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=== This Page is Currently Under Construction August 18th 2011===
=== Brief Description  ===
=== Brief Description  ===


NH RDC are easily acquired and for the purpose of protein structure validation and refinement and the data can be collected on samples labeled only with <sup>15</sup>N. Obtaining RDC in two different alignment media greatly improve the quality of refinement and can aid in dimer structure determination; 500ul of a 0.5-0.6mM sample is usually sufficient for this purpose.
<sup>1</sup>H-<sup>15</sup>N residual dipolar couplings (RDCs) are easily acquired for the purpose of protein structure validation and refinement. The data can be collected on samples labeled only with <sup>15</sup>N. Obtaining RDCs in two different alignment media greatly improve the quality of refinement and can aid in dimer structure determination; 500µl of a 0.5-1mM sample is usually sufficient for this purpose.  


=== Data Acquisition to RDC Calculation  ===
=== Data Acquisition and RDC Calculation  ===


Detail description on data acquisition
Refer to the linked pages for detailed descriptions of the [[Jmodulation Experiment RDC]] and [[HSQCTROSY RDC Measurement]] and their respective RDC calculation methods.<br>


=== Alignment Media Preparation  ===
=== Alignment Media Preparation  ===


==== Isotropic Sample Measurement ====
==== Isotropic Sample  ====


The first sample to be observed is an isotropic sample. Dilute one half of the sample by a factor of two as this will give a reference at the concentration of most aligned samples. This can be important in cases of weak dimers. Measure the pH as this will be useful in selecting media later.  
The first sample to be observed is an isotropic sample. You may want to dilute the isotropic sample by one third (to 75% of its original concentration) to match the concentration of most aligned samples. In the case of a weak dimer, this may be important.<br>


==== PEG Biclle ====
==== PEG Bicelle ====


Alignment of the protein sample in PEG(C<sub>12</sub>E<sub>5</sub>/hexanol). This is used as a first alignement media because it produced primarily steric alignment (useful in dimer geometry predictions), the success rate is high, and it can be doped with other charged detergents to give a second alignment media .  
Alignment of the protein sample in PEG(C<sub>12</sub>E<sub>5</sub>/hexanol) is used as a first alignment media because it produces primarily steric alignment (useful in dimer geometry predictions), the success rate is high, and it can be doped with other charged detergents to give a second alignment media .  


Chemical used for this preparation:  
Chemicals used for this preparation:  


:'''Sigma Aldrich 76437''', Pentaethylene glycol monododecyl ether (C<sub>12</sub>E<sub>5</sub> PEG)  
:'''Sigma Aldrich 76437''', Pentaethylene glycol monododecyl ether (C<sub>12</sub>E<sub>5</sub> PEG)  
:'''Sigma Aldrich H13303''', Hexanol  
:'''Sigma Aldrich H13303''', Hexanol  
:'''Sigma Aldrich 855820''', Cetyltrimethylammonium bromide (CTAB)  
:'''Sigma Aldrich 855820''', Cetyltrimethylammonium bromide (CTAB)  
:'''Sigma Aldrich O4003''', Sodium octyl sulfate (SOS)
:'''Sigma Aldrich O4003''', Sodium octyl sulfate (SOS)
:'''Sigma Aldrich 436143''', Sodium dodecyl sulfate (SDS)


The preparation procedure of 16% PEG stock solutionis as follows:  
The preparation procedure is as follows:  


*Mix 50ul of C<sub>12</sub>E<sub>5</sub> (pentaethylene glycol monododecyl ether) with 200ul of buffer and 50ul of D<sub>2</sub>O by vortexing.  
*Prepare the 16% PEG stock solution by first mixing 50µl of C<sub>12</sub>E<sub>5</sub> (pentaethylene glycol monododecyl ether) with 200µl of buffer and 50µl of D<sub>2</sub>O by vortexing.<ref> Ruckert M and Otting G (2000), JACS, 122, 7793-7797</ref>
*Add approx 16ul of hexanol, in aliquots of 2ul with vortexing after each addition. The solution will go from clear to milky, then to translucent and viscous with lots of bubbles. Continue to add hexanol until the solution goes clear again.  
*Add approximately 16µl of hexanol to the stock solution, in aliquots of 2µl with vortexing after each addition. The solution will go from clear to milky, then to translucent and viscous with lots of bubbles. Continue to add hexanol until the solution goes clear again. If it becomes milky/turbid again, you have gone past the nematic phase.  
*Sample Content:
*Sample Content (for 220 µL sample):


::155 uL of Protein  
::145 µL of Protein stock solution<br>
::55 uL of 16% PEG stock solution  
::55 µL of 16% PEG stock solution  
::20 uL of D<sub>2</sub>O  
::20 µL of D<sub>2</sub>O  
:::Final PEG concentration is 4.2%.
:::Final PEG concentration is 4.2%.


*Record the <sup>2</sup>H splitting by running the s2pul expt with tn=lk (for Varian instrument). The range of the splitting should be around ~+/-20Hz.
*Record the <sup>2</sup>H splitting by running the s2pul expt with tn='lk' (for Varian instruments). The range of the splitting should be around +/-20Hz.
 
*PEG can be doped with either cetyltrimethyl ammonium bromide (CTAB) for positively charged proteins or sodium octyl sulphate (SOS) for negatively charged proteins. Charging the medium to be like the protein prevents association and gives higher resolution spectra. A suitable ratio of PEG:CTAB/SOS is ~30:1.
 
==== Pf1 Phage  ====
 
Preparation of a Pf1 phage alignment sample is fairly straightforward.<ref>Hansen MR, Mueller L, Pardi A (1998), Nat Struct Biol, 5, 1065-1074</ref> The protein sample is diluted by the alignment medium.
 
Chemicals used for this preparation:


==== Doped PEG Biclle  ====
:'''ASLA Biotech P-50-P''', Pf1 phage 50 mg/mL


For the second medium, PEG can be doped with either cetyltrimethyl ammonium bromide (CTAB) for positively charged proteins or sodium octyl sulphate (SOS) for negatively charged proteins. Charging the medium to be like the protein prevents association and gives higher resolution spectra. A suitable ratio of PEG:CTAB/SOS is ~30:1. If the protein sample is less than the pI it will be positively charged and if it is more than the pI it will be negatively charged.
The preparation procedure is as follows:  


==== Pf1 Phage  ====
*Start with a protein stock 0.5-1mM and a pf1 phage stock of 50 mg/mL. Prepare a sample of 12.5 mg/mL of phage.
 
*Sample Content (for 220 µL sample):
 
::145 µL of Protein stock solution<br>
::55 µL of Pf1 phage 50 mg/mL stock solution<br>
::20 µL of D<sub>2</sub>O
:::Final phage concentration is 12.5 mg/mL
 
*Record the <sup>2</sup>H splitting by running the s2pul expt with tn='lk' (for Varian instruments). The range of the splitting should be around +/-8-10 Hz.


phage, and poly acrylamide compressed gels Phage: Prepare a solution by adding 120 ul of protein solution (~0.5mM), 80 ul of 50mg/ml of Phage solution (availble from Asla Biotech Ltd) and 20ul of D2O Check the 2H splitting. This is typically 8-12Hz.
==== Polyacrylamide Gel (Compressed and Stretched) ====


==== Polyacrylamide Gel (Compress and Stretch)  ====
The preparation of polyacrylamide gel samples is a two step process. First the gels must be polymerized, equilibrated to the correct pH and cut to the appropriate size before being dried. Second the gels are re-hydrated using the protein stock in the appropriate NMR tube.<br>


Chemicals used in preparing this alignment medium can are:  
Chemicals used for this preparation:  


:'''Bio-Rad 161-0144''', 40%Acrylamide/Bis solution 19:1  
:'''Bio-Rad 161-0144''', 40% Acrylamide/Bis solution 19:1  
:'''Bio-Rad 161-0733''', 10X TBE  
:'''Bio-Rad 161-0733''', 10X TBE  
:'''Bio-Rad 161-0700''', APS  
:'''Bio-Rad 161-0700''', APS  
:'''Bio-Rad 161-0800''', TEMED  
:'''Bio-Rad 161-0800''', TEMED  
:'''Sigma Aldrich M7279-25G''', N,N'-methylenebisacrylamide (BIS)  
:'''Sigma Aldrich M7279''', N,N'-methylenebisacrylamide (BIS)  
:'''Sigma Aldrich 448281''', (3-Acrylamidopropyl)trimethylammonium chloride solution  
:'''Sigma Aldrich 448281''', (3-Acrylamidopropyl)trimethylammonium chloride solution  
:'''Sigma Aldrich 282731''', 2-Acrylamido-2-methyl-1-propanesulfonic acid
:'''Sigma Aldrich 282731''', 2-Acrylamido-2-methyl-1-propanesulfonic acid


===== Compressed Gels can be made Positive, Negative and Neutral =====
Other materials used for this preparation:
 
:'''Wilmad P-4.4965M-6.5135-0-0''', 4.4965mm +/-0.0065mm ID x 6.5135mm +/-0.0065mm. Ground polished and buffed OD. 40mm +/- 0.5mm long. Both ends wet saw cut only.
 
===== Preparation of Dried Acrylamide Gels =====
 
The preparation procedure is as follows:
 
*Prepare the positively and negatively charged 40% 19:1 bis:acrylamide solutions.
*Positively charged stock solution (2mL):
 
::31 mg of N,N'-methylenebisacrylamide (BIS)
::961 µL of (3-acrylamidopropyl)trimethylammonium chloride solution
::1039 µL of H<sub>2</sub>O
 
*Negatively charged stock solution (2mL):
 
::31 mg of N,N'-methylenebisacrylamide (BIS)
::802 mg of 2-acrylamido-2-methyl-1-propanesulfonic acid
::2000 µL of H<sub>2</sub>O
 
{| width="838" cellspacing="1" cellpadding="1" border="1"
|+ Standard formulas for preparing compressed and stretched polyacrylamide gels
|-
| Gel type
| &nbsp;% acrylamide
| &nbsp;% charged
| Vol. 40% charged stock solution (µL)
| Vol. 40% neutral stock solution (µL)
| Vol. 10x TBE (µL)
| Vol. 10% APS (µL)
| Vol. TEMED (µL)
| Vol. per casting tube (µL)
| Type of casting tube
|-
| charged compressed
| 7
| 50
| 43.75
| 43.75
| 400
| 7.5
| 5
| 140
| 2.8 mm ID&nbsp; plastic
|-
| charged stretched
| 5
| 50
| 62.5
| 62.5
| 860
| 10
| 5
| 300
| 3.2 mm ID&nbsp; glass
|-
| neutral stretched
| 5
| 0
| 0
| 125
| 860
| 10
| 5
| 490
| 4.5 mm ID&nbsp; glass
|}
 
Note: The APS solution should be prepared fresh and polymerization will begin as soon as TEMED is added.
 
<br>
 
*Mix stock solutions of neutral and charged 40% acrylamide/bis 19:1 to achieve the desired overall charge ratio.<br>
 
*Dilute the mixtures 10x with TBE buffer (0.9 M TRIS, 0.9 M borate, 0.02 M EDTA, pH 8.2) to a final 7% or 5% concentration for compressed or stretched gels, respectively.
 
*Polymerization is initiated by the addition of ammoniumperoxide sulfate (APS) (0.15% or 0.1% for compressed or stretched, respectively) and tetramethylethylenediamine (TEMED) (0.1% or 0.05% for compressed or stretched, respectively).<br>
 
*Pipet the mixture into the casting tubes carefully, to avoid bubbles, and keep them 1-2 hrs, allowing polymerization to occur.
*Use a 200 µL pipet with a trimmed pipet tip (to avoid hitting the gel) and water to carefully push the compressed gels out of the casting tubes into a 1L Erlenmeyer flask filled with deionized water. For the stretched gels, use a 1000 µL pipet to carefully push the stretched gels out of the casting tubes into prepared racks (no more than 4-5 gels per rack) braced in 2L nalgene beakers filled with deionized water.<br>
 
*Wash the polymerized gels extensively in deionized water (two cycles over a period of 1 day). The gels will increase in size due to electro-osmotic swelling. Use cheesecloth to drain the water from the flask for the compressed gels. Be careful when draining and adding new deionized water not to damage the gels. The racks holding the stretched gels may be moved to a new 2L nalgene beaker with fresh deionized water.<br>
*Equilibrate the polymerized gels to the desired pH (to match the pH of the protein stock) by washing extensively in buffered solution (two cycles over a period of 1 day). The buffer should not contain only the major buffering species and no salts.<br>
*Wash the polymerized gels in deionized water overnight to allow them to swell to full size.
*Select the gels which have no cracks or imperfections and measure the diameter of the fully swollen gels and trim each gel to a length 5.7 times its diameter.
 
*Dry the gels over a 2 day period at room temperature on a teflon pan. If the gels do not dry well (straight, uniform width), but do not break, you can add a few drops of deionized water to slightly rehydrate them and allow them to dry again.<br>
 
===== Preparation of Aligned Compressed Gel Samples<br>  =====
 
*Sample content (compressed gel):
*:1 dried compressed gel equilibrated to the same pH as the protein stock
*:200 µL of Protein stock
*:20 µL of D<sub>2</sub>O<br>
*Measure a height of 12-13 mm for the sample volume in a 5 mm shigemi tube and mark with a sharpie.<br>
*Add one dried compressed gel to the tube, followed by the protein stock and D<sub>2</sub>O.<br>
*Insert the plunger to the marked height and hold in place with parafilm.<br>
*Allow the gel to swell in the fridge for 1 day. Inspect the final sample for cracks before collecting data.<br>
 
===== Preparation of Aligned Stretched Gel Samples =====
 
Chemicals used for this preparation:
 
:'''Sigma Aldrich 440272''', Dichlorodimethylsilane
 
Other materials required for this preparation:
 
:'''Wilmad 528-PP-2.8mm/Stem''', 528-PP NMR tube sealed to a 50mm long stem section (stem dimensions 2.8mm +/-0.025mm ID x wall 0.38mm +/-0.015mm). Overall length, 8 inches. Both ends open'''.'''
 
:'''Wilmad 528-PP-3.6mm/Stem''', 528-PP NMR tube sealed to a 50mm long stem section (stem dimensions 3.6mm +/-0.025mm ID x wall 0.38mm +/-0.015mm). Overall length, 8 inches. Both ends open.
 
:'''Wilmad 528-PP-3.9mm/Stem''', 528-PP NMR tube sealed to a 50mm long stem section (stem dimensions 3.9mm +/-0.025mm ID x wall 0.38mm +/-0.015mm). Overall length, 8 inches. Both ends open.
 
:'''Wilmad 5mm microprobe NMR tube style''', Upper tube 528-PP section 7 inches long sealed to a 50mm long stem section (427-PP). Both ends open.
 
*Sample content (stretched gel):
*:1 dried stretched gel equilibrated to the same pH as the protein stock
*:300 µL of Protein stock
*:20 µL of D<sub>2</sub>O
*Prepare an NMR tube by washing the inside 3 times with dichlorodimethylsilane, then rinse with deionized water and dry.
*Place a dried stretched gel near the top of the 5mm end of the NMR tube and attach a syringe with tubing to the bottom of the tube.
*Carefully pipet in the protein stock and D<sub>2</sub>O allowing the solution's surface tension to hold it in place in the tube.
*Use the syringe to adjust the position of the solution, such that the gel is centered in the column of solution. Cap the NMR tube, and let swell at room temperature 1-2 days. Capping the tube may cause the solution to shift, it's position should be readjusted with the syringe, to keep the gel centered.
*Once the gel is swollen, use the syringe to gently pull the gel down to the lower stem of the tube. Insert a small rubber stopper in the bottom of the tube to prevent the gel from drying. Carefully insert a shigemi plunger in the top of the tube, to the top of the gel or the bottom of the upper stem, whichever is higher.


*Mix stock solutions of 40% acrylamide and N,N'-methylenebisacrylamide in a 19:1 ratio with 40% charged acrylate derivatives containing N,N'-methylenebisacrylamide as desired in a 19:1 ratio.
<br>


*Dilute the mixtures 10x with TBE buffer (0.9 M TRIS, 0.9 M borate, 0.02 M EDTA, pH 8.2) to a final 7% concentration.
=== References  ===


*Polymerization is initiated by the addition of 0.15% ammoniumperoxide sulfate and 1% tetramethylethylenediamine (TEMED).
<references />


*To introduce negative charges, use acrylic acid or 2-acrylamido-2-methyl-1-propanesulfonic acid. Positive charge can be introduced by addition of (3-acrylamidopropyl)-trimethylammonium chloride (APTMAC) or N-(2-acryloamidoethyl) triethylammonium iodide. For neutral gels omit the charged species; for zwitterionic gels use equivalent amounts of acrylic acid and APTMAC. For 50% charged gels use 50% content of the charged specie and 50% acrylamide.
<br>


*Add 130ul of the mixture to plastic tubes with a 3.2 mm inner diameter and keep them overnight allowing polymerization to occur.
<br>


*Wash the polymerized gels extensively in deionized water (three cycles over a period of 2 days). The gels will increase in size due to electro osmotic swelling.
Updated by Hsiau-Wei Lee, 2011


*Dry the gels over a 2 day period at room temperature on a teflon pan.
Updated by Kari Pederson, 2013<br>

Latest revision as of 20:32, 18 December 2013

Brief Description

1H-15N residual dipolar couplings (RDCs) are easily acquired for the purpose of protein structure validation and refinement. The data can be collected on samples labeled only with 15N. Obtaining RDCs in two different alignment media greatly improve the quality of refinement and can aid in dimer structure determination; 500µl of a 0.5-1mM sample is usually sufficient for this purpose.

Data Acquisition and RDC Calculation

Refer to the linked pages for detailed descriptions of the Jmodulation Experiment RDC and HSQCTROSY RDC Measurement and their respective RDC calculation methods.

Alignment Media Preparation

Isotropic Sample

The first sample to be observed is an isotropic sample. You may want to dilute the isotropic sample by one third (to 75% of its original concentration) to match the concentration of most aligned samples. In the case of a weak dimer, this may be important.

PEG Bicelle

Alignment of the protein sample in PEG(C12E5/hexanol) is used as a first alignment media because it produces primarily steric alignment (useful in dimer geometry predictions), the success rate is high, and it can be doped with other charged detergents to give a second alignment media .

Chemicals used for this preparation:

Sigma Aldrich 76437, Pentaethylene glycol monododecyl ether (C12E5 PEG)
Sigma Aldrich H13303, Hexanol
Sigma Aldrich 855820, Cetyltrimethylammonium bromide (CTAB)
Sigma Aldrich O4003, Sodium octyl sulfate (SOS)

The preparation procedure is as follows:

  • Prepare the 16% PEG stock solution by first mixing 50µl of C12E5 (pentaethylene glycol monododecyl ether) with 200µl of buffer and 50µl of D2O by vortexing.[1]
  • Add approximately 16µl of hexanol to the stock solution, in aliquots of 2µl with vortexing after each addition. The solution will go from clear to milky, then to translucent and viscous with lots of bubbles. Continue to add hexanol until the solution goes clear again. If it becomes milky/turbid again, you have gone past the nematic phase.
  • Sample Content (for 220 µL sample):
145 µL of Protein stock solution
55 µL of 16% PEG stock solution
20 µL of D2O
Final PEG concentration is 4.2%.
  • Record the 2H splitting by running the s2pul expt with tn='lk' (for Varian instruments). The range of the splitting should be around +/-20Hz.
  • PEG can be doped with either cetyltrimethyl ammonium bromide (CTAB) for positively charged proteins or sodium octyl sulphate (SOS) for negatively charged proteins. Charging the medium to be like the protein prevents association and gives higher resolution spectra. A suitable ratio of PEG:CTAB/SOS is ~30:1.

Pf1 Phage

Preparation of a Pf1 phage alignment sample is fairly straightforward.[2] The protein sample is diluted by the alignment medium.

Chemicals used for this preparation:

ASLA Biotech P-50-P, Pf1 phage 50 mg/mL

The preparation procedure is as follows:

  • Start with a protein stock 0.5-1mM and a pf1 phage stock of 50 mg/mL. Prepare a sample of 12.5 mg/mL of phage.
  • Sample Content (for 220 µL sample):
145 µL of Protein stock solution
55 µL of Pf1 phage 50 mg/mL stock solution
20 µL of D2O
Final phage concentration is 12.5 mg/mL
  • Record the 2H splitting by running the s2pul expt with tn='lk' (for Varian instruments). The range of the splitting should be around +/-8-10 Hz.

Polyacrylamide Gel (Compressed and Stretched)

The preparation of polyacrylamide gel samples is a two step process. First the gels must be polymerized, equilibrated to the correct pH and cut to the appropriate size before being dried. Second the gels are re-hydrated using the protein stock in the appropriate NMR tube.

Chemicals used for this preparation:

Bio-Rad 161-0144, 40% Acrylamide/Bis solution 19:1
Bio-Rad 161-0733, 10X TBE
Bio-Rad 161-0700, APS
Bio-Rad 161-0800, TEMED
Sigma Aldrich M7279, N,N'-methylenebisacrylamide (BIS)
Sigma Aldrich 448281, (3-Acrylamidopropyl)trimethylammonium chloride solution
Sigma Aldrich 282731, 2-Acrylamido-2-methyl-1-propanesulfonic acid

Other materials used for this preparation:

Wilmad P-4.4965M-6.5135-0-0, 4.4965mm +/-0.0065mm ID x 6.5135mm +/-0.0065mm. Ground polished and buffed OD. 40mm +/- 0.5mm long. Both ends wet saw cut only.
Preparation of Dried Acrylamide Gels

The preparation procedure is as follows:

  • Prepare the positively and negatively charged 40% 19:1 bis:acrylamide solutions.
  • Positively charged stock solution (2mL):
31 mg of N,N'-methylenebisacrylamide (BIS)
961 µL of (3-acrylamidopropyl)trimethylammonium chloride solution
1039 µL of H2O
  • Negatively charged stock solution (2mL):
31 mg of N,N'-methylenebisacrylamide (BIS)
802 mg of 2-acrylamido-2-methyl-1-propanesulfonic acid
2000 µL of H2O
Standard formulas for preparing compressed and stretched polyacrylamide gels
Gel type  % acrylamide  % charged Vol. 40% charged stock solution (µL) Vol. 40% neutral stock solution (µL) Vol. 10x TBE (µL) Vol. 10% APS (µL) Vol. TEMED (µL) Vol. per casting tube (µL) Type of casting tube
charged compressed 7 50 43.75 43.75 400 7.5 5 140 2.8 mm ID  plastic
charged stretched 5 50 62.5 62.5 860 10 5 300 3.2 mm ID  glass
neutral stretched 5 0 0 125 860 10 5 490 4.5 mm ID  glass

Note: The APS solution should be prepared fresh and polymerization will begin as soon as TEMED is added.


  • Mix stock solutions of neutral and charged 40% acrylamide/bis 19:1 to achieve the desired overall charge ratio.
  • Dilute the mixtures 10x with TBE buffer (0.9 M TRIS, 0.9 M borate, 0.02 M EDTA, pH 8.2) to a final 7% or 5% concentration for compressed or stretched gels, respectively.
  • Polymerization is initiated by the addition of ammoniumperoxide sulfate (APS) (0.15% or 0.1% for compressed or stretched, respectively) and tetramethylethylenediamine (TEMED) (0.1% or 0.05% for compressed or stretched, respectively).
  • Pipet the mixture into the casting tubes carefully, to avoid bubbles, and keep them 1-2 hrs, allowing polymerization to occur.
  • Use a 200 µL pipet with a trimmed pipet tip (to avoid hitting the gel) and water to carefully push the compressed gels out of the casting tubes into a 1L Erlenmeyer flask filled with deionized water. For the stretched gels, use a 1000 µL pipet to carefully push the stretched gels out of the casting tubes into prepared racks (no more than 4-5 gels per rack) braced in 2L nalgene beakers filled with deionized water.
  • Wash the polymerized gels extensively in deionized water (two cycles over a period of 1 day). The gels will increase in size due to electro-osmotic swelling. Use cheesecloth to drain the water from the flask for the compressed gels. Be careful when draining and adding new deionized water not to damage the gels. The racks holding the stretched gels may be moved to a new 2L nalgene beaker with fresh deionized water.
  • Equilibrate the polymerized gels to the desired pH (to match the pH of the protein stock) by washing extensively in buffered solution (two cycles over a period of 1 day). The buffer should not contain only the major buffering species and no salts.
  • Wash the polymerized gels in deionized water overnight to allow them to swell to full size.
  • Select the gels which have no cracks or imperfections and measure the diameter of the fully swollen gels and trim each gel to a length 5.7 times its diameter.
  • Dry the gels over a 2 day period at room temperature on a teflon pan. If the gels do not dry well (straight, uniform width), but do not break, you can add a few drops of deionized water to slightly rehydrate them and allow them to dry again.
Preparation of Aligned Compressed Gel Samples
  • Sample content (compressed gel):
    1 dried compressed gel equilibrated to the same pH as the protein stock
    200 µL of Protein stock
    20 µL of D2O
  • Measure a height of 12-13 mm for the sample volume in a 5 mm shigemi tube and mark with a sharpie.
  • Add one dried compressed gel to the tube, followed by the protein stock and D2O.
  • Insert the plunger to the marked height and hold in place with parafilm.
  • Allow the gel to swell in the fridge for 1 day. Inspect the final sample for cracks before collecting data.
Preparation of Aligned Stretched Gel Samples

Chemicals used for this preparation:

Sigma Aldrich 440272, Dichlorodimethylsilane

Other materials required for this preparation:

Wilmad 528-PP-2.8mm/Stem, 528-PP NMR tube sealed to a 50mm long stem section (stem dimensions 2.8mm +/-0.025mm ID x wall 0.38mm +/-0.015mm). Overall length, 8 inches. Both ends open.
Wilmad 528-PP-3.6mm/Stem, 528-PP NMR tube sealed to a 50mm long stem section (stem dimensions 3.6mm +/-0.025mm ID x wall 0.38mm +/-0.015mm). Overall length, 8 inches. Both ends open.
Wilmad 528-PP-3.9mm/Stem, 528-PP NMR tube sealed to a 50mm long stem section (stem dimensions 3.9mm +/-0.025mm ID x wall 0.38mm +/-0.015mm). Overall length, 8 inches. Both ends open.
Wilmad 5mm microprobe NMR tube style, Upper tube 528-PP section 7 inches long sealed to a 50mm long stem section (427-PP). Both ends open.
  • Sample content (stretched gel):
    1 dried stretched gel equilibrated to the same pH as the protein stock
    300 µL of Protein stock
    20 µL of D2O
  • Prepare an NMR tube by washing the inside 3 times with dichlorodimethylsilane, then rinse with deionized water and dry.
  • Place a dried stretched gel near the top of the 5mm end of the NMR tube and attach a syringe with tubing to the bottom of the tube.
  • Carefully pipet in the protein stock and D2O allowing the solution's surface tension to hold it in place in the tube.
  • Use the syringe to adjust the position of the solution, such that the gel is centered in the column of solution. Cap the NMR tube, and let swell at room temperature 1-2 days. Capping the tube may cause the solution to shift, it's position should be readjusted with the syringe, to keep the gel centered.
  • Once the gel is swollen, use the syringe to gently pull the gel down to the lower stem of the tube. Insert a small rubber stopper in the bottom of the tube to prevent the gel from drying. Carefully insert a shigemi plunger in the top of the tube, to the top of the gel or the bottom of the upper stem, whichever is higher.


References

  1. Ruckert M and Otting G (2000), JACS, 122, 7793-7797
  2. Hansen MR, Mueller L, Pardi A (1998), Nat Struct Biol, 5, 1065-1074



Updated by Hsiau-Wei Lee, 2011

Updated by Kari Pederson, 2013