Phosphorylation and SDS PAGE question

Jim Woodgett jwoodget at oci.utoronto.ca
Tue Nov 7 09:55:52 EST 1995


In article <Pine.SOL.3.91.951107143359.6565A-100000 at sun1.oulu.fi>, Petri 
Kursula <pkursula at cc.oulu.fi> writes:
  
> A question to somebody with experience: How much does the 
> phosphorylation of a protein affect its movement on SDS PAGE? Is 
> the difference significant, say could it be that the protein seems 
> about 2000 da larger than it is supposed to because it has 
> been phosphorylated? 

Yes and no.  It all depends on the particular protein and the gel system you 
use.  The mobility shift is an artefact caused by a reduction in SDS-binding 
to the protein (presumably close to the phosphorylation sites). However, in 
some cases a single phosphorylation site can cause a 10 kDa shift, in others 
multiple sites have no effect.  SOme gel systems allow high resolution, others 
lose the differences.

You can't rely on a shift being due to phosphorylation (other 
posttranslational modifications can shift mobilities) and you can't rule out 
phosphorylation if a shift doesn't occur.  If you suspect phosphorylation try 
the following experiments:

1. Treat your protein sample with purified phosphatase (alkaline or acid or 
PP-1 or 2A) +/- pyrophosphate to inhibit the p'tase.  If the band shifts to a 
faster mobility you're likely dealing with phosphorylation.

2.  32P Phosphate label your cells and immunopurify the protein.

3.  If its cloned, express the protein in bacteria.  Often proteins aren't 
modified in bugs which thus provides a source of "apo-protein".

4.  If you have it clean enough and its not too big try FAB-MS as this 
generates a more reliable mass.

5.  If you suspect the protein is phosphorylated on tyrosine immunoblot it 
with anti-pTyr antibodies (commercially available).

Examples of shifting proteins:

c-Jun phosphorylated at serine 63/73 -> 39 kDa to 43 kDa
Erk-2 phosphorylated at tyrosine and threonine -> 42 kDa -> 44kDa

Examples of non-shifting proteins:

c-Jun phosphorylated at three C-terminal sites
c-Myc phosphorylated at numerous sites (very small change)

Check out Methods in enzymology vols 200 and 201 for techniques in protein 
phosphorylation.  There's also a new Practical Approach book on the same 
topic.

Jim Woodgett



-> ->   !!!!!!!!!New Address!!!!!!!!!!  <- <-
Ontario Cancer Institute, 610 University Avenue, Toronto, Ontario M5G 2M9, Canada
Fax: (416) 946-2963  or (416) 946-6529  Tel: (416) 946-2962
mailto:jwoodget at oci.utoronto.ca
Kinases R Us




More information about the Methods mailing list