Workshop IIc Manual interpretation of MS/MS spectra Ebbing de Jong
Why MS/MS spectra? The information contained in an MS spectrum (m/z, isotope spacing and therefore z ) is not enough to tell us the amino acid sequence Luckily, peptides fragment in a predictable way and a spectrum of these fragments can help us figure out the sequence
OK how? 100,000 s of molecules of a particular peptide will be isolated and fragmented Each of these molecules will create a b / y ion pair in an MS/MS spectrum The spacing (mass difference) between peaks in an MS/MS spectrum is characteristic of the amino acid residue(s) differing between the two sequences
Residue masses
Relative intensity Relative intensity Easiest example Glycyl-glycine (GG) 100 90 80 70 60 50 40 30 20 10 0 minimal fragmentation [Gly + H] + 76.04 0 20 40 60 80 100 120 140 m/z [Gly-gly + H] + Δ m/z = 57.02 133.06 100 90 80 70 60 50 40 30 20 10 0 more fragmentation 76.04 [Gly + H] + [Gly-gly + H] + 133.06 0 20 40 60 80 100 120 140 m/z The spacing of these peaks (57.021 m/z) tells us that the heavier ion has an extra glycine residue compared to the lighter ion
b 2 ion is usually present Look for the b 2 /a 2 pair, Δ m/z = 28
Overlapping masses and neutral losses Neutral loss of H 2 O (-18) and NH 3 (-17) are relatively common
The Nine-Step Strategy for Interpretation (from Reference 1) 1. Inspect the low-mass region for immonium ions. The first step in the interpretation is to inspect the low-mass region of the spectrum, noting the presence of any immonium ions and the amino acid composition that they indicate. 2. Inspect the low-mass region for the b 2 -ion. In the second step of the interpretation, the low-mass region of the spectrum is inspected to identify the b 2 -ion, generally recognizable by the b 2 -ion / a 2 -ion pair separated by 28 Da. By using Table 4.2, the possible two-amino acid-combinations indicated by the b 2 -ion are noted. The m/z of the b 2 -ion is then used to calculate the m/z of the corresponding y n-2 -ion, and the high-mass region of the product ion spectrum is inspected to identify this ion. 3. Inspect the low-mass region for the y 1 -ion. The third step of the interpretation is to assign the C-terminal amino acid. The low-mass region of the spectrum is inspected to identify the y 1 -ion at either m/z 147, for C-terminal lysine peptides, or m/z 175, for C-terminal arginine peptides. The m/z of the y 1 -ion is then used to calculate the m/z of the b n-1 -ion, and the high-mass region of the product ion spectrum is inspected to identify that ion, if present. 4. Inspect the high-mass region to identify the y n-1 -ion. The fourth step of the interpretation is to attempt to assign the N- terminal amino acids from combinations indicated by the b 2 -ion. The high-mass region of the spectrum is scrutinized to identify the y n-1 -ion, if present. The list of possible amino acid combinations derived from the b 2 -ion limits the possible residue masses to consider. If an ion is identified the m/z of that ion is used to calculate the residue masses of the first two amino acids and to assign those peptides. 5. Extend the y-ion series toward lower m/z. Working with the residue masses listed in Table 4.1, begin to extend the y-ion series backwards (toward lower m/z) from the y n-2 -ion. As a y-ion is identified calculate the m/z of the corresponding b-ion and identify that ion in the spectrum. Work towards extending the y-ion series from the y n-2 ion to the y 1 -ion 6. Extend the b-ion series toward higher m/z. If progress extending the y-ion series falters, use the residue masses listed in Table 4.1 to extend the b-ion series from the last identified b-ion. As any b-ions are identified, use the m/z of that ion to calculate the m/z of the corresponding y-ion and identify that ion in the spectrum. 7. Calculate the mass of the peptide. When the interpretation of the spectrum is complete, calculate the mass of the proposed peptide sequence and check its agreement with the measured mass. 8. Reconcile the amino acid content with spectrum data. Check that the amino acid content agrees with the immonium ions observed. Also consider the charge state of the peptide in terms of the presence of histidine, and internal lysine or arginine residues. 9. Attempt to identify all ions in the spectrum. Work to identify the other ions in the spectrum based on the proposed peptide sequence and pay particular attention to the ions from the loss of H 2 O, NH 3, and HSOCH 3 ; any doubly charged ions; and any ions due to internal cleavages.
LeeAnn just showed you: Peptide MS/MS Spectrum Precursor [M + 2H] +2 698.86 m/z Charge state information is calculated from full scan hegem007_fanx0092_120812_12508_seed_soluble #3757 RT: 36.52 AV: 1 NL: 3.74E3 T: FTMS + c NSI d Full ms2 698.86@hcd40.00 [111.00-1410.00] 100 90 80 70 175.12 508.29 708.37 Relative Abundance 894.47 hegem007_fanx0092_120812_12508_seed_soluble #3755 RT: 36.50 AV: 1 NL: 1.11E5 T: FTMS + c NSI Full ms [360.00-1800.00] 698.86 z=2 100 90 80 70 60 50 40 30 20 10 0 Full scan 698.86 m/z precursor isotope series: z = 2 698.0 698.2 698.4 698.6 698.8 699.0 699.2 699.4 699.6 699.8 700.0 700.2 700.4 m/z 699.36 z=2 699.86 z=2 60 50 229.12 263.10 807.44 40 30 300.16 995.52 392.19 637.33 1082.55 20 10 337.11 463.16 951.49 550.16 1046.53 1196.59 1283.63 0 200 300 400 500 600 700 800 900 1000 1100 1200 1300 m/z
MS/MS Spectrum [M + 2H] +2 698.86 m/z 400 1400 m/z Calculate a Partial Amino Acid Sequence from the consecutive y-ion series hegem007_fanx0092_120812_12508_seed_soluble #3757 RT: 36.52 AV: 1 NL: 3.74E3 T: FTMS + c NSI d Full ms2 698.86@hcd40.00 [111.00-1410.00] 708.37 100 90 80 Start: [M + H] +1 1283.63 = (residue mass) 1283.63 1196.59 = (residue mass) 894.47 70 508.29 60 50 40 30 409.22 807.44 995.52 637.33 1082.55 20 10 1196.59 1283.63 0 400 500 600 700 800 900 1000 1100 1200 1300 m/z Further reference: http://www.ionsource.com/tutorial/denovo/b_and_y.htm
MS/MS Spectrum [M + 2H] +2 698.86 m/z Low m/z range hegem007_fanx0092_120812_12508_seed_s... 12/8/2012 11:43:13 PM hegem007_fanx0092_120812_12508_seed_soluble #3757 RT: 36.52 AV: 1 NL: 3.04E3 T: FTMS + c NSI d Full ms2 698.86@hcd40.00 [111.00-1410.00] 100 120.08 175.12 90 80 70 136.08 202.08 60 50 40 30 20 10 129.10 158.09 235.11 245.12 183.11 240.10 219.08 229.12 207.11 263.10 271.10 289.11 300.16 0 120 140 160 180 200 220 240 260 280 300 m/z
http://www.ionsource.com/card/immon/immon.htm
Diagnostic Low Mass Marker Ions in MS/MS Spectra Used for Peptide Sequence Interpretation Immonium Ion 2015 Regents Copied of the from University matrixscience.com of Minnesota. All rights reserved.
http://www.ionsource.com/card/aatable/aatable.htm
Example #2 bhering_dejon039_082912_12156_preitq_0989 #5252 RT: 38.96 AV: 1 NL: 9.80E4 T: FTMS + c NSI d Full ms2 821.89@hcd40.00 [111.00-1655.00] 288.20 100 95 90 85 80 75 70 258.11 175.12 169.13 159.09 65 60 55 50 45 40 35 30 25 20 15 10 5 0 185.09 213.09 1074.52 312.16 502.30 817.41 1003.48 440.22 1203.57 1314.60 444.27 617.33 1331.62 329.15 746.37 403.23 569.26 1185.56 640.29 1430.70 842.44 986.47 1296.58 1395.65 1527.78 200 300 400 500 600 700 800 900 1000 1100 1200 1300 1400 1500 1600 m/z
Example #3 tgriffin_dejon039_073013_13290_6c #4453 RT: 30.58 AV: 1 NL: 3.02E4 T: FTMS + c NSI d Full ms2 747.34@hcd40.00 [111.00-1505.00] 245.08 100 217.08 95 90 85 80 75 70 65 60 175.12 55 50 45 40 35 30 25 20 15 10 5 0 635.28 506.24 377.20 763.38 894.42 518.23 1008.46 1119.49 991.43 259.09 1136.52 389.18 360.17 617.27 468.19 746.35 773.36 312.16 596.25 1102.47 877.39 645.27 974.41 835.32 1069.74 1249.60 200 300 400 500 600 700 800 900 1000 1100 1200 1300 1400 1500 m/z
References 1. Protein Sequencing and Identification Using Tandem Mass Spectrometry: http://onlinelibrary.wiley.com/book/10.1002/0471721980 and especially chapter 4, Collisionally induced dissociation of protonated peptide ions and the interpretation of product ion spectra: http://onlinelibrary.wiley.com/doi/10.1002/0471721980.ch4/pdf 2. http://www.ionsource.com/tutorial/denovo/b_and_y.htm