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Transcript of REALLY DIFFICULT PROTEIN MIXTURES: Prions to Proteomics · 7/8/2003 · REALLY DIFFICULT PROTEIN...
![Page 1: REALLY DIFFICULT PROTEIN MIXTURES: Prions to Proteomics · 7/8/2003 · REALLY DIFFICULT PROTEIN MIXTURES: Prions to Proteomics Andrew J. Alpert, Ph.D. PolyLC Inc. Columbia, MD U.S.A.](https://reader030.fdocuments.net/reader030/viewer/2022041200/5d30fa1788c9937b5d8d67df/html5/thumbnails/1.jpg)
HPLC OFREALLY DIFFICULT
PROTEIN MIXTURES:Prions to Proteomics
Andrew J. Alpert, Ph.D.PolyLC Inc.Columbia, MD U.S.A.
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TRADITIONAL BIOCHEMISTRY METHODS:Isolation: Keep enzymes active; resolve proteins.
Detergents; nonvolatile salts; urea or Gd.HCl (for solubility)Analysis: Gel electrophoresis (1- or 2-D); enzyme assays.
CURRENT REQUIREMENTS:
Isolation: Not necessary in many cases; MS can handle mixtures. Objective: Reduce large mixture to small mixtures. Identification not dependent on enzymes being active.
Analysis: MS: Volatile solvents required.Chromatography: Organic solvents, yes; detergents, no.
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ALTERNATIVES TO REVERSED-PHASE
1) Separation by chargea. Anion-exchange (WAX; SAX)b. Cation-exchange (WCX; SCX)
2) Separation by polaritya. Hydrophobic Interaction (HIC)b. Hydrophilic Interaction (HILIC)
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Polysuccinimide
Aminopropyl-silica___
Poly(succinimide)-silica_____
Poly(asparticacid)- silica _
(PolyCAT A)
Preparation ofa Weak
Cation-Exchange(WCX) material
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NEUROTROPHIC FACTOR:Polyethylene Glycol (PEG) Attached
0
0.008
0.016
0.024
0.032
0 .04
0.048
0 5 10 15 20 25 30 35
Abs
orba
nce
T im e (m in utes)
N -term in al PE G
PE G ylation varian ts
M u lti P EG ylated m o no m e r
COLUMN: PolyCAT A
-sensitive to both number of ligands and position of attachment -
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ION-EXCHANGE OF PROTEINS WITH ORGANIC SOLVENTS
Sample: recα-Bungarotoxinfrom P. Pastoris
- SelectivityIncreasesdramatically –
- data courtesy of Robert Rogowski and Edward Hawrot (Brown Univ.) -
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ION-EXCHANGE WITH ORGANIC SOLVENTS- rec Human Growth Hormone -
40% ACN
0% ACN
COLUMN:PolyCAT A
MOBILE PHASE:Salt gradient,pH 4.0
- data courtesy of Benny Welinder, Novo Nordisk -
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Hydrophilic Interaction Chromatography (HILIC) of Amino AcidsCOLUMN: PolySULFOETHYLAspartamide, 200x4.6-mm
Mobile Phase: 5 mM TEAP,pH 2.8, in 80% ACN
Order of elution:Least to most polar
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HYDROPHILIC INTERACTION CHROMATOGRAPHYOF AMINO ACIDS
(scx) (Neutral)
COLUMNS:200 x 4.6 mm;5-µm, 300-Å
MOBILE PHASE: 25 mM TEAP, pH 5.0, with ACN as noted
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15 20 25
A 210
A 210
A 210
0% ACN
40% ACN
70% ACN
p2
p1 + p0p2
p3
p0p1
p3
CEX-HILIC OF HISTONE H1.1COLUMN:PolyCAT A
SAMPLE:PhosphorylationVariants
TIME (min)
Protaminesulfate
0 5 10 30 35 40
COURTESY OF HERBERT LINDNER, UNIV. INNSBRUCK
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min0 10 20 30 40 50 60 70
mAU
-20
0
20
40
60
80
100
120
140
DAD1 B, Sig=215,4 Ref=off (K:\HPCHEM\4\DATA\20516A5\003-0401.D)
Surfactant Protein Variants
Lecithins, steroids, & other lipids
SCX-HILIC of LungSurfactant Protein(lipid:protein = 500:1)
COLUMN: PolySULFOETHYL A,200x4.6-mm; 5-µm; 1000-Å
MOBILE PHASE (1 ml/min):5’ hold, then 0-100% B in 60’
A) 0.1% methylphosphonic acid + 5 mM NaClO4, pH 3, with 70% ACN
B) Same but 100 mM NaClO4DETECTION: A215
SAMPLE: 24 µg protein/80 µl
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Hydrophilic Interaction Chromatography (HILIC)- works well for membrane proteins -
Removal of SDS, Coomassie Blue, and Salts from an ElectroelutedMembrane Protein
- data courtesy of Paul Jenö, Univ. of Basel -
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RPC-HILIC Purification of Variant Glycopeptidesfrom a Tryptic Digest of γ-Interferon
HILIC of Glycopeptide Asn-97 HILIC of Glycopeptide Asn-25
PolyHYDROXYETHYL A (150x1.0-mm)
RPC (Vydac C-18) of total digest from CHO batch culture
ADJACENT PEAKSDIFFER BY ONE
CARBOHYDRATERESIDUE OR
POSITION
Data courtesy of J. Zhang and D. Wang (MIT)
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HPLC of β-Amyloid Peptide (1-43)
HILICREVERSED-PHASE
AGGREGATES
AMYLOIDPEPTIDE
TRUNCATEDSEQUENCE
p-CRESOL
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PREPARATION OF SCRAPIE PRION PROTEIN
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HILIC of Scrapie Prion Protein1.0
0.8
Abs
orba
nce
280n
m 0.6
PrPSC
0.4
0.2
0.0
0 5 10 15 20 25 30
Time (minutes)
Column: PolyHYDROXYETHYL AGradient: Decreasing [ACN]
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EXTRACTION OF PRION PROTEIN BY HILIC
Blood Buffy coatcells
DNase Proteinase K
Na2SO4
H2O
Di- & tripeptidesPrion protein(PrPSC)
HFIP
HILIC Mobile FormicPhase A
Prion protein (PrPSC) inHILIC Mobile Phase B;
Dry and store orimmunoassay
Dryacid
SPE cartridge ofPolyHYDROXYETHYL A™
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+ + +
Antibody+ Peptide
Free Peptide
AggregatedPeptide
PeptideNonprion
Protein
PrionProtein
Antibody
Peptide only Antibody + peptide Negative sample Positive sample(control) (peak heights differ > 30%)
COMPETITIVE IMMUNOASSAY OF SCRAPIE PRION BY CE.Elapsed time of each electropherogram: 4’.
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y = 0.6635 - 0.0118 xR = - 0.955
0 10 20 30 400.0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8Sa
mpl
e ra
tio /
cont
rol r
atio
pg of recombinant bovine PrP
Cutoff point of positivetests, at ~ 2 pg rec PrP
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RFU
SEC OF FLUORESCENT PRION PEPTIDE + ANTIBODY
COLUMN: 104HY0505 (PolyHYDROXYETHYL A™; 500-Å)
FLOW: 0.25 ml/min0.130
0.135
FREEPEPTIDE
IMMUNOCOMPLEX
PEPTIDEONLY
0.125
0.120
0.115
0.110
0.105
1 20.100
3 4 5 6
time in minutes
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PROTEOMICS ANALYSES“A butterfly and a caterpillar have the same genome but different proteomes.” - Ron OrlandoTechniques for resolving complex protein mixtures:1) (TRADITIONAL) 2-Dimensional gel electrophoresis.2) (NEW) Digest the proteins with trypsin, identify the peptides via tandem
mass spectroscopy (MS/MS), and search a genome database to identifythe original proteins.
a) Need >15 fmol of each peptide, and < 15 peptides per scan window(~ 10”) or they’ll suppress each other’s ionization.
b) 16-300 Peptides: Use an RPC capillary to break up the peptides intosets of < 15 peptides per scan window.
c) 300-12,000 Peptides: 2-D LC: Use SCX to break up the peptides intosets [same charge-different polarity] small enough for RPC to handle.
d) >12,000 Peptides : 3-D LC needed.3) OBJECTIVE: Elution of components uniformly throughout the run, not to
get individual sharp peaks. Ugly chromatograms may actually containthousands of sharp peaks.
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CATION-EXCHANGE OF PEPTIDES (SCX)
PolySULFOETHYLAspartamide
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PEPTIDE PURIFICATION BY A CHARGE-POLARITY SEQUENCE
ADVANTAGES OF A SCX-RPC SEQUENCE:1) Capacity of SCX is 4x higher than RPC; better for first step2) RPC step desalts the SCX fractions
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Always be alert Always be alert and then wait. and then wait. Perhaps what Perhaps what you're looking you're looking for, will find for, will find you...you...
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PROTEOMICS BY 2-DIMENSIONAL LC/ MS/MSMudPIT: Multidimensional Protein Identification Technology
Typically identifies 2.5-3 peptides per protein; rugged method.Good where sample size is limited
ADVANTAGES OVER 2-DELECTROPHOPHORESIS
1) Greater dynamic range:Most abundant protein detectedLeast abundant protein detected
2) Works better for hydrophobic andvery basic proteins
3) Handling and automation easier
- from Link et al., Nat. Biotechnol. 17 (1999) 676-682 -
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WHY USE TRYPTIC PEPTIDES FOR PROTEOMICS ANALYSES?At pH 3, Asp- and Glu- are uncharged and all peptides have thesame charge: +2 (Exceptions: Peptides with His-, -S-S- bridges, theC-terminal peptide, etc.); should elute within a narrow window inSCX. Also, good size for MS/MS (< 20 residues, typically).
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SCX of Tryptic Digest of HeLa Cells:Retention Time vs. Charge
0
100
200
300
400
500
600
700
0 10 20 30 40 50 60 70 80
1+2+3+4+
NOTE: Y-Axis = number of peptides identified in each fraction, not the total number in the fraction. There are many more peptides in the +2 group than in the others.
- Data courtesy of Steven Gygi (Harvard Medical School) -
COLUMN: PolySULFOETHYL A (item# 202SE0502)
C-Term.,NAc-Term.,
Phospho-peptides,
etc. Peptides with His-, Lys-Lys, Lys-Pro, etc.
“Regular” Trypticpeptides
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Analysis of Yeast Proteome by SCX-RPC-MS/MS
Stro
ng C
ation
Exc
hang
e (SC
X)
(Poly
SULF
OETHYL
ATM
)
Tryptic TotalYeast Extract
IDENTIFIED:12,000 peptides1,600 proteins
Reversed phase chromatography - MS/MS of collected SCX fractions(COURTESY OF STEVEN GYGI & JUNMIN PENG, HARVARD MEDICAL SCHOOL)
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STRATEGY FOR PROTEOMICS ANALYSES
1) KEEP FRACTIONS SMALL
a) Peptides suppress each others’ ionization ∴ Better MS spectra obtained with less peptides.
b) Decreases chances of a high-abundance peptide sharing a fraction - and MS scan window - with a low-abundance peptide.
2) OFFLINE FRACTION COLLECTION SUPERIOR TO ONLINE
a) Permits larger SCX columns ( ↑ loading) and faster flow rates; facilitates collection of smaller, more numerous fractions.
b) Permits inclusion of 25% ACN in SCX buffers sharper peptide peaks ↑% peptides eluting in a single collected fraction ↑sensitivity to low-abundance peptides (NOTE: Not compatible with C-18 trap cartridges)
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Comparison of On-Line vs. Off-LineSCX of Peptides in 2-D LC/ MS/MSSample: LysC/Trypsin digest of rat liver microsomes
250 µg digested protein loaded
∴ 2x more peptides identified with off-line SCX!
Off-line SCX 513 Peptides
01020304050607080
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
Fraction
Num
ber o
f Pep
tides
SCX Buffers: Buffer A - 5mM KH2PO4, 5% MeCN, pH 3Buffer B - 5mM KH2PO4, 5% MeCN, pH 3, 500mM KCl
Gradient : 1-25% B in 25 minutes, 25-50% B in 10 minutes
COLUMN: PolySULFOETHYL A, 50x1.0-mm
SCX Buffer: 5mM KH2PO4, pH 3, 5% MeCN, X mM KCl
On-Line SCX 298 Peptides
01020304050607080
FT10
mM
25mM
35mM
50mM
60mM
75mM
100m
M20
0mM
1000
mM
Salt Steps
Num
ber o
f Pep
tides
- data courtesy Kevin Blackburn, Glaxo SmithKline -
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PROTEOMICS OF REALLY COMPLEX MIXTURESASSUMPTIONS:
1) 5000 PROTEINS IN THE MIXTURE (YIELDING 40,000 TRYPTIC FRAGMENTS)
2) AVERAGE MOL. WT. OF PROTEINS = 30 KDa
3) YOU NEED AT LEAST 15 FMOL TO GET A PEPTIDE SEQUENCE VIA MS/MS
∴YOU NEED (450 pg OF EACH PROTEIN) x (5000 PROTEINS) = 2.25 µg TOTAL PROTEIN
HOWEVER, PROTEINS DIFFER BY 106 IN REL. ABUNDANCE. NOW ASSUME RELATIVELY FEW PROTEINS MAKE UP MOST OF THE SAMPLE. TO GET 15 FMOL OF THE LEAST ABUNDANT PROTEIN, YOU WILL NEED AT LEAST 105 MORE SAMPLE:
2.25 µg x 105 = 225 mg TOTAL PROTEIN NEEDED
THIS REQUIRES A LARGE SCX COLUMN TO PROCESS. EVEN IF YOU DECREASE #PEPTIDES 90% VIA ICAT® [usually done after SCX], THAT STILL LEAVES 22.5 mg TO PROCESS
∴ 1) BIG MISMATCH BETWEEN SIZE OF SCX AND RPC COLUMNS
2) NEED TO COLLECT AND PROCESS 500+ FRACTIONS AT SCX STEP?
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Be determined in achieving your Be determined in achieving your goals...goals...
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Cell surface antigens, receptorsand membrane proteins (11.2%)
Channel proteins (4.9%)
Kinases and phosphatases (5%)
GTPases and GTP binding proteins (4.7%)
Ribosomal proteins (8.8%)
Mitochondrial proteins (5.1%)
Golgi /ER proteins (4.7%) Hypothetical proteins (14.1%)
Cytoskeletal proteins (4.5%)
Metabolic enzymes (15%)
Functionally uncharacterized proteins (22%)
Possibletransmembrane
Possible
transmembrane
Distribution of Proteins in Microsomal Extract,Identified via SCX-RPC-MS/MS- from Han et al., Nat. Biotechnol. 19 (2001) 946-951
Proteomics of Really Complex Mixtures:Simplification Through Organelle Isolation
PROBLEMS: 1) Contamination by other organelles2) Membrane proteins underrepresented (15-30% of total)
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Alternative strategies to 2DE are MS-based and involve multiple separation steps
1st dimension 2nd dimension 3rd dimension Acronym
Chait and colleagues
Gygi, Lee, Mann, etc.
Yates and colleagues
Isobe and colleagues
2DGESDS-PAGEIEF
RP- µLC
RP- µLCSAX-LC
MuDPIT
geLC-MS
RP- µLCSCX-LC
RP-µLCSDS-PAGE
SDS-PAGERP-LC
Proteins trypsinized to peptides
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Peak 2
Orlando Model: 3-D LC-MS/MSRPC (steep gradient; 10 fractions)
SCX of Peak 2 (10 fractions)
RPC (shallow gradient) of SCX fraction# 1;5 peptides identified
Fraction #1
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PROTEOMICS OF REALLY COMPLEX MIXTURESAlternative to organelle fractionation or n-D LC of peptides:
Predigest fractionation of proteins by HPLC
TISSUE OR CELL EXTRACT
HIC or anion/cation exchange
HILIC
Membrane-bound proteins;durable proteins (histones;growth factors; etc.)[several fractions]
Hydrophilic or delicateproteins (enzymes, etc.)[several fractions]
tryptic digestion tryptic digestion
SCX-RPCsequence
SCX-RPC orSCX-HILICsequence
Identification ofpeptides by MS/MS
Identification ofpeptides by MS/MS
HILIC or IEX-
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Mixed-Bed IEX of Cell Extract ProteinsCOLUMN (WCX): PolyCAT A, 200x4.6-mm; 5-µm, 1000-Å
GUARD CARTRIDGE (WAX): PolyWAX LP, 10x4-mm; 5-µm, 1000-Å
GRADIENT (40’ linear): 0-0.6 M NaCl in 10 mM KH2PO4, pH 6.2,with 5% ACN
DETECTION: Fluorescence (λex = 280 nm; λem = 350 nm)
WCX Column only (big void vol. peak)
WCX Column + WAX Cartridge (* = acidic proteins?)
* ** * *
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Mixed-Bed IEC of Intact Proteins fromTHP-1 Monocyte Cell Lysate
(~ 6x106 cells; water-soluble fraction)Columns: PolyCAT A/ PolyWAX LP Gradient: NaClO4 A280
- Data courtesy of Leticia Cano (City of Hope) -
THESE HIGH-ABUNDANCE PROTEINS SHOULD BE COLLECTED & LOCKED UP IN THEIR OWN FRACTIONS SO THEIR PEPTIDES WON’T MASK OTHERS.
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-25
0
25
50
75
Milli
volts
0.0 5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0MinutesColumn: PolyHYDROXYETHYL A (item# 204HY0503), HILIC mode. Detection: A220
Gradient: 40’ linear, 0-70% B. A) 15 mM TEAP, pH 2.7, with 85% ACNB) " " 10 "
SPE OF PEPTIDES:Selective Extraction by Carbon and C18 NuTips
= Transferrin tryptic digest (30 µg)= Peptides extracted/released by NT200C18 from 500 µg digest= " " NT200CAR " "= " "
(second set of releasing washes)
Urea(1 M)
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-50
-25
0
25
Milli
volts
0.0 5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0Minutes
SPE EXTRACTION OF PEPTIDES:Retention of specific peptides selectively depletes them from the mixture
Column: PolyHYDROXYETHYL A (item# 204HY0503), HILIC mode. Detection: A220Gradient: 40’ linear, 0-70% B. A) 15 mM TEAP, pH 2.7, with 85% ACN
B) " " 10 "
= Transferrin tryptic digest (30 µg)
= Transferrin tryptic digest; ~ 5 µg of remainder afterextraction of 50 µg digest with NT200C18
= Peptides extracted/released by NT200C18 from the 50 µg
Urea (1 M)
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0.7 - 1.8950,000IgM
0.8 - 2.9180,000 -500,000
IgA2 - 452,000α1-Antitrypsin3 - 780,000Transferrin
13.5 - 23150,000IgG52 - 6866,000Albumin
G. per 100 g. serum proteins
Mol. Wt.(Da)
Protein
SELECTIVE PRECIPITATION TO REMOVEPROTEINS OF HIGH ABUNDANCE
PROTEIN CONTENT OF SERUM
These six proteins represent ~ 90% of the total protein in serum(disregarding lipoproteins). All have mol. wt. > 50,000 Da.
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SEC of Crude Serum
0 10 20 30 40TIME (Min.)
COLUMN: PolyHYDROXYETHYL A (item# 209HY0503, two in series)
MOBILE PHASE: 100 mM KH2PO4, pH 6.6
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Serum + Acetonitrile- SEC of Supernatants Post-Centrifugation -
Crude Serum
Serum:ACN = 1:1
Serum:ACN = 1:2
Serum:ACN = 1:3
HSA
IgG?
IgM?
0 10 20 30 40 50TIME (Min.)
With 1 vol. ACN, ~ 97% of proteins > 40 KDa are removed. HSA is still the most abundant protein, though.
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Serum + Acetonitrile- SEC of TopTip™ Filtrates -
Serum:ACN = 1:1
Serum:ACN = 1:2
Serum:ACN = 1:3
SEC Standards
IgM(900 KDa)
IgG(150 KDa)
α-MelanocyteStimulatingHormone(1665 Da)
Leu-Enkeph-alinamide(555 Da)
Ovalbumin(46 KDa) α-Lactalbumin
(14.2 KDa)
Ubiquitin(8.5 KDa) Prion protein peptide [res.
218-232], FITC-labelled(2214 Da)RNase
A (13.7KDa)
HSA
IgG?IgM?
0 10 20 30 40 50TIME (Min.)
Filtration is 10x more effective than centrifugation. The 1:1 supernatant is rich in proteins < 30 KDa.
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Suggestions for Analysis of Whole Cellsand Membrane Proteins
1) DISSOLVE PELLET IN HFIP:FORMIC ACID = 60:40.
2) FRACTIONATE/DELIPIDATE VIA HILIC OR MIXED-BED IEX-HILIC.
3) LYOPHILIZE FRACTIONS; REDISSOLVE PROTEINS IN (MINIMAL) HFIP AND SLOWLY ADD WATER/PrOH. 4) DIGEST FRACTIONS WITH TRYPSIN USING 30% PrOH/NH4HCO3
a) Digestion more thorough than with urea, esp. for membrane proteins. Ref.: Russell et al., Anal. Chem. 73 (2001) 2682-2685, and ASMS 2002 poster# T005 [limit digests obtained in 6’].
b) Effect of ~ 5% HFIP: Slows trypsin’s action; ~ 16-20 hr required to get a limit digest, not 6-60’.
4) REALLY HYDROPHOBIC TRANSMEMBRANE PEPTIDES:Try SCX-HILIC instead of SCX-RPC.
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Delipidation of Whole CellLysates via HILIC1
NEEDED: PolyHYDROXYETHYL A™ SPE cartridge [PolyLC item# SPEHY1203]. Lysates (approx. 2 x 107
cells) or CNBr-digested lysates (approx. 4 x 107 cells) were loaded in 90% organic and eluted in steps of 70%, 40%, 20%, 0% and again 0% organic solvent.Loading/flushing solution: 20mM ammonium formate, 90% ACN, 0.1% HFIPEluting solution: 0.2% formic acid, 0.1% HFIP.
1 A.J. Alpert, J. Chromatogr. 499 (1990) 177-196
THIS METHOD ALSO ELIMINATES DETERGENTS, SALTS, AND VARIOUS REAGENTS. GOOD CLEANUP STEP.
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Removal of 8.6% SDS from Peptide by SPE-HILICSample: Penetratin [RQIKIWFQNRRMKWKK]
SPE Cartridge: TopTip, item# TT200HEA (HILIC mode)
HPLC Column: Vydac 218TP104 (C-18); ACN gradient in 0.1% TFA
- Data courtesy of Britt-Marie Olsson (Stockholm Univ.) -
PENETRATIN PEAK
after SPE before SPE
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