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[B]NMR Sample Preparation[/B][B] from NMR2.0 Wiki 
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[B][URL="http://www.bionmr.com/forum/redirector.php?url=http%3A%2F%2Fwww.nmr2.buffalo.edu%2Fnesg.wiki%2FNMR_Sample_Preparation"]http://www.nmr2.buffalo.edu/nesg.wiki/NMR_Sample_Preparation[/URL]
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originally posted by  Main.Gaohua.Liu (11 Feb 2007)         
  

<!-- start content -->             <table style="width: 76px; height: 63px;" id="toc" class="toc" summary="Contents"><tbody><tr><td>[B]Contents[/B]

 </td></tr></tbody></table><script type="text/javascript"> if (window.showTocToggle) { var tocShowText = "show"; var tocHideText = "hide"; showTocToggle(); } </script> [B]  [B]Sample Transfer into NMR Tubes[/B]  [/B]

 Typically, three kinds of NMR tubes are used: regular 5 mm NMR tubes,  Shigemi tubes and capillary tubes. Each kind of tube has its own  special sample preparation procedure.  
 [B]  [B]Regular and Shigemi Tubes[/B]  [/B]

 Regular NMR tubes:  
 
[LIST]
[*]Pros
[LIST]
[*]Easy to transfer or titrate sample.
[*]Low price.
[*]Durable.
[*]Can be used with any spectrometer brand.
[/LIST]
 
[*]Cons
[LIST]
[*]Requires large sample volumes - 0.4 to 0.6 ml.
[*]Suboptimal shimming, consequently, water suppression and sensitivity are poor (and smaller the volume, worse is the effect).
[*]Sample is subject to air oxidation.
[/LIST]
 
[/LIST]
 Shigemi NMR tubes:  
 
[LIST]
[*]Pros
[LIST]
[*]Ideal for small sample volumes: 0.2 to 0.3 ml
[*]Optimal shimming and water suppression
[*]Better sample stability due to reduced air oxidation
[/LIST]
 
[*]Cons
[LIST]
[*]Complicated transfer and handling.
[*]High price.
[*]Very brittle - easy to break.
[*]Different tube types for different spectrometer brands.
[/LIST]
 
[/LIST]
 In general, it is preferable to use Shigemi tubes for [U-15N,  13C]-labeled samples. For [U-15N, 5%-13C]-labeled samples, regular tubes  are also fine, since these samples are used to record in general the  13C-HSQC spectrum of the methyl region, where water suppression is not  an issue.  


 [B]  [B]Protocol to transfer sample in a regular tube:[/B]  [/B]

 Fig.1 Sample in regular NMR tubes  
[URL="http://www.bionmr.com/forum/redirector.php?url=http%3A%2F%2Fwww.nmr2.buffalo.edu%2Fnesg.wiki%2FFile%3ASample1.jpg"][IMG]http://www.nmr2.buffalo.edu/enter/NMRWiki/images/d/d0/Sample1.jpg[/IMG][/URL]  
 
[LIST=1]
[*]Using a long-tipped Pasteur pipette transfer the sample solution into the NMR tube and cap it.
[*]Spin the tube in the hand centrifuge to collect residual sample  from the walls and collapse air pockets and bubbles, if any. Wrap the  tube in a tissue for padding before inserting it into a holder of the  centrifuge.
[*]If a part of the sample collected in the cap, transfer it into the tube and spin the sample again.
[*]Wrap a thin strip of Parafilm around the seam between the tube and its cap to prevent the sample from drying out.
[*]Put a label on the tube.
[/LIST]
 [B]  [B]Protocol to transfer sample in a Shigemi tubes:[/B]  [/B]

 Fig.2 Sample in Shigemi tubes  
[URL="http://www.bionmr.com/forum/redirector.php?url=http%3A%2F%2Fwww.nmr2.buffalo.edu%2Fnesg.wiki%2FFile%3ASample2.jpg"][IMG]http://www.nmr2.buffalo.edu/enter/NMRWiki/images/2/22/Sample2.jpg[/IMG][/URL] 

 The Shigemi tube is composed of two parts: the outer tube  and the insert (also called plunger). The insert is made of a special  type of glass with magnetic susceptibility matching to that of the  solvent (H2O for protein NMR). The matching magnetic susceptibility  removes the edge effect at the interface of the sample and the glass,  thereby improving the shimming. The whole set is expensive (~ $80 per  set) and the glass type is more brittle as compared to the regular  tubes. Extra care should therefore be taken while handling Shigemi  tubes.  

  
 
[LIST=1]
[*]Place the sample at the bottom of the tube and cap the tube.
[*]Spin it in the hand centrifuge to collect residual sample from  the walls and collapse the air pockets and bubbles, if any. Wrap the  tube in a tissue for padding before inserting it into a holder of the  centrifuge.
[*]If a part of the sample collected in the cap, transfer it into the tube and spin the sample again.
[*]Slowly push the insert down the tube to drive the air out.
[*]At this point, it is common to get bubbles under the insert. To  get rid of them, hold the tube at an angle (and maybe knock on it a few  times) - the bubbles should then settle at the interface between the  insert bottom and the tube wall. Push forward quickly, but gently, and  simultaneously rotate the insert.
[*]If you have a lot of bubbles (or foam) in the reservoir then  let the sample stand still for some time. After a while the bubbles will  rise on their own. Keep the inset in place by wrapping a thin strip of  Parafilm around the tube rim.
[*]Pull the insert out without letting any air back in. Make sure  that at least 2-3 mm of solution covers the insert, otherwise air may  get into the active volume due to evaporation.
[*]Repeat steps 5 - 7. if necessary.
[*]Wrap a thin strip of Parafilm around the tube rim. This should  keep the insert in place as well as prevent the sample from drying out.
[*]Label the tube.
[/LIST]
 [B]Additional notes[/B]  
 
[LIST]
[*]Rotate the insert when moving it in or out to reduce the resistance.
[*]Be careful not to drive the insert too far, especially when  pushing air bubbles out. The neck of the insert forms a reservoir in the  tube, but once it is full the sample will leak out.
[*]When immersed in liquid, the insert may easily slide under it  own gravity, especially in thin-walled Shigemi tubes. Therefore, always  fix the insert with Parafilm when leaving the sample unattended.
[*]It is important to push air bubbles out. Even the tiniest  bubbles can lead to broad lineshapes and poor water suppression - and  that is exactly what Shigemi tubes are designed to avoid.
[*]Waiting for foamy solution to settle down before pulling up the  insert can be crucial for maximizing the sample height. With certain  viscous solutions, such as phage-based alignment media, the time  required may be as long as several hours.
[/LIST]
 [B]  Maximum Volume  [/B]

 Shigemi tubes for Varian instruments (BMS-005TV) have bottom length  of 15-16 mm, leaving 16 mm as the maximal sample depth. This corresponds  to 260 ul at 4.52 mm inner diameter. You still need to have some liquid  filling part of the reservoir, meaning that you probably have to put  280-300 ul into the tube.  
It is possible to use Bruker shigemi tubes with bottom length of 8  mm in Varian spectrometers. In this case max sample depth would be 24  mm, corresponding to 385 ul. 
 [B]  Capillary Tubes  [/B]

 We use 1.0mm and 1.7mm O.D. tubes from Wilmad. The capillary action  (with a little help) is always sufficient to draw the solution into the  tube. Normally, aliquot ~30uL of solution into a small Eppendorf tube,  dip the capillary in, and tip or invert the whole setup if the solution  does not completely go into the capillary. If needed, you can apply some  suction from a syringe or pipette or even 'inject' the solution into  the capillary with a syringe and very thin needle although these methods  have a higher risk of squirting your solution onto the bench.  
When sealing the tubes, first start with a good length of  capillary tube (almost as long as the NMR tube) and put sample solution  in it. Then tip the capillary until the solution moves to the middle of  the tube. Now it is safe to seal the end of the tube in a Bunsen burner  flame -- place only the very tip of the tube into the flame. To avoid  the possibility of the protein heat-denaturing while sealing in case of  insufficient space at the end of tube, wrapping the tube with some form  of a 'heat-sink' (like a wet towel placed in a freezer) can be tried.  After sealing one end of the tube, centrifuge the whole set-up (place  sealed end into the centrifuge) by using a small hand-operated  centrifuge for a few seconds to spin down the solution into the sealed  end of the capillary tube. Seal the other end of the tube. As the second  end begins to seal, essentially a closed container is heated. Normally,  bubbles will generate on one end of the tube.  
Some tips for handling capillary tubes and lowering the sample temperature:  
 
[LIST=1]
[*]Don't use capillaries that have been broken on both ends (i.e.,  keep at least one machined end of glass to prevent particles of glass  getting into your solution)
[*]Carefully clean and dry all of the capillaries
[*]Try to keep the tubes perfectly parallel to the magnetic field  by using empty tubes or small pieces of paper wrapped around the top of  the capillary tube to keep everything aligned and motionless in the NMR  tube
[*]Try a few times with H2O/D2O and see how it goes
[*]Before you start, centrifuge the solution at ~14000g for ~30minutes
[*]Use a 1D (no water suppression) and array the temp from -5C to  -20C in -0.1C steps to monitor the cooling. (if one out of ten  capillaries freeze, then a decrease in the intensity of the water line  could be observed)
[*]Don't spin the sample or bump the spectrometer during the cooling progress.
[/LIST]
 
  
 [B]  Short-term and Long-term NMR Sample Storage  [/B]

 All NMR samples should be labeled and stored at 4C or -20C. The label  should include the sample name and concentration, all buffer  components, percentage of H2O:D2O, initials of the preparer and the date  prepared. This should be neatly printed of prepared with a word  processing program. You may also consider a code that is cross  referenced to your lab journal giving more detailed information about  the sample preparation and the sample conditions.  
The optimal method for short-term sample storage, provided the  sample is stable and sodium azide is present, is to simply keep them at  4C. There are plenty of 10 mm tube racks in the refrigerator. For  valuable samples you should place the NMR tubes inside a second  container, e.g., a 10mm capped NMR tube or a homemade container that  will serve to catch any spilled sample in the event of glass breakage.  This doubly protected NMR sample tube should then be placed in a 10 mm  rack.  
The optimal method for long-term sample storage, provided they  are stable upon freezing, is to transfer the solution to a 1.5 mL  plastic Eppendorf tube and then freeze at -20C. The sample can also be  lyophilized at this stage. Lyophilized protein (r.t. or -20C) is  probably the best condition to store biological sample for extended  periods of time.  
Precautions: DO NOT freeze samples directly in the glass NMR  tubes, particularly in expensive Shigemi tubes. The risk of glass  breakage and sample loss is high. If you need to freeze an NMR sample  directly in the tube, then the following precautions must be taken: The  liquid should be spread uniformly on the glass surface prior to freezing  in order to prevent breaking of the thin glass walls; The NMR tube  containing a frozen sample should be placed in a clean container, e.g., a  10 mm capped NMR tube or a homemade container that will serve to catch  any spilled sample in the event of glass breakage; The sample must be  stored in a 10 mm rack provided for this purpose.  


 -- Main.Gaohua.Liu - 11 Feb 2007

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