves to the chilled water.
·
Switch ‘OFF’ the Helium Cylinder Switcher (Figure 1.5)
·
Close the helium cylinder valve.
·
Switch OFF the water chiller.
·
Enter the final value of hour meter and time of the day in the
generator logbook.
·
If you have encountered any problems or difficulties during data
collection please report it to Soma.
This now concludes the
section describing how to power-up and power-down the generator for data
collection.
Regular data collection consists of several simple but important steps that depend upon whether it is: 1) low resolution or high resolution data collection, 2) helium-filled beam paths, or 3) non-zero 2-theta, etc. If a user wants to collect room temperature data for a known crystal (i.e., the user is fairly familiar with the space group and cell constants) the following procedure is followed:
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CAUTION X-RAY
GENERATORS PRODUCE COLLIMATED IONIZING RADIATION. PROPER PROCEDURES NEED TO BE FOLLOWED TO
AVOID SERIOUS INJURY AND PHYSICAL HARM. EVERYONE
USING THE X-RAY FACILITY IS REQUIRED TO TAKE RADIATION SAFETY COURSE
OFFERED BY RADIATION SAFETY OFFICE BEFORE USING THE INSTRUMENT. |
Regular Data Collection
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· The Facility has an Image plate detector and a Charge-coupled device (CCD) detector. The user contacts Soma via telephone, e-mail or in person and requests time for the data collection on a specific or either of the detectors.
· For most of the samples, a tentative date and time is assigned for the data collection. For fragile or one of a kind sample, a particular date and time can be assigned. Users can look at the current and upcoming schedules at the following XRF URL:
http://www.sb.fsu.edu/~soma/XraySchedules/schfrmset.html
· A day prior to the scheduled time, user mounts the crystal in a glass or a quartz capillary (0.3-1.0 mm diameter). The exact placement of the crystal from at least one end of the capillary should be between 12 and 18 mm.
· On the day of the data collection, capillary containing the crystal is mounted onto a goniometer at the x-ray laboratory and the crystal position adjusted to match the beam center.
· Based on the prior experience with a similar crystal, the sample-Image Plate (IP) or CCD distance is set. In case of IP several 2-theta angles can also be set. If needed a helium-filled beam path or additional beam-stop are introduced (it usually takes additional an hour for this modifications).
· At the computer (Windows NT anaconda.sb.fsu.edu for IP and Linux, spruce.sb.fsu.edu for CCD), the user logs in with their username and password. If it is the first time data collection, username and password can be obtained from Soma.
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· Log in with username and password to the Windows NT machine anaconda.sb.fsu.edu. Launch CrystalClear by clicking the icon (see sidebar) or use the run command with the following argument: C:\Program files\Rigaku MSC\CrystalClear\CrystalClear.exe
· Log in to Crystal Clear program with username and password.
Typical user directory name:TSMay00-1M, MSCDec99-10R, SBJul01-3M, etc., |
· You will be put in a data directory (either D:\data\username or E:\data\username. Create a sample directory preferably with the following name convention.: AAJun01-1R (two or three user initials in caps, three letter abbreviation of month with first letter cap, two digit year, a ‘-’, one or two digit experiment number, and finally R for R-Axis or M for MarCCD.
· Start the data collection. More detailed information about the data collection is provided in Chapter 3.
· You need to specify the starting phi, delta phi, and ending phi angles. Exposure time and number of frames are also need to be specified.
· Begin the data collection and wait for exposure time + eight (8) minutes to see the first frame. Confirm that every thing looks okay and allow the data collection to proceed. In case of failure modify one or more of the following: crystal, sample-IP distance, beam-stop, helium flow, phi rotation, delta phi, or exposure time.
· Log in to the Linux machine spruce.sb.fsu.edu with username marccd and password will be provided by Soma. Go to the directories (either /d1/ or /d2/ in spruce.sb.fsu.edu).
· Create a user directory preferably with the following name convention: SIBMar01-1M (two or three user initials in caps, three letter abbreviation of month with first letter cap, two digit year, a ‘-’, one or two digit experiment number, and finally R for R-Axis or M for MarCCD.
· If you prefer you can create sub-directories called Data, Denzo, Mosflm, etc. From the Data directory launch marccd program by issuing marccd command (do NOT put it in background).
· Specify starting, ending, and delta phi., sample-CCD distance, and time of exposure.
· Begin the data collection and wait for the first frame to appear. Unlike IP detector, it takes only three seconds for the data to be read. Confirm that every thing is okay. If not adjust one of the following: crystal, phi values, exposure time, or distance.
· More detailed data collection information will be given in Chapter 3.
Special
Procedure
High- or low-resolution data collection is special a procedure and therefore, requires additional planning. |
For crystals that require high-resolution data collection (i.e., over and above achievable with smallest sample-IP distance of 65 mm; 1. 7 Å at the edges or CCD distance of 35 mm and 1.35 Å at the edges or crystals with larger than 100 Å cell edges), 2-theta stage has to be rotated with respect to the phi axis. The extent of 2-theta stage rotation depends upon the level of high-resolution required (consult separate tables, kept at the XRF, for IP and CCD detectors). When the 2-theta stage is rotated the direct beam strikes the detector at a location different from the physical center of the detector. For IP detector rotation of 30° is achievable for our 2-theta stage. For CCD, limited 2-theta off-sets are available by physically removing the aluminum blocks on which the CCD itself sits. Tables available in the X-Ray Facility consisting of the three related parameters namely: 2-theta swing, sample-detector distance, and the highest achievable resolution (for Copper Ka radiation) can be consulted for the correct 2-theta swing angle for both IP and CCD.
However, the increased resolution comes at the cost of decreased amount of total coverage of the diffraction data because the detector is now off-centered. This means the data needs to be collected for larger phi angles. Larger off-centered detector may require the use of beam-stop mounted on the collimator rather than the one mounted in front of the detector. Collimator mounted beam-stop casts a larger shadow on the detector than the beam-stop mounted in front of the detector. High-resolution data collection may also require the use of a low-temperature device (cryo crystallography) discussed later in this Chapter.
During a low-resolution data collection, the sample-IP distance is increased to a high value, say 400.00 mm. Due to the increased distance x-ray beam traverses between sample and IP there is increased air (non-Bragg) scatter. This scatter produces a higher background in the images. Therefore, it is essential to introduce the flexible helium tunnel equipped with a beryllium window between the sample and the detector (currently supported only on IP) to reduce the air scatter. However, addition of helium tunnel introduces four additional reflecting surfaces (two beryllium and two Mylar) for x-rays while reducing the air scatter. Each interface reflects approximately four (4%) of the intensity. It has been estimated that replacing one centimeter of air by helium decreases the air scatter by one percent. The beneficial effect of helium tunnel, therefore, overcomes the intensity reduction due to reflection for sample-IP distances ≥ 150.0 mm. Low-resolution data collection may also require a new and bigger beam-stop to capture the diverging straight beam and increased exposure time.
Pictures of Cryo accessoriesPictures of Cryo Loop, Cryo Pin and Cryo Cap are shown in Figure 1. |
For low temperature (cryo), data collection we routinely use Oxford CryoSystems Cryo Stream cooler. First the reservoir for the cryo cooler needs to be filled with liquid nitrogen (~ 50 L). Then an appropriate temperature suitable for the crystal (between 95-100°K) is selected. Cryo cooler controller is then programmed to pre-cool to the selected temperature. In consultation with Soma, the user decides upon the height and diameter of the Cryo LoopÔ for his/her crystal. The selected Cryo Loop is glued to a Cryo Pin and the Cryo Pin in turn is glued on to a Cryo Cap. A special magnetic holder is inserted into the goniometer's central hole and tightened. The Cryo Cap Loop is then placed on top of the magnet and the goniometer is adjusted to coincide with the x-ray beam with the center of the loop. Meanwhile, the user serially equilibrates his/her crystal in an appropriate cryo protectant. Then when the pre-set temperature is reached at the cryo cooler, the user brings in his/her crystal immersed in the cryo protectant to the Facility to be mounted using the Cryo Loop.
· User contacts Soma via telephone, e-mail or in person and fixes a tentative date and time for the data collection.
· User selects an appropriate Cryo Loop (diameters 0.2-1.0mm range) depending upon the size of the crystal.
· The selected Cryo Loop is attached to a Cryo CapÔ and the mounted on top of a goniometer with a help of a magnet. The center of the loop is adjusted to beam center.
Cryo Data CollectionCryo data collection procedure requires prior planning both by the user and by the Facility. |
· User picks the crystal with the Cryo Loop, temporarily blocks the flow of the cryo stream and very quickly mounts the crystal on the goniometer. Flow of the cryo stream is restored to flash cool the crystal in the loop. The finer adjustment of the well frozen (vitreous ice and NOT crystal ice formation) crystal is quickly performed.
· At the computer, starting phi, delta phi, and ending phi angles are set. Exposure time and number of frames are also set.
· Begin the data collection. Collect the first frame and confirm that every thing is okay. Allow the data collection to proceed.
· After approximately 36 h of data collection, liquid nitrogen reservoir needs to be manually refilled with liquid nitrogen. Cryostream Cooler attached to MarCCD165 has an auto-refill system and therefore there is no need for manual refill as long as there is enough liquid nitrogen in supply tank, the supply tank is connected to the refill system, and the refill system is ON.
· Upon completion of the data collection, bring the temperature to ambient, switch off the cryo cooler, switch off the external dry air supply.
Pictures of some of the cryo
components used are shown below (Courtesy of Hampton Research ):
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CryoCap |
CryoLoop |
Mounted CryoLoop |
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CryoTong |
CrystalWand |
VialClamp |
Figure 5.1 Pictures of cryo accessories
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Chapter 3 |
Data Collection
Details of data collection
In the previous section, the data collection procedure has been outlined and the details are elaborated in this section. Login with username and password (Windows NT default: press Ctrl, Alt and Delete together to get login box) to anaconda.sb.fsu.edu. Double click Crystal Clear icon or use the Run command with the following argument: C:\Program files\Rigaku MSC\Crystal Clear\Crystalclear.exe. The user will see another log in screen with Crystal Clear logo on it (Figure 3.1). Log in again with username and password.
Fig. 3.1. Crystal clear log-in screen.
Crystal Clear program opens with a full screen (see Fig. 3.2). This screen has several sections: 1) toolbar section, 2) task window 3) icon section, 4) flow bar window, 5) messages window, 6) Stop/Abort button, and 7) Info window.
Fig 3.2. Full screen crystal clear window.
Following the full screen window, crystal clear will prompt for a new project and/or new sample name, depending upon whether it is a new project or a new sample (see Fig. 3.3). Provide the project/sample name such a way that they are consistent with
Fig. 3.3. New sample/project wizard
UNIX conventions (we will be using both Windows NT and UNIX operating systems). This means no spaces, no special characters like ‘#, /, \, *, @, !,?, &’. The program will then ask for a Task with the possible selection includes: Screen Collect and Process, Collect and Process, Process, etc. Depending upon the nature of data collection select the appropriate task, for example, if you want only collect the data, select Collect. But if you wish to first screen several samples before collection, select Screen Collect and Process.
Fig 3.4. Task selection wizard.
Next, the Image Files dialog will open up. In this you will see your default data directory and possibly the correct disk name, for example, D:\data\username \projname\xtalname\images. If this is incorrect, use the Browse button and select the correct directory for the images (see Fig. 3.5). Finally click Finish.
Fig. 3.5. Image directory dialog.
For collecting data using marCCD165 first login to spruce.sb.fsu.edu (Linux machine) with username ‘marccd’ and Soma will provide you with a password.. Change either to /d1 or /d2 directory and create sub-directories (follow the rules of suggested directory names) called Data and Denzo. Change to Data directory and issue command marccd to start the data collection GUI (see Figure 3.6). But DON’T run marccd in the background.
Figure 3.6 MarCCD 165 data collection GUI. Legend: 1=File Menu, 2=Status Menu, 3=File Name, 4=Data, 5=Magnified Data, 6=Cursor Information, and 7= Goniometer Information.
Now the user has to decide either to collect a single frame (more suitable for screening the sample) or a data set. If one desires to screen samples before the actual data collection, go to Acquire menu and select sub menu Single Frame (Acquire>Single Frame). A small window pops open on top of the main GUI asking for details of the single frame data collection (see Figure 3.7).
Figure 3.7 Single Frame CCD data collection GUI. Legend: 1=Goniometer Information, 2=Data Collection Information, 3=Start & Stop Commands, 4= Directory Information, 5=Auto-Save Function, and 6=File Name.
In the Acquire Single Frame sub-menu user specifies Phi, Distance (sample-CCD) in mm, Time (Exposure) in seconds, Scan (delta phi) in degrees and Clicks the Start button to start the exposure and click the Dismiss button to clear the sub menu GUI. One important difference between data collection using CCD and IP is that in the case of CCD the user has to physically open the shutter switch. During IP data collection the instrument opens the shutter automatically. This difference is shown in Figure 3.8a (marCCD) and Figure 3.8b (R-Axis IP).
|
Fig 3.8a The Right Port
shutter is shown in OPEN position for normal operation of marCCD |
Fig 3.8bThe |
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CAUTION THIS MEANS
THAT THERE IS A SIGNIFICANT DIFFERENCE IN THE X-RAY SHUTTER POSITIONS BETWEEN
NORMAL marCCD AND R-Axis IP OPERATIONS. EVERYONE
USING THESE INSTRUMENTS SHOULD BE WELL AWARE OF THIS TO AVOID ACCIDENTAL
EXPOSURE TO X-RAYS. |
Therefore, during the actual x-ray exposure the x-ray shutter in the marCCD base will open to allow the x-rays to fall on the sample. An overall and close-up views of this shutter is shown in Figure 3.9a & b. Once again users should be aware of the difference between marCCD and R-Axis IP operation, as these instruments were manufactured by two different vendors.
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Figure 3.9a |
Figure 3.9b Close-up view
mar shutter red light ON for normal x-ray exposure |
If the exposure is going to last more than 120 seconds, it is advisable to select Multi-Read in the GUI. If selected, Multi-Read = 2 (radio button turned orange), will split the Time (Exposure) into two halves and read the CCD two times, thus eliminating any zingers. Zingers are eliminated by comparing the first half to the second and removing any differences between the two, assuming zingers are random events. During data collection top window will be updated every ten seconds or so with the following details 1) name of current protocol, 2) time left in current exposure, 3) Intensity value 4) Shutter status, 5) Temperature of CCD, 6) Pressure of CCD and 7) Status of cooler (Figure 3.10). After the exposure time is over, CCD takes about 3 seconds to complete the data reading and displays it in the main window (Figure 3.11).
Figure 3.10 marCCD status window
After screening the samples for the best one, the user can then start with their regular data collection by selecting Acquire>Dataset sub menu. A new data-set window will open up (Figure 3.12). The user can complete the required information and start the data collection. Consult the marCCD manual for further details.
Figure 3.11 Image of the data collected using marCCD165. Central white spot is from the lead beam-stop
Figure 3.12 Data set window. See manual for more details. Legend: 1=File Info., 2=Comments, 3=Directory Info., 4=Multi-read, 5=Data Collection Dialog, 6=Auto-Check Button, and 7=Start & Stop Function.
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Chapter 4 |
Archiving data
Long-term storage and retrieval of data in/out of magnetic tapes and recordable CDs (CD-R)
Tape Back-up
Archiving data involves both writing as well extracting the data to and from 4mm tape, 8mm tape or a CD-R. |
Compressed capacity quoted assumes 1:2 compression. |
Archiving and long-term storage of the data is an essential component of any successful data collection procedure. The responsibility lies heavily on the users to ensure that the data is archived and accessible to them whenever they need it. Upon completion of an experiment, the data will remain in the hard disk for two weeks. During this period the user should back-up data by writing to DDS-4 or DDS-3 tapes (sometimes wrongly referred to as DAT tapes). Alternatively the user can write the data to a CD-R or CD-RW (maximum capacity ~700 MB/CD). Another possible but not a recommended option is to copy the data to another hard disk via the network. The Facility has DDS-4 drives connected to anaconda and spruce via SCSI cables (DDS4 media capacity for native/compressed format is 20/40 Gb, for a 155 m tape), DDS-3 tape drive connected to raccoon via SCSI cables (DDS3 media native/compressed capacity is 12/24 Gb, for a 125 m tape). One copy of all the data is kept in the Facility either in DDS-3 or DDS-4 format tapes before it is removed from the hard disk. Due to the larger capacity of DDS-4 and -3 tapes and due to the unreliability of our older 8mm tape-drive, beginning April 2000 the Facility’s archives will be kept only in DDS-4 or -3 formats (data prior to year 2000 are archived in 8mm or DDS formats). These archived tapes are meant for emergencies and never for regular retrieval of user's data.
Our Certance DDS-4 & -3 drives (formerly Seagate) are backward compatible and therefore can read and write tapes with DDS, DDS-2 and DDS-3 specifications (look for logos shown below).
![]()
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Figure 4.1 Logos identifying DDS, DDS2, and DDS3 tape media.
Log in with username and password. If you don’t have username and password ask Soma for one. Change to a directory one level above your data directory. This will usually be either /spruce/d1/ or /spruce/d2 or /raccoon/d3/ or /raccoon/d4. Confirm the size of the directory you are planning to archive (total number bytes of all data) using the command du -ks dir_name. Decide on whether to archive the data in a DDS4 or DDS3 tape ensuring that the amount of data being archived is not larger than the capacity of the tape (uncompressed capacity for DDS4 and DDS3 are 20 and 12 GB, respectively). Insert a fresh tape into the appropriate tape drive with the tape's write-protection tab moved out of way. For DDS4 and DDS3 tapes a closed-tab allows writing.
Issue the tar command in the generic format tar -cvf /dev/st0 directory_name and this will start archiving the directory and all its sub-directories.
tar -cvf /dev/st0 dir_name/ &
Shown below is a typical session for DDS4 tape writing and reading (commands that you issue are shown in italic courier font, the computer response is shown in Arial Narrow font and comments in regular Times New Roman font).
We will first consider writing to DDS3 tape in this section. |
>pwd ¿ [Check the directory]
raccoon>/d3/Ip/soma
>ls -ltFa ¿ [Checking the list of sub directories]
total 48
drwxr-xr-x 5 soma
users 4096 Sep 18 16:17
DDSRestore/
drwxrwxr-x 16 xray
users 4096 Sep 18 10:49 ../
drwxr-xr-x 12 soma
users 4096 Sep 18 10:46 ./
drwxr-xr-x 9 soma
users 4096 Aug 31 11:58
E225QTsac/
drwxr-xr-x 4 soma
users 4096 Aug 25 15:50
ApoAkAug01/
drwxr-xr-x 2 soma
users 4096 Jun 20 15:34
LysDenzoHDisk/
>du -ks E225QTsac/ ¿ [Checking the size of the directory to be archived]
1298648 E225QTsac / [~1.2 Gigabytes, a small directory]
>mt -f /dev/st0 status ¿ [Checking status of tape and drive]
SCSI 2 tape
drive:
File number=0,
block number=0, partition=0.
Tape block size
512 bytes. Density code 0x25 (DDS-3).
Soft error count
since last status=0
General status
bits on (41010000):
BOT ONLINE IM_REP_EN Controller: SCSI
>tar -cvf /dev/st0
E225QTsac/ & ¿
[1] 3470
or
>tar -cvf /dev/st0 E225QTsac/ | & tee
~/Tapes/dds3-01.list & ¿
[Writing
tape as well as listing it into a file simultaneously]
Writing to DDS4 drive is exactly the same except for their higher capacity. |
[1] 3478 3479
DDS4 drives are backward compatible with DDS3 DDS2 and DDS formats. Similarly DDS3 drives are backward compatible with DDS2 and DDS formats. Further information about writing to tape can be found in the Linux/UNIX man pages, Facility web manual pages or by consulting with people more familiar with the operating system.
http://www.sb.fsu.edu/~xray/Manuals/misc_man.html
Login with username and password. From the Start menu select Programs> Administrative Tools (Common)>Backup (see Figure 4.2). This will open up Windows NT back up GUI (see Figure 4.3a). Now select one of the disks shown on the GUI (in the example shown, drive D: has been selected). Then click Backup on the menu button. Another window pops open (Figure 4.3a) and in this window specify what exactly needs to be backed up (archived). There are several options, e.g., does the backup is replacing (new) or appending (add to old), does one need full details, or less detail, does one need daily, differential, incremental or full backup. After selecting all these options, click on OK. This starts the back-up process. More details can be found in the XRF Web page link to the Manuals page:
http://www.sb.fsu.edu/~xray/Manuals/misc_man.html
Alternatively Windows NT Back-up book or manual can be consulted for in-depth understanding of the complete procedure of back-up and restoring.

Figure 4.2 Invoking Windows NT backup program (DDS4 drive) on anaconda.sb.fsu.edu
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|
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Figure 4.3 Window NT Backup GUI
In this section, we will discuss extraction of data from tape. |
In this section we will look at the procedure to extract
the archived data back to hard disk. We
can extract either all the contents of the directory or only part of the
tape. The latter procedure is probably
used most of the time since tapes usually contain more than one data set. However, in order to extract a particular
directory it is essential to know the exact path name of that directory while
the data was archived. It is, therefore,
recommended that the user makes the listing of the contents of the tape as and
when they are archiving their data (see the special command described in the
earlier section, look for the following sign
in the left hand margin)
>pwd ¿ [Checking the present
working directory]
/d3/Ccd/soma
>df -k . ¿ [Checking the amount of
available free-space in current directory {.}]
Filesystem 1k-blocks Used Available Use% Mounted on
/dev/sda1 17639220 8004440
8738760 48% /d3
>mkdir new_dir
¿ [Making a new directory for
extraction]
>cd new_dir
¿ [Moving to the new
directory]
>tar-xvf /dev/st0 & ¿
[Extract all the contents of tape]
>tar
-xvf /dev/st0 | & tee extract.list & ¿
[Extracting
and simultaneously writing the lists of extracted files into a file. "|" for pipe, first
"&" for standard output, "tee" for one input to two
output redirect, and the final "&" to put the job in background]
or
>tar -xvRf /dev/st0 a/data/proc/dir_name3
& ¿
[Extracting
only contents of one directory {dir_name3}.
Note here, there is no leading or succeeding slash in the directory
designation].
The data will now be extracted to the hard drive.
Index
#
ã, i
A
anaconda,
i, 12, 14, 19, 25, 28
Archiving data, i, 25, 26
B
Backup, 28, 29
C
CCD, i, 13, 14, 15, 22, 23
Charge-coupled device, 13
chilled water, 8
circuit breaker, 8
cryo, i, 2, 4, 16, 17, 18
CryoCap, 18
CryoLoop, 16, 17, 18
Cryostream, 17
CryoVial, 18
CryoWand, 18
Crystal Clear, 14, 19, 20
CrystalClear, 4, 14
D
data collection, i, 2, 7, 12, 13, 14, 15, 16, 17, 19, 21, 22, 23, 25
DDS4, 25, 26, 27, 28
Denzo, 15, 22
E
Emergency, 4
Extracting data, i, 29
F
Facility Information, 1
filament, 11
Florida State
University, 0, i
G
Generator shutdown, i, 12
Generator start-up, i, 7
H
Hampton Research, 4, 5, 17
Haskris, 4, 5, 7, 8
helium, 8
I
Image plate, 4, 13
Institute of
Molecular Biophysics, 0, i
IP, i, 14, 15, 16, 19
J
John Beidler, 4
L
Linux/UNIX, 26, 27
load capacity, 11
M
Mar/USA Inc, 4
MarCCD, 14, 15, 22
marCCD165, 4, 22, 23
Mike Zawrotny, 4
Mosflm, 1, 15
O
OPERATE, 10
Osmic, 1, 4, 5, 8, 9, 12
Oxford Cryosystems, 4, 5
R
R-Axis, 1, 8, 12, 14, 15
Rigaku/MSC, 4
S
shutter, 11
Soma, 3, 5, 7, 12, 13, 14, 15, 16, 17, 22, 26
spruce, i, 14, 15, 22, 25, 26
STOP button, 12
T
Table of
Contents, i
Telephone numbers, 4
Thayumanasamy Somasundaram, 4
TMP, 9
V
Vacuum, 7, 9, 10, 11
W
Windows NT, i, 14, 19, 21, 27, 28
X
X-RaY FACILITY, 13
XRF
Floor plan, 3
XRF URL, 13
1, 1