Introduction of SILAC and its applications Stable Isotope Labeling of Amino acids in Culture Develop...
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Transcript of Introduction of SILAC and its applications Stable Isotope Labeling of Amino acids in Culture Develop...
Introduction of SILAC and its applications
• Stable Isotope Labeling of Amino acids in Culture
• Develop and promoted by Matthias Mann
• Two papers: – Lipid Rafts (PNAS)– Focal Adhesion precursors (Cell under review)
What does a mass spectrometer do?
Precise identification of massCan trap a single ion species and fragment to get subfragments (sequence)
Theoretically (database), know what the fragments should be (Trypsin digest)
Purify over monomeric avidin column(This is a selection/simplification scheme)
Ideally, should see ratios between state1 and state2 (they will have the same retention time).
Check to see if the mass is correct.
Reminder of ICAT technology
Expect to see a ratio between the peak sizes.
SCX profile
LC profile of a single fraction
Composite of SCX separation.
Overview of Biological and Chemical Isotope Labeling Strategis
Two complementary samples
Labeling
Analysis
Example:
Have large analysis space
SILAC vs. ICAT
• Culture system only• De Novo Proteins (no
serum contamination)• No optimization
• Simplifies MS/MS• More complete
peptide coverage
• ALL protein samples• Labels selected
moieties• Need to optimize
labeling• Large linker group.• Reduces complexity
“Light”
“Heavy”
“Light/heavy” mix
How can you distinguish between isotoped species?
Time-course of deuterated isoleucine incorporation.
Also gives you an indication of the robustness of the assay.Can compare the peak strength.
How do you actually get quantitation?
1) Once you’ve identified the complementary peptides, 2) Backtrack and integrate the Xtracted Ion Chromatogram
Two papers1) Unbiased Quantitative Proteomics of Lipid Rafts Reveals High Specificity for Signaling Factors
Foster LJ, de Hoog CL, Mann MPNAS, 2003
2) RNA and RNA-binding proteins participate in early stages of cell spreading through Spreading Initiation Centers, sites of nascent focal adhesion formation.
De Hoog CL, Foster LJ, Nielsen, MM, Mann M(Cell), pending
Experimental Strategy:
1) Grow cells with “heavy” or “light” until saturation (5 divisions)2) Add cholesterol depleting drugs (3 conditions)
1) Methyl-beta cyclodextrin2) Filipin3) nystatin
Biochemistry outline
1) Lyse cells by either TX-100 or pH11 buffer.2) Determine protein concentration and mix samples.3) Purify lipid rafts.4) Trypsinize5) MS/MS analysis
Example of 2 proteins:
Doublet recognition
Identity
Abundance ratios
Enriched Non-enriched
Global analysis of raft protein data:
MCD is most efficient at extractingcholesterol
Ratio between experimental/control population
Detergeant extractions:
1) MCD 2) Filipin3) Nystatin
4) Average pH extration
See sharp Cutoffs
This is the AMAZING table:Clear demarcation of
Raft proteinsAssociated ProteinsNon-specific proteins
ratios close to 1 (mostlyhigh abundance cellular proteins (biochemical background))
Serum proteins (not shown)
Raft proteins (1TM or fatty acid mod)Associated proteins (no TM, but associate)Positives and Negatives all make sense!!
Conclusions (from this paper and others):
Rafts enrich >10-fold for signalling proteins.Rafts bind not just tyrosine kinases but also serine/threonine
kinases and G proteins (more ubiquitous than thought)
Focal adhesion protocol overview.
Sample difference is attachmentThen IP with talin, vinculin, paxillin.
Isotoped peptide identification
Isotoped peptide characterization (talin)
Peptide quantification (.83)
Protein results summary:
304 proteins identified:Only a small number of proteins were attachment dependent.
(from SILAC quantitation data).
There are many problems holes in their quantitation data.I’m not up to giving them a hard time today.
Cell biology….Studied RACK1
Come back to what I think SILAC/ICAT criteria is…
-RACK1/vinculin interaction is greater in adherent cells (2.06).-In spread cells, they don’t colocalize.
However, when cells are DETACHED (1hr), then allowed to SPREAD, they begin to colocalize(2µm). (stage 1)Focal adhesion begin to appear under the colocalized spots (stage2)The cell spreads and colocalization disappears (stage3)
Similar results for paxillin, talin, and FAK
Actin forms a ring around this initial complex (SIC or spreading initiation complex).
This ringstructure is transient and gone by stage 3.
RNA binding proteins were found reproducibly in all 3 Ips.
The RNA-binding proteins hnRNP K, FUS/TLS, hnRNP E1, SmB, SmD, but NOT snRNP U1 were found in SICs.
SICs stain for nucleic acids. This is Rnase I sensitive.
In fully spread cells, don’t see splicesome components (part C).
SILAC vs. ICAT
• Culture system only• De Novo Proteins (no
serum contamination)• No optimization
• Simplifies MS/MS• More complete
peptide coverage
• ALL protein samples• Labels selected
moieties• Need to optimize
labeling• Large linker group.• Reduces complexity
Which method would you use? -SILAC can only be used in tissue culture. If you are doing this, it simplifies the question (vs. ICAT) GREATLY.
-Cell lines vs. tumors. Are the phenotypes and profiles from a tumor reflected on a dish?Can solve lack of antibody problem temporarily…
-3-dimensional growth. SILAC can eliminate background completely!-I believe this is the major advantage of SILAC (even without quantitation)
-Criteria before proteomics Proteomics is trivial/non-trivial!!! Just a glorified Western.Information overload.QUICK, CLEAN secondary screen.
Otherwise, proteomics is useless.Just come up with interesting, unverifiable data!!!
Matrigel is useful and simple/complex(~10mg/ml protein)