Protein blot (Western)

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[[Image: ECL detection WB.jpg|thumb|Traditional ECL image utilizing a chemiluminescent substrate to react with HRP, producing light that exposes the film in a band pattern]]
[[Image: ECL detection WB.jpg|thumb|Traditional ECL image utilizing a chemiluminescent substrate to react with HRP, producing light that exposes the film in a band pattern]]
-
[[Image: Time Course1.jpg|right|A classic time course study; harvest cells at sequential time points to measure changes in protein expression]]
+
[[Image: Time Course1.jpg|thumb|A classic time course study; harvest cells at sequential time points to measure changes in protein expression]]
A '''protein blot''', also known as the '''immunoblot''' or '''Western blot''', is a method of semiquantitative determination of protein expression. Crude cell lysates are loaded into a polyacrylamide gel containing a denaturing agent which give all the proteins a net negative charge. A current passing through the gel will then propel the proteins through the gel, with the largest proteins travelling the slowest. This results in the proteins being roughly separated by their mass. The proteins are then transferred from the gel onto a membrane (often nitrocellulose or PVDF), which is then incubated with an antibody directed against the protein of interest. By using a detector conjugated to an antibody one can then specifically detect the protein of interest.
A '''protein blot''', also known as the '''immunoblot''' or '''Western blot''', is a method of semiquantitative determination of protein expression. Crude cell lysates are loaded into a polyacrylamide gel containing a denaturing agent which give all the proteins a net negative charge. A current passing through the gel will then propel the proteins through the gel, with the largest proteins travelling the slowest. This results in the proteins being roughly separated by their mass. The proteins are then transferred from the gel onto a membrane (often nitrocellulose or PVDF), which is then incubated with an antibody directed against the protein of interest. By using a detector conjugated to an antibody one can then specifically detect the protein of interest.
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*Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
*Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
-
*Transfer proteins to a nitrocellulose or PVDF membrane and block in fresh 5% milk TTBS 2 hr room temperature, or overnight at 4C.
+
*Transfer proteins to a nitrocellulose or PVDF membrane and block the membrane in 10 cm square dish with fresh 5% milk TTBS 2 hr room temperature, or overnight at 4C.
*Perform 3-5 shake rinses with cold TTBS (until no residual milk is observed).
*Perform 3-5 shake rinses with cold TTBS (until no residual milk is observed).
-
*Incubate the primary antibody 1:200 in fresh 1% milk/1% BSA TTBS for 90 minutes room temperature.
+
*Incubate the primary antibody 1:200 in fresh 3% milk TTBS for 90 minutes room temperature.
*Perform 3 shake rinses, followed by 4X for 5 minutes washes with ambient or cold TTBS.
*Perform 3 shake rinses, followed by 4X for 5 minutes washes with ambient or cold TTBS.
*Incubate the the secondary antibody 1:1000 anti-mouse in fresh 1% milk TTBS for 60 minutes at room temperature.
*Incubate the the secondary antibody 1:1000 anti-mouse in fresh 1% milk TTBS for 60 minutes at room temperature.
*Perform 3 shake rinses, followed by 4X for 5 minutes washes with ambient or cold TTBS.
*Perform 3 shake rinses, followed by 4X for 5 minutes washes with ambient or cold TTBS.
*Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.  
*Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.  
 +
*Prepare the membranes for ECL by covering with either saran wrap, or a transparency page. There should be no running of ECL liquid.
*Optimize protein signal with multiple exposure times.
*Optimize protein signal with multiple exposure times.
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* Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
* Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
-
* Transfer proteins to a nitrocellulose or PVDF membrane and block the membrane in fresh 5% milk TTBS 2 hr room temperature, or overnight at 4C.
+
* Transfer proteins to a nitrocellulose or PVDF membrane and block the membrane in 10 cm square dish with fresh 5% milk TTBS 2 hr room temperature, or overnight at 4C.
* Perform 3-5 shake rinses (until very little residual milk washes off the membrane).
* Perform 3-5 shake rinses (until very little residual milk washes off the membrane).
* Incubate membrane with the primary antibody 1:200 in fresh 5% Milk TTBS for 90 minutes room temperature.
* Incubate membrane with the primary antibody 1:200 in fresh 5% Milk TTBS for 90 minutes room temperature.
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* Perform shake rinses, until no residual milk is observed, followed by 4X 5 minute wash with ambient or cold TTBS.
* Perform shake rinses, until no residual milk is observed, followed by 4X 5 minute wash with ambient or cold TTBS.
* Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.
* Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.
 +
* Prepare the membranes for ECL by covering with either saran wrap, or a transparency page. There should be no running of ECL liquid.
* Optimize protein signal with multiple exposure times.
* Optimize protein signal with multiple exposure times.
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*Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
*Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
-
*Transfer proteins to a nitrocellulose or PVDF membrane and block in fresh 5% milk TTBS 2 hr, r.t. or overnight at 4C.
+
*Transfer proteins to a nitrocellulose or PVDF membrane and block in 10 cm square dish with fresh 5% milk TTBS 2 hr, r.t. or overnight at 4C.
*Perform 3 shake rinses (until very little residual milk washes off the membrane).
*Perform 3 shake rinses (until very little residual milk washes off the membrane).
*Incubate the primary antibody 1:200 in fresh 3% milk TTBS for 90 minutes room temperature.
*Incubate the primary antibody 1:200 in fresh 3% milk TTBS for 90 minutes room temperature.
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*Perform 3 shake rinses, followed by 4X 5 minute wash with ambient or cold TTBS.
*Perform 3 shake rinses, followed by 4X 5 minute wash with ambient or cold TTBS.
*Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.
*Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.
 +
*Prepare the membranes for ECL by covering with either saran wrap, or a transparency page. There should be no running of liquid.
*Optimize protein signal with multiple exposure times.
*Optimize protein signal with multiple exposure times.
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====Dephosphorylation of Lysate with Lambda Phosphatase====
====Dephosphorylation of Lysate with Lambda Phosphatase====
-
1. To a micro-centrifuge tube add 80 µg of lysate. Amount maybe scaled up or down as needed.
+
=====Lysate Treatment=====
-
2. Add 6 microliters of l- PPase Buffer. Final concentration: 50 mM Tris, pH 7.5, 0.1 mM Na2EDTA, 5 mM dithiothreitol, 2 mM MnCl2.  
+
*To a micro-centrifuge tube add 80 µg of lysate. Amount maybe scaled up or down as needed.  
 +
*Add 6 microliters of lambda-PPase Buffer. Final concentration: 50 mM Tris, pH 7.5, 0.1 mM Na2EDTA, 5 mM dithiothreitol, 2 mM MnCl2.
 +
*Add 400 units of l-Phosphatase
 +
[http://www.scbt.com/datasheet-200312.html Santa Cruz Biotechnology Inc.] sc-200312
-
3. Add 400 units of l-Phosphatase ([http://www.millipore.com/ Millipore] Cat. #14-405)
+
[http://www.millipore.com/ Millipore] Cat. #14-405  
-
4. Incubate at 30˚C for 20 minutes.  
+
*Incubate at 30˚C for 20 minutes.  
-
 
+
*The protein sample/lysate is now ready for analysis or further preparation depending on application  
-
5. The protein sample/lysate is now ready for analysis or further preparation depending on application  
+
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#Paper1 pmid=12137799
#Paper1 pmid=12137799
</biblio>
</biblio>
 +
 +
=====Membrane Treatment=====
 +
 +
Treats ~30 lanes or 2-3 (6x12 cm) membranes. Mark treated and untreated membranes.
 +
 +
* Block membranes in 3%BSA, 1X TBS, 0.1% Triton X-100.
 +
* Add 15 ul of Lambda-PPase (Santa Cruz Biotechnology Inc. sc-200312) in 15 ml of blocking buffer + 2mM DTT, 2mM MnCl2.
 +
* Incubate submerged membrane @ room temp 4hr, or 4C ON.
 +
* Wash 2x  1X PBST.
 +
* Wash 2x  dH2O.
 +
* 1ary incubation / 2ary incubation / wash / ECL.
 +
 +
==Heat dependent antigens==
 +
 +
Certain antigens (caveolin-1) have been reported to be heat sensitive in SDS-PAGE analysis. Antigen sensitivity may be improved by adjusting lysis heating parameters from
 +
 +
95C for 3-5 minutes
 +
 +
TO
 +
 +
70C for 10 minutes
==Transfer tips for high molecular weight proteins==
==Transfer tips for high molecular weight proteins==
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*Do not let the gel sit in transfer buffer for prolonged periods prior to transfer.  
*Do not let the gel sit in transfer buffer for prolonged periods prior to transfer.  
*Transfer for 16 hours at 30 Volts, then 1 hour at 100 Volts.  Do not exceed 220  mAmps.  
*Transfer for 16 hours at 30 Volts, then 1 hour at 100 Volts.  Do not exceed 220  mAmps.  
-
*PVDF may be used instead of nitrocellulose.
+
*O.45 um PVDF or nitrocellulose may be effective.
 +
 
 +
==Transfer tips for low molecular weight proteins==
 +
 
 +
Tricine Gels are ideal for protein separation from 2.5-50 kDa.
 +
 
 +
*Tricine Gel
 +
*Gradient 10-20%
 +
*0.1 or 0.05um PVDF or 2 pieces of 0.2 micron PVDF
 +
*lower transfer time relative to standard transfer time
 +
 
 +
===Tricine Gel===
 +
 
 +
Tricine ions migrate ahead of the smallest proteins. This improves the resolution of low molecular weight proteins. Tricine gels display good transfer efficiency, in a lower pH. 
 +
 
 +
[http://depts.washington.edu/taneli/procedure/tris_tricinel.PDF Tricine Gel Recipe]
==Protein Deglcyosylation==
==Protein Deglcyosylation==
 +
 +
[[Image: Protein Glycosylation.jpg|thumb|N-link carbohydrate chains (light blue) influence the actual surface contour of membrane bound proteins (green/red) that harbor them]]
 +
 +
Glycosylation of proteins and lipids is a post-translational modification important for numerous physiological processes; protein folding, ligand binding, cell surface contour, and influencing cell–cell and cell–matrix interactions. 
In order to determine the presence and/or significance of protein glycosylation, the carbohydrate chains may be removed by catalysis.  
In order to determine the presence and/or significance of protein glycosylation, the carbohydrate chains may be removed by catalysis.  
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N-Glycosidase F (PNGase F) is a ~36 kDa amidase that cleaves at the innermost N-acetylglucosamine (GlcNAc) and asparagine residues of high mannose, hybrid, and complex oligosaccharides from N-linked glycoproteins.
N-Glycosidase F (PNGase F) is a ~36 kDa amidase that cleaves at the innermost N-acetylglucosamine (GlcNAc) and asparagine residues of high mannose, hybrid, and complex oligosaccharides from N-linked glycoproteins.
-
===PNGase F kits===
+
*PNGase F
 +
*Endo-O-Glycosidase
 +
*a-2(3,6,8,9)-Neuraminidase (Sialidase A)
 +
*ß(1,4)-Galactosidase
 +
*ß-N-Acetylglycosaminidase
 +
 
 +
 
 +
(1) Tarentino, A.L. and Plummer, T.H., Jr. (1994) Methods in Enzymology, 230: 44-47. PMID: 8139511
 +
 
 +
===Deglycosylation kits===
 +
 
 +
 
 +
Enzymes and reagents combined into convenient to use kits exist in order to remove N-linked and O-linked carbohydrates from glycoproteins, and cleave complex core O-linked carbohydrates (including polylactosamine). Deglycosylation can simplify SDS-PAGE by decreasing the potential broad size variation associated with glycoproteins.
 +
 
[http://www.neb.com/nebecomm/default.asp New England Biolabs] offers a convenient kit Cat#P0704S.
[http://www.neb.com/nebecomm/default.asp New England Biolabs] offers a convenient kit Cat#P0704S.
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==Troubleshooting==
==Troubleshooting==
-
[[Image: WB titration.jpg|thumb|Diluting the primary antibody further and including 5% milk TTBS would reduce the overall signal and improve the clarity of the major bands. Adjusting the exposure time may also improve this result.]]
+
[[Image: WB titration.jpg|thumb|Diluting the primary antibody further out in 5% milk TTBS would reduce the overall signal and improve the clarity of the major bands. Adjusting the exposure time & additional shake rinse after 2ary incubation will help]]
-
 
+
[http://openwetware.org/wiki/Griffin:Western_Blot_Optimization Western Blot Optimization]
[http://openwetware.org/wiki/Griffin:Western_Blot_Optimization Western Blot Optimization]
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The western blotting procedures are the same for PVDF or nitrocellulose, however the handling of these membranes are different prior to- and during- transfer of proteins from the SDS-PAGE gel to the membrane.  
The western blotting procedures are the same for PVDF or nitrocellulose, however the handling of these membranes are different prior to- and during- transfer of proteins from the SDS-PAGE gel to the membrane.  
 +
 +
===Nitrocellulose===
Nitrocellulose exhibits the highest sensitivity with very low backgrounds in all transfers, especially in protein blotting. Unlike PVDF, nitrocellulose wets out naturally, does not require methanol, and will not turn hydrophobic during the transfer process. Nitrocellulose is very easily blocked and does not need the many blocking steps required with PVDF. Protocols for Western Blotting with PVDF and Nitrocellulose are the same with a few exceptions.  
Nitrocellulose exhibits the highest sensitivity with very low backgrounds in all transfers, especially in protein blotting. Unlike PVDF, nitrocellulose wets out naturally, does not require methanol, and will not turn hydrophobic during the transfer process. Nitrocellulose is very easily blocked and does not need the many blocking steps required with PVDF. Protocols for Western Blotting with PVDF and Nitrocellulose are the same with a few exceptions.  
-
PVDF is hydrophobic and therefore should be prewet in methanol before it is used. Wet the membrane in methanol for 15 seconds. Membrane should uniformly change from opaque to semi-transparent. Carefully place the membrane in ultrapure water and soak for 2 minutes. Then carefully place the membrane in transfer buffer and let equilibrate for at least 5 minutes. Another change to note is that the SDS tolerances are not equivalent for PVDF and Nitrocellulose. The binding of protein to PVDF is much more sensitive to SDS levels. Too much SDS can inhibit the protein's ability to bind to the PVDF and can, in fact, help proteins already bound to the membrane to slip off. SDS levels should never exceed 0.05% for PVDF.
+
===PVDF===
 +
 
 +
[http://en.wikipedia.org/wiki/Polyvinylidene_fluoride Polyvinylidene Fluoride] is hydrophobic and should be prewet in methanol before it is used.  
 +
 
 +
*Wet the membrane in 100% methanol for 15 seconds. The membrane should uniformly change from opaque to semi-transparent.  
 +
*Place the semi-transparent membrane into ultrapure water and soak for 5 minutes.
 +
*Place the membrane into transfer buffer and soak for at least 5 minutes.  
 +
*Transfer proteins to the smooth/reflective side that has more shine
 +
 
 +
Another change to note is that the SDS tolerances are not equivalent for PVDF and Nitrocellulose. The binding of protein to PVDF is much more sensitive to SDS levels. Too much SDS can inhibit the protein's ability to bind to the PVDF and can, in fact, help proteins already bound to the membrane to slip off. SDS levels should never exceed 0.05% for PVDF.
==Membrane Stripping==
==Membrane Stripping==
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==Stability of reagents==
==Stability of reagents==
-
* Ammonium persulphate/persulfate (APS) is a very reactive compound (used for radical generation in the polymerisation process). It is prone to oxidation and loss of activity which will increase your polymerisation times. Make small aliquots, keep in the cold. [http://www.bio-medicine.org/biology-technology/Acrylamide-Polymerization--A-Practical-Approach-1090-4/]
+
* Ammonium persulphate/persulfate (APS) is a very reactive compound (used for radical generation in the polymerisation process). It is prone to degradation and loss of activity which will increase your polymerisation times. Make small aliquots, keep in the cold. [http://www.bio-medicine.org/biology-technology/Acrylamide-Polymerization--A-Practical-Approach-1090-4/]
* TEMED, the catalyst of polymerisation, is also prone to oxidation especially if mixed with water which it attracts if the container is left open. Seal quickly, keep in cold place. [http://www.bio-medicine.org/biology-technology/Acrylamide-Polymerization--A-Practical-Approach-1090-4/] [http://www.sigmaaldrich.com/catalog/search/SpecificationSheetPage/SIGMA/T9281]
* TEMED, the catalyst of polymerisation, is also prone to oxidation especially if mixed with water which it attracts if the container is left open. Seal quickly, keep in cold place. [http://www.bio-medicine.org/biology-technology/Acrylamide-Polymerization--A-Practical-Approach-1090-4/] [http://www.sigmaaldrich.com/catalog/search/SpecificationSheetPage/SIGMA/T9281]
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* acrylamide/bis-acrylmide is a neurotoxin. Handle with precaution. [http://www.jtbaker.com/msds/englishhtml/a1553.htm]
* acrylamide/bis-acrylmide is a neurotoxin. Handle with precaution. [http://www.jtbaker.com/msds/englishhtml/a1553.htm]
* TEMED is very corrosive. Most likely exposure in the lab due to inhalation. Reseal the container as quickly as possible. [http://www.jtbaker.com/msds/englishhtml/t2080.htm]
* TEMED is very corrosive. Most likely exposure in the lab due to inhalation. Reseal the container as quickly as possible. [http://www.jtbaker.com/msds/englishhtml/t2080.htm]
-
==See also==
 
-
* [[Protein blot (Western) hub]]
 
-
* [http://en.wikipedia.org/wiki/Western_blot Western blot on the Wikipedia]
 
==Curators==
==Curators==
[[User:Korey Griffin]]
[[User:Korey Griffin]]
-
 
-
[[Category:Protocol]] [[Category:In vitro]] [[Category:Protein]]
 

Revision as of 18:23, 18 November 2011

A visual representation of loading protein sample onto a polyacrylamide gel
A visual representation of loading protein sample onto a polyacrylamide gel
Coommassie stained protein gel showing a visual representation of protein separation by weight
Coommassie stained protein gel showing a visual representation of protein separation by weight
Traditional ECL image utilizing a chemiluminescent substrate to react with HRP, producing light that exposes the film in a band pattern
Traditional ECL image utilizing a chemiluminescent substrate to react with HRP, producing light that exposes the film in a band pattern
A classic time course study; harvest cells at sequential time points to measure changes in protein expression
A classic time course study; harvest cells at sequential time points to measure changes in protein expression

A protein blot, also known as the immunoblot or Western blot, is a method of semiquantitative determination of protein expression. Crude cell lysates are loaded into a polyacrylamide gel containing a denaturing agent which give all the proteins a net negative charge. A current passing through the gel will then propel the proteins through the gel, with the largest proteins travelling the slowest. This results in the proteins being roughly separated by their mass. The proteins are then transferred from the gel onto a membrane (often nitrocellulose or PVDF), which is then incubated with an antibody directed against the protein of interest. By using a detector conjugated to an antibody one can then specifically detect the protein of interest.

Contents

Standard western blot procedure

Transient SLUG gene expression in 293GP cells (last lane); titration of the primary and adjusting exposure time will improve the signal:noise
Transient SLUG gene expression in 293GP cells (last lane); titration of the primary and adjusting exposure time will improve the signal:noise

Prior to running the western blotting experiment, consult with the vendor in order to determine if they have optimized the titration for the antibody you just purchased. Most vendors should offer some guideline for how to use the antibody. Value your time and effort first and foremost. If the experiment comes out strange, make the call or email the vendor for assistance. Your time is the most valuable element to the procedure!

Mouse monoclonal western blot

  • Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
  • Transfer proteins to a nitrocellulose or PVDF membrane and block the membrane in 10 cm square dish with fresh 5% milk TTBS 2 hr room temperature, or overnight at 4C.
  • Perform 3-5 shake rinses with cold TTBS (until no residual milk is observed).
  • Incubate the primary antibody 1:200 in fresh 3% milk TTBS for 90 minutes room temperature.
  • Perform 3 shake rinses, followed by 4X for 5 minutes washes with ambient or cold TTBS.
  • Incubate the the secondary antibody 1:1000 anti-mouse in fresh 1% milk TTBS for 60 minutes at room temperature.
  • Perform 3 shake rinses, followed by 4X for 5 minutes washes with ambient or cold TTBS.
  • Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.
  • Prepare the membranes for ECL by covering with either saran wrap, or a transparency page. There should be no running of ECL liquid.
  • Optimize protein signal with multiple exposure times.

Goat polyclonal western blot

  • Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
  • Transfer proteins to a nitrocellulose or PVDF membrane and block the membrane in 10 cm square dish with fresh 5% milk TTBS 2 hr room temperature, or overnight at 4C.
  • Perform 3-5 shake rinses (until very little residual milk washes off the membrane).
  • Incubate membrane with the primary antibody 1:200 in fresh 5% Milk TTBS for 90 minutes room temperature.
  • Perform 3 shake rinses, followed by 4X 5 minute wash with ambient or cold TTBS.
  • Incubate the the secondary antibody 1:5000 anti-goat in fresh 5% Milk TTBS for 60 minutes at room temperature.
  • Perform shake rinses, until no residual milk is observed, followed by 4X 5 minute wash with ambient or cold TTBS.
  • Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.
  • Prepare the membranes for ECL by covering with either saran wrap, or a transparency page. There should be no running of ECL liquid.
  • Optimize protein signal with multiple exposure times.

Rabbit polyclonal western blot

  • Load at least 50 ug of whole cell lysate or 20 ug nuclear extract prepared from fresh buffers (30 µg of protein ~ 25,000 cells). Resolve proteins on the gel voltage gradient.
  • Transfer proteins to a nitrocellulose or PVDF membrane and block in 10 cm square dish with fresh 5% milk TTBS 2 hr, r.t. or overnight at 4C.
  • Perform 3 shake rinses (until very little residual milk washes off the membrane).
  • Incubate the primary antibody 1:200 in fresh 3% milk TTBS for 90 minutes room temperature.
  • Perform 3 shake rinses, followed by 4X 5 minute wash with ambient or cold TTBS.
  • Incubate the the secondary antibody 1:4000 anti-rabbit in fresh 1% Milk TTBS for 60 minutes at room temperature.
  • Perform 3 shake rinses, followed by 4X 5 minute wash with ambient or cold TTBS.
  • Perform ECL using a suitable detection reagent. Wick away all residual chemiluminescent liquid by dabbing membrane edges on paper towel.
  • Prepare the membranes for ECL by covering with either saran wrap, or a transparency page. There should be no running of liquid.
  • Optimize protein signal with multiple exposure times.

Phosphorylation state specific western blot

Adjusting certain incubation conditions can improve the detection signal for the phospho-specific antibody. When serine/threonine phosphatase inhibitor Sodium Fluoride (NaF), and tyrosine phosphatase inhibitor Sodium Orthovanadate (Na3VO4) are included in the blocking and incubation buffers, phospho-specific signals can noticeably improve. Including 50 mM NaF and 5 mM Na3VO4 in the blocking and incubation buffers can improve the signal. Using 5% milk diluent for primary and secondary incubations will reduce the nonspecific banding and background.

  • Load 50 ug of whole cell lysate/tissue extract OR 20 ug of nuclear extract prepared from fresh buffers. Resolve proteins on the gel voltage gradient.
  • Transfer proteins to a nitrocellulose or PVDF membrane and block in fresh 5% milk TTBS, 50 mM NaF/5 mM Na3VO4 for 2 hr, r.t. or overnight at 4C. Perform 3 shake rinses and drain until no residual milk appears to stream off the wash buffer.
  • Incubate the primary antibody 1:200-20000 in fresh 5% milk TTBS, 50 mM NaF/5 mM Na3VO4 for 120 minutes room temperature. Perform 3 shake rinses followed by wash with cold TTBS 4X for 5 minutes each wash.
  • Incubate the the secondary antibody 1:2000 anti-mouse, 1:5000 anti-rabbit, 1:5000 anti-goat in fresh 5% milk TTBS, 50 mM NaF/5 mM Na3VO4 for 60 minutes at room temperature. Perform 3 shake rinses followed by wash with cold TTBS 4X for 5 minutes each wash.
  • Perform ECL using a suitable chemiluminescent reagent
  • Optimize protein signal with multiple exposure times.

Dephosphorylation of Lysate with Lambda Phosphatase

Lysate Treatment
  • To a micro-centrifuge tube add 80 µg of lysate. Amount maybe scaled up or down as needed.
  • Add 6 microliters of lambda-PPase Buffer. Final concentration: 50 mM Tris, pH 7.5, 0.1 mM Na2EDTA, 5 mM dithiothreitol, 2 mM MnCl2.
  • Add 400 units of l-Phosphatase

Santa Cruz Biotechnology Inc. sc-200312

Millipore Cat. #14-405

  • Incubate at 30˚C for 20 minutes.
  • The protein sample/lysate is now ready for analysis or further preparation depending on application


  1. Sharma SK and Carew TJ. . pmid:12137799. PubMed HubMed [Paper1]
Membrane Treatment

Treats ~30 lanes or 2-3 (6x12 cm) membranes. Mark treated and untreated membranes.

  • Block membranes in 3%BSA, 1X TBS, 0.1% Triton X-100.
  • Add 15 ul of Lambda-PPase (Santa Cruz Biotechnology Inc. sc-200312) in 15 ml of blocking buffer + 2mM DTT, 2mM MnCl2.
  • Incubate submerged membrane @ room temp 4hr, or 4C ON.
  • Wash 2x 1X PBST.
  • Wash 2x dH2O.
  • 1ary incubation / 2ary incubation / wash / ECL.

Heat dependent antigens

Certain antigens (caveolin-1) have been reported to be heat sensitive in SDS-PAGE analysis. Antigen sensitivity may be improved by adjusting lysis heating parameters from

95C for 3-5 minutes

TO

70C for 10 minutes

Transfer tips for high molecular weight proteins

Standard protein transfer

1) Perform electrophoresis on 8-15% acrylamide SDS-PAGE gel, according to standard procedures.

2) Transfer proteins onto a nitrocellulose membrane, overnight (approximately 18 hours) at 0.1 Amp.

3) Running Buffer: 50 mM Tris: 6.06 g Tris Base, 380 mM Glycine: 28.5 g Glycine, 1.6 mM EDTA: 0.67 g EDTA (tetra Na is the most soluble), 0.1% SDS: 1.0 g SDS

4) Transfer buffer: 50 mM Tris, 380 mM glycine, 0.1% (w/v) SDS, 10% (v/v) methanol. Final pH: 8.3.

Adjustments to consider for high molecular weight proteins

  • 6% acrylamide gel is preferable with high molecular weight proteins.
  • Use 15-20% methanol in transfer buffer. Methanol strips the SDS off of the proteins, which changes the charge of the proteins. Methanol also causes the gel to shrink.
  • Do not let the gel sit in transfer buffer for prolonged periods prior to transfer.
  • Transfer for 16 hours at 30 Volts, then 1 hour at 100 Volts. Do not exceed 220 mAmps.
  • O.45 um PVDF or nitrocellulose may be effective.

Transfer tips for low molecular weight proteins

Tricine Gels are ideal for protein separation from 2.5-50 kDa.

  • Tricine Gel
  • Gradient 10-20%
  • 0.1 or 0.05um PVDF or 2 pieces of 0.2 micron PVDF
  • lower transfer time relative to standard transfer time

Tricine Gel

Tricine ions migrate ahead of the smallest proteins. This improves the resolution of low molecular weight proteins. Tricine gels display good transfer efficiency, in a lower pH.

Tricine Gel Recipe

Protein Deglcyosylation

N-link carbohydrate chains (light blue) influence the actual surface contour of membrane bound proteins (green/red) that harbor them
N-link carbohydrate chains (light blue) influence the actual surface contour of membrane bound proteins (green/red) that harbor them

Glycosylation of proteins and lipids is a post-translational modification important for numerous physiological processes; protein folding, ligand binding, cell surface contour, and influencing cell–cell and cell–matrix interactions.

In order to determine the presence and/or significance of protein glycosylation, the carbohydrate chains may be removed by catalysis.

N-Glycosidase F (PNGase F) is a ~36 kDa amidase that cleaves at the innermost N-acetylglucosamine (GlcNAc) and asparagine residues of high mannose, hybrid, and complex oligosaccharides from N-linked glycoproteins.

  • PNGase F
  • Endo-O-Glycosidase
  • a-2(3,6,8,9)-Neuraminidase (Sialidase A)
  • ß(1,4)-Galactosidase
  • ß-N-Acetylglycosaminidase


(1) Tarentino, A.L. and Plummer, T.H., Jr. (1994) Methods in Enzymology, 230: 44-47. PMID: 8139511

Deglycosylation kits

Enzymes and reagents combined into convenient to use kits exist in order to remove N-linked and O-linked carbohydrates from glycoproteins, and cleave complex core O-linked carbohydrates (including polylactosamine). Deglycosylation can simplify SDS-PAGE by decreasing the potential broad size variation associated with glycoproteins.


New England Biolabs offers a convenient kit Cat#P0704S.

Sigma Aldrich offers the PNGase F enzyme Cat#P7367.

Troubleshooting

Diluting the primary antibody further out in 5% milk TTBS would reduce the overall signal and improve the clarity of the major bands. Adjusting the exposure time & additional shake rinse after 2ary incubation will help
Diluting the primary antibody further out in 5% milk TTBS would reduce the overall signal and improve the clarity of the major bands. Adjusting the exposure time & additional shake rinse after 2ary incubation will help

Western Blot Optimization

Blocking: To block nonspecific sites on the membrane, incubate the membrane with blocking buffer (5% milk TTBS) prior to primary antibody incubation. 2 hour room temperature blocking is sufficient for the membrane to absorb proteins and minimize noise.

Primary antibody: Use a diluent containing a blocking protein (5% milk TTBS or 1%milk/1%BSA TTBS) to dilute the primary antibody.

Secondary antibody: Use a diluent containing a blocking protein (5% milk TTBS or 1%milk/1%BSA TTBS) to dilute the primary antibody. Performing a "Secondary control" control blot where the primary antibody is purposely omitted is useful for identifying whether nonspecific signals are due to the secondary antibody conjugate or the primary antibody.

Washes: All wash steps are critical for reducing general background signal and nonspecific binding to discrete bands. If high background is a problem, the number, length and composition of the washes can all be increased.

General: Handle membranes carefully with forceps to minimize problems with nonspecific signals. Wear gloves for all steps to prevent hand contact with film, membranes or detection reagents.

PVDF versus Nitrocellulose

The western blotting procedures are the same for PVDF or nitrocellulose, however the handling of these membranes are different prior to- and during- transfer of proteins from the SDS-PAGE gel to the membrane.

Nitrocellulose

Nitrocellulose exhibits the highest sensitivity with very low backgrounds in all transfers, especially in protein blotting. Unlike PVDF, nitrocellulose wets out naturally, does not require methanol, and will not turn hydrophobic during the transfer process. Nitrocellulose is very easily blocked and does not need the many blocking steps required with PVDF. Protocols for Western Blotting with PVDF and Nitrocellulose are the same with a few exceptions.

PVDF

Polyvinylidene Fluoride is hydrophobic and should be prewet in methanol before it is used.

  • Wet the membrane in 100% methanol for 15 seconds. The membrane should uniformly change from opaque to semi-transparent.
  • Place the semi-transparent membrane into ultrapure water and soak for 5 minutes.
  • Place the membrane into transfer buffer and soak for at least 5 minutes.
  • Transfer proteins to the smooth/reflective side that has more shine

Another change to note is that the SDS tolerances are not equivalent for PVDF and Nitrocellulose. The binding of protein to PVDF is much more sensitive to SDS levels. Too much SDS can inhibit the protein's ability to bind to the PVDF and can, in fact, help proteins already bound to the membrane to slip off. SDS levels should never exceed 0.05% for PVDF.

Membrane Stripping

Griffin:Membrane_Stripping_and_Reprobing

Stability of reagents

  • Ammonium persulphate/persulfate (APS) is a very reactive compound (used for radical generation in the polymerisation process). It is prone to degradation and loss of activity which will increase your polymerisation times. Make small aliquots, keep in the cold. [1]
  • TEMED, the catalyst of polymerisation, is also prone to oxidation especially if mixed with water which it attracts if the container is left open. Seal quickly, keep in cold place. [2] [3]

Toxicity of reagents

  • acrylamide/bis-acrylmide is a neurotoxin. Handle with precaution. [4]
  • TEMED is very corrosive. Most likely exposure in the lab due to inhalation. Reseal the container as quickly as possible. [5]

Curators

User:Korey Griffin

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