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Electron capture dissociation (ECD) studies of two modified Amyloid βpeptides (20–29 and 25–35) were performed to investigate the role of H• radicals in the ECD of peptide ions and the free radical cascade (FRC) mechanism. 2,4,6-trimethylpyridinium (TMP) was used as the fixed charge tag, which is postulated to both trap the originally formed radical upon electron capture and inhibit the H• generation. It was found that both the number and locations of the fixed charge groups influenced the backbone and side-chain cleavages of these peptides in ECD. In general, the frequency and extent of backbone cleavages decreased and those of side-chain cleavages increased with the addition of fixed charge tags. A singly labeled peptide with the tag group farther away from the protonated site experienced a smaller decrease in backbone cleavage fragments than the one with the tag group closer to the protonated site. Despite the non-protonated nature of all charge carriers in doubly labeled peptide ions, several c and z• ions were still observed in their ECD spectra. Thus, while H• transfer may be important for the N-Cα bond cleavage, there also exist other pathways, which would require a radical migration via H• abstraction through space, or via an amide superbase mechanism. Finally, internal fragment ions were observed in the ECD of these linear peptides, indicating that the important role of the FRC in backbone cleavages is not limited to the ECD of cyclic peptides.
In contrast with slow heating fragmentation methods such as infrared multiphoton dissociation (IRMPD)  and collisionally activated dissociation (CAD) , Electron capture dissociation (ECD)  of multiply charged peptide/protein ions is often considered as a “directed” tandem mass spectrometric (MS/MS) method since it non-specifically cleaves many backbone bonds while frequently leaving the more labile groups [4–8] and non-covalent interactions [9–13] intact. Because of these unique properties, it has significant applications in both top-down and bottom-up sequencings for protein identification [3, 7, 14–16], as well as in post-translational modification (PTM) characterization [4, 17, 18]. The ECD process is the dissociative recombination of multiply charged peptide/protein ions with low energy electrons [3, 17, 19]. The major products of the electron capture are often the charge reduced species, [M+nH](n−1)+ •, and the H• loss product, [M+(n−1)H](n−1)+ . There are two backbone fragmentation pathways: the major one produces c and z• (or c• and z) ions via N-Cα bond cleavage and the minor pathway generates a• and y ions [3, 17, 19]. In addition, ECD may also produce some amino acid side-chain cleavages [21–23] and secondary fragment ions [24–26].
Currently, two primary mechanisms have been proposed to explain the abundant c and z• type ions observed in the ECD spectra of peptides. In the dissociation-recapture mechanism, the initially captured electron in a high-lying Rydberg state may land in one of the protonated sites and the resultant H• from the dissociation of the neutralized ammonium group (or other charged groups) can be recaptured by a nearby carbonyl oxygen atom, yielding an aminoketyl intermediate that dissociates via the N-Cα bond cleavage . Since the cross section for gas phase peptide ions to capture a free hydrogen atom is low [19, 27], it was argued to be unlikely that the abundant backbone cleavages were induced by the mobile hot hydrogen from the neutralization of a charged amino or guanidine group. Such cleavages were probably initiated by a concerted dissociation-recapture process upon electron capture due to the extensive solvations of the charged sites by multiple backbone carbonyls, which may also be followed by secondary fragmentations . The low selectivity in backbone cleavages and preservation of labile groups during ECD were attributed to the non-ergodic nature of this process, i.e. the N-Cα bond cleavage occurs before the ~6 eV recombination energy was randomized among the 3N-6 normal vibrational modes in the peptide molecule via intramolecular vibrational energy redistribution (IVR), which would result in milli-eV’s of energy per mode, clearly far below the normal adiabatic bond dissociation energies [3, 17]. The non-ergodic premise has been scrutinized heavily as of late [19, 28], and the necessity of the presence of a hydrogen atom to initiate N-Cα bond cleavages was also under debate [8, 29]. In the recently proposed amide-superbase mechanism, it was argued that the electron is first captured in the remote-charge (Coulomb) stabilized π* orbital of a backbone carbonyl, generating an aminoketyl anion (a super base) which abstracts a nearby proton, and the resultant aminoketyl radical undergoes facile cleavage of the adjacent N-Cα bond with a very low (or nonexistent) energy barrier, thus eliminating the need to evoke non-ergodic hypothesis, as well as the necessity of the presence of a hydrogen atom [19, 30]. Furthermore, many H• abstraction reactions in peptides, in addition to having low activation barriers, also are net exothermic reaction, as the radical moves to a more stable site. It was further suggested that both mechanisms might be at work depending on the electronic states of the peptide ions [19, 31].
Either of these two mechanisms addresses only the formation of the c and z• type ions, but does not explain the many other types of fragment ions also present in the ECD spectra. In particular, in the ECD spectra of doubly charged cyclic peptide ions, many backbone fragment ions were observed, which requires multiple backbone cleavages by a single electron capture. It was proposed that these ions resulted from the free radical cascade (FRC), i.e., the radical site on the initially produced z• ion could initiate secondary fragmentations via hydrogen abstraction and/or loss of neutrals such as diketopiperazines . For linear peptides, hydrogen atom migrations within the post-ECD complex are also frequently observed. In an ECD study of peptides with all glycine alpha hydrogens replaced by deuterons, many fragment ions showed extensive H/D scramblings . Moreover, c• and z ion formations are common in peptide ion ECD spectra , which has been demonstrated to be the result of the intra-complex hydrogen transfer between the originally formed c/z• ion pair [13, 33, 34]. A double resonance (DR)-ECD experiment showed that a long-lived free radical intermediate existed in the ECD process , and that its lifetime was often much longer than the time it took for the intra-complex hydrogen transfer . However, evidence for multiple backbone cleavages resulting in the formation of internal ions in the ECD of linear peptide ions was lacking to date, most likely due to the location of charges near the termini for the tryptic peptides studied. Experimental evidence linking the formation of smaller z• ions to the FRC of larger ones was also lacking, as the resonant ejection of the latter during ECD did not lead to appreciable decrease in smaller z• ion abundances ; thus, if the FRC is to account for some of the smaller z• ion formation, it must have taken place on a timescale shorter than the ejection time (typically milliseconds). Nevertheless, the FRC may still play an important role in the ECD of linear peptides, as evidenced by the abundant secondary side-chain cleavages and radical rearrangement, particularly when there is extra energy deposited in the precursor ions [13, 24, 25, 35, 36].
The importance of the radical in ECD was investigated further by several research groups with added radical trap moieties in the peptide [37, 38]. In one study, coumarin labels were attached to the N-terminal and/or lysine side-chain amine groups to serve as radical traps, which appeared to inhibit the c/z ion formation while enhancing the side-chain cleavages in ECD . In another study, a 2-(4′-carboxypyrid-2′-yl)-4-carboxamide group (pepy) moiety was used as the stable trap for both the electron and the hydrogen, which resulted in abundant electron capture without backbone dissociation. When the precursor ions were preheated by an IR laser near the dissociation threshold, subsequent electron capture did trigger backbone dissociation, but only produced b type ions . These studies demonstrated the instrumental role of the mobility of the radical in peptide ion ECD.
In this study, a different radical trap, 2,4,6-trimethylpyridinium (TMP), was used. In addition to its potential of being a stable radical trap, TMP also functions as a fixed charge that inhibits the H atom formation upon electron capture and does not form hydrogen bonds with backbone carbonyls in the precursor ions. This may shed light on our understanding of both the primary and secondary ECD mechanisms. Charge derivatization methods using both positively and negatively charged derivatives have been used in mass spectrometry research to control the type of fragment ions generated from peptides and to facilitate the interpretation of the mass spectral data [39-44]. In several recent ECD and the related electron transfer dissociation (ETD)  studies, fixed charge derivatization was used to increase the sequence coverage, investigate the role of excited electronic states, study the effects of cation charge-site identity, and examine the mechanism of disulfide bond cleavages [31, 46-48].
Amyloid β peptides (20-29, FAEDVGSNKG, hereafter abbreviated as Aβ 20) and (25-35, GSNKGAIIGLM, hereafter abbreviated as Aβ 25) were purchased from Bachem AG (Philadelphia, PA) and used without further purification. 2,4,6-trimethylpyrylium tetrafluoroborate was purchased from Alfa Aesar (Ward Hill, MA). Poros 50 R1 material was purchased from Applied Biosystems (Foster City, CA). All other chemicals were purchased from Sigma (St. Louis, MO).
Potassium carbonate buffer solution (0.1 M K2CO3 and 0.1 M NaHCO3) containing ~0.05 M 2,4,6-trimethylpyrylium tetrafluoroborate was prepared, whose pH was adjusted to ~9 using ~10 μl of HCl. 20 nmol of each peptide was dissolved in 50 μl of this buffer solution respectively, vortexed, and purged with nitrogen gas. The reaction was allowed to proceed for 18–24 hrs at room temperature. The final reaction solutions were dried and the peptide derivatives were purified by Poros 50 R1 material in custom solid phase microextraction (SPME) tips. Each fraction of the eluate was analyzed, and unlabeled, singly-labeled, and doubly-labeled fractions were identified by electrospray ionization (ESI) Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR-MS, or FTMS).
Unlabeled, singly-labeled, and doubly-labeled model peptides were analyzed by ECD at ~10-5 M concentration in 49.5:49.5:1 methanol:water:formic acid spray solution. The ECD analysis was performed in a custom qQq-FT-ICR-MS equipped with an external nano-spray source and a 7 Telsa actively shielded superconducting magnet as described previously [49, 50]. Multiply charged precursor ions were isolated by the front-end quadrupole (Q1) followed by external accumulation in the collision cell (Q2) for about 100-600 ms, before they were transferred via two rf-only hexapoles and trapped in the ICR cell using the gated trapping. These trapped ions were then irradiated with low-energy electrons (~0.2 eV) for 50–120 ms, generated by the indirectly heated dispenser cathode (Heatwave, Watsonville, CA). A chirp excitation/detection sequence was used and the signal was averaged for 20 scans. All spectra were zero filled once without apodization and Fourier transformed to give the magnitude mode spectra. Internal calibration using the molecular ion and the charge reduced species gave a typical mass accuracy of less than 2 ppm for most of the peaks identified.
The derivatization reaction of peptides with 2,4,6-trimethylpyrylium was previously used to convert the β-amino group of the lysine side chain to the charged TMP group (Scheme 1) [51–53]. Even though each of the Amyloid β peptides studied here only has one lysine residue, some doubly tagged peptides were also produced, where the second tag must have gone to the N-terminal amino group. The singly tagged peptides may exist in one of the two forms, with either the lysine side-chain or the N-terminal amino group modified. Since the TMP tagging causes a mass shift of ~104 Da (from the charged amino group as it introduces a fixed charge) per modification, it was possible to localize the TMP group in the lysine residue rather than at the N-terminus (vide infra). The TMP group also fixed the charge at the nitrogen atom on the pyridinium ring, eliminating the existence of (relatively) free protons in the doubly tagged peptides, which allows the study of the role of hydrogen atom in the ECD process. Furthermore, the aromatic structure of the pyridinium ring could trap the radical generated near the TMP group, making it unlikely to propagate and induce further reactions.
Before analyzing the results obtained in the ECD studies of these modified peptides and attempting to draw conclusions on the ECD mechanism, it is important to point out that the modification also significantly changes the peptide conformational and electronic structures, which may influence the outcome of the electron capture, such as the preferential neutralization site and the ECD product branching ratios for different fragmentation channels.
The ECD spectra of the unlabeled, singly- and doubly-labeled Amyloid β peptides are shown in Figure 1 (Aβ 20) and Figure 2 (Aβ 25), with the insets showing the cleavage patterns for the corresponding peptides. ECD of the unmodified Aβ 20 gave rise to many c and z type ions (Figure 1a), reflecting the charge locations near both the N- and C-termini, as well as the similar recombination energy of the charged N-terminal amino group and the lysine side-chain. On the other hand, ECD of the unmodified Aβ 25, with both charges located near the N-terminus, produced mostly N-terminal (b- and c-type) ions, with the only z ion (z8) being the one that contains the lysine residue (Figure 2a). Some a and y ions were also present, likely the products of the minor channel in ECD that produces a- and y-type ions . In addition, abundant b ions were observed in both spectra, a phenomenon that was previously investigated by Copper et al., who found that the b ion formations were common in ECD of peptides, particularly those containing lysines but not arginines [25, 55]. Such would be the case if the electron capture deposited sufficient energy into the precursor ion that resulted in the formation of the excited [M+(n−1)H](n−1)+ ion (the hydrogen atom loss product), which was an even electron species that could follow the mobile proton dissociation pathway to produce b-type ions.
ECD spectra of the singly labeled Aβ 20 and Aβ 25 are shown in Figures 1b and and2b,2b, respectively. For Aβ 20 peptide, all z ions and the c9 ion displayed a ~104 Da mass shift from those produced in the ECD of its unmodified counterpart, but smaller c ions that do not contain the lysine residue showed no such mass shift; thus, the TMP tag was added to the lysine residue rather than at the N-terminus. Likewise, for Aβ 25 peptide, all fragment ions containing the lysine residue displayed the characteristic ~104 Da mass shift, while those without the lysine residue showed none, unambiguously locating the TMP tag at the side-chain of the lysine residue.
The addition of a single TMP tag appeared to greatly reduce the abundance of the backbone fragments, but not the number of cleavages. The intrinsic recombination energy of the pyridinium ion (4.71 eV)  is much greater than that of the N-terminus protonated peptide (3.71 eV) . After the initial electron capture in a high-lying Rydberg state, the pyridinium is far more likely to be the eventual neutralization site than the protonated N-terminal amino group. This resulted in the formation of a stable radical that was unlikely to undergo the typical c/z dissociations. However, it appeared that there was still a small but significant probability that the electron ended up at the N-terminus, leading to the observed N-Cαcleavages (vide infra).
Both the abundance and frequency of the backbone N-Cα cleavages were greatly reduced with the addition of a second TMP tag at the N-terminus (Figures 1c and and2c),2c), as one would expect from the dissociation-recapture mechanism, since both charges were “fixed”, and no H atom formation was initially expected upon electron capture. However, N-Cα cleavages were not completely eliminated from the ECD of these doubly tagged peptides, and there were also some H loss products present, albeit in much lower abundance. These H atoms were probably lost from the methyl groups on the pyridinium ring after it was neutralized, as shown in Scheme 2 leading to the formation of stable even electron species, which could not undergo further radical driven reactions. Since the recapture cross section of a free H atom by a gas phase peptide ion was very low, and the solvation of the TMP group by backbone carbonyls leading to the concerted H atom transfer from the methyl group to the carbonyl oxygen appeared unlikely, there must existed a second pathway to account for the observed c/z ions in the ECD spectra of these doubly labeled peptides.
One possibility is that the electron was first neutralized near the TMP moiety, and the resulting radical at the alpha carbon on the pyridine ring could abstract a hydrogen atom from a nearby (through space) amino acid residue side-chain beta carbon, generating a beta radical that could lead to c/z and a/x ion formations (Scheme 3). Free radical driven backbone cleavages have been reported by Beauchamp and coworkers in their free radical initiated peptide sequencing (FRIPS) studies , and were recently applied in the radical-directed dissociation of whole proteins in the gas phase . In this study, however, the initially produced alpha radical on the pyridine ring was supposed to be fairly stable and unlikely to propagate; more importantly, the FRIPS mechanism (Scheme 3) calls for the formation of c• ions and z•-H ions, while in the ECD spectra, only the even electron c ions and odd electron z• ions were observed. Thus, the FRIPS-like mechanism cannot account for all the backbone fragment ions observed here. A second possibility is that an amide superbase mechanism could be at work, where coulomb-assisted dissociative electron attachment at the backbone carbonyls generated an aminoketyl anion radical that abstracted a nearby proton to produce an aminoketyl radical that could undergo facile N-Cα bond cleavages. The proton most likely came from the methyl group on the pyridinium ring, as its acidity was increased by the positive charge on the nitrogen atom. Further experiments employing a deuterium labeled TMP tag would be helpful in determining the origin of the protons.
While the number of the fixed charge tags appeared to have a profound effect on the abundance and frequency of the backbone cleavages, the position of these tags seemed to have a less dramatic influence. For the doubly tagged Aβ20, either of the two TMP tags could be the neutralization site, or the site that provided the proton during ECD, as substantiated by the observation of the c3, c8 ions which must have retained the charge at the N-terminal TMP tag, and the z4, z7 ions which must have had the lysine side-chain TMP tag as the charge carrier (Figure 1c). For the doubly tagged Aβ25, the N-terminal TMP tag was a possible neutralization site as indicated by the presence of z8, and x8 ions (Figure 2c), but it was unclear if the tag on the lysine side-chain could also contribute to provide the proton necessary for backbone cleavages since all observed fragments contained the lysine residue. Moreover, the cleavages did not appear to be limited to regions that were adjacent to the charged sites in the sequence. This would certainly be true for remote charge assisted electron capture at backbone carbonyls, and it would also be expected if these cleavages were the results of the through-space radical propagation. Previously, cleavages occurring spatially but not necessarily sequentially close to the initially formed radical site have been observed .
The singly tagged peptides did show some differences in backbone cleavage abundances. When the tag was far away from the protonated site as in the case of the Aβ20 peptide, only moderate drops in z ion abundances were observed (Figures 1a, b). The c ions showed slightly more abundance decrease because their formations required the TMP tag site to be neutralized, which did not easily lead to N-Cα bond cleavages. For the Aβ25 peptide (Figures 2a, b), almost all fragment ions showed significant decrease in abundance in the ECD spectrum of the singly labeled peptide. This might be due to the close proximity of the protonated site and the TMP tagged site in the Aβ25 peptide, which would greatly reduce the probability that the electron capture occurred on the protonated N-terminal site. In addition, tag locations also seemed to influence the abundances of various side-chain loss and tag loss products (vide infra).
Aside from backbone cleavages, fragment ions that resulted from small molecule losses, single or multiple side-chain cleavages as well as a combination of backbone, side-chain cleavages and small molecule losses were also observed in the ECD spectra of all Amyloid β peptides studied here. These fragment ions were labeled in Figures 1 and and2,2, with their observed and theoretical masses listed in supplementary tables 1–6. All observed cleavages were also summarized in Figures 3 and and44.
It has been shown previously in a neutralization-reionization study of gas-phase pyridinium ion that the pyridinium radical preferentially lost the N-bound H or D atom to reform the aromatic ring , which competed favorably over the hydrogen rearrangement within the pyridinium ring. For the doubly TMP tagged peptides studied here, this implied that loss of the whole tag should be a favored process upon electron capture (Scheme 4). However, as can be seen from Figures 1c and and2c,2c, the tag loss peaks were much weaker (by as much as an order of magnitude in the latter case) than the corresponding peaks with loss of the tag and an additional methyl group. Scheme 5 represents two possible pathways to generate the tag loss product with the additional methyl loss, which led to the formation of a charged even electron species that was detected, and a stable radical species with the radical residing on the alpha carbon, which may also exist in several other possible resonance structures. Scheme 5a is a McLafferty rearrangement, which is both highly likely and a rearrangement with very low activation barrier.
Alternatively, the methyl group lost could come from elsewhere on the peptide such as the valine side-chain (scheme 5b). The loss of the TMP tag left the radical site on the ε-carbon of the lysine side-chain, which was an unconjugated primary radical, a fairly reactive species prone to further radical rearrangements. This radical may abstract a hydrogen atom from the alpha carbon of the valine residue, leading to the additional loss of methyl group (Scheme 5b). This mechanism was actually supported by the following observations. First of all, the relative abundance of the tag loss product with additional methyl group loss to that without was much higher for the doubly labeled Aβ 25 than the doubly labeled Aβ 20. Since the Aβ 25 has several leucine and isoleucine residues which could also lead to methyl loss from the tag loss product upon H atom abstraction from the alpha or beta carbon, this observation lends same support to the model in scheme 5b; whereas in the case of the Aβ 20, for this model to be correct, the H atom abstraction would have to take place at the alpha carbon of the single valine residue. Secondly and more importantly, fragment ions corresponding to additional loss of other alkyl groups such as the ethyl and propyl were only observed in ECD of the Aβ 25, corresponding to the presence of multiple leucine/isoleucine residues. Had Scheme 5a been the major pathway for the combined loss of tag and methyl groups, tag plus ethyl loss would only have been observed if the originally abstracted H atom was from the beta rather than the gamma carbon of the lysine side-chain.
For singly labeled peptides, the methyl loss peaks were much stronger than the tag loss peaks, particularly for the singly labeled Aβ 20, where it was the most abundant fragment ion (Figure 1b). The methyl group did not appear to come from the TMP tag, since the addition of a second tag greatly reduced the abundance of the methyl loss product for both peptides. Once again, the most likely source of the methyl group was the side-chain of the valine residue, where the initially formed radical could abstract a hydrogen atom from the alpha carbon of the valine residue, and the resultant alpha radical could lose one of the two methyl groups to form a stable even electron species (Scheme 6). Selectively deuterating the TMP tag or the valine residue would help to identify the source of the lost methyl group. For Aβ 25, the alpha radical on the one of the isoleucine residues or the beta radical on either the isoleucine or leucine residue could also lead to the loss of a methyl group (Scheme 6), although the methyl loss peak there was much weaker than in the ECD spectrum of the Aβ 20. This might be due to the different conformations of the two peptides, with the Aβ 20 having the valine residue closer to the TMP tag on lysine, and the Aβ 25 having the tag farther away from the isoleucine/leucine residues. Likewise, the dramatic abundance drop of the methyl loss product ions when a second TMP tag was added to the N-terminus may also be due to the conformational changes.
Small molecule and side-chain losses are common in ECD of multiply protonated peptides . The hydrogen atom generated from the neutralized protonated site plays an instrumental role in the proposed mechanism. Such was also the case for the ECD of the unlabeled peptides studied here, where ammonia and water losses as well as side-chain losses from serine, asparagine, lysine, isoleucine, leucine, and methionine residues were observed.
In a previous study, ECD of substance P modified with coumarin tags produced far more side-chain cleavages than the unmodified peptide, and the abundances of these side-chain cleavage products appeared to increase with the number of the tags . It was believed that the presence of radical traps inhibited the backbone cleavage pathways, thus redirecting the radical to the side-chains, possibly by changing the gas phase conformation of the peptide. A closer examination revealed that the great majority of the side-chain loss products from the ECD of the tagged substance P were also accompanied by tag loss. The (singly) lysine tagged substance P did produce some “pure” side-chain loss products, albeit in lower abundances. Similar trends were observed here, where most enhanced side-chain cleavages were primarily observed when they were also accompanied by tag loss. One notable difference is the abundant solo methyl loss peak observed in singly tagged Amyloid peptides and the doubly tagged Aβ20.
These trends can be explained by the number of available protonation sites, and the tag’s ability to stabilize a racial. For the singly tagged substance P, the likely charged sites were the arginine side-chain guanidine group and the remaining untagged amino group, which upon electron capture could produce the hydrogen atom initiating side-chain cleavages. For the doubly tagged substance P, one of the charge carriers was the protonated guanidine group, and the other most likely was the protonated amide nitrogen on the tagged site. The latter would be the favored neutralization site upon electron capture, which led to the loss of the neutral tag and left the radical site on the peptide lysine side-chain, capable of inducing secondary side-chain cleavages. As a result, for doubly tagged substance P, all observed side-chain cleavages were from the tag loss products .
Unlike the singly tagged substance P, all tagged Aβpeptides studied here contained at least one non-protonated charge carrier (the fixed charge tag), which also happened to be the preferred neutralization site due to its larger recombination energy. As discussed earlier, the electron capture at the TMP tag resulted in the loss of the neutral tag as a primary product (although not necessarily the most abundant product), which could undergo secondary side-chain losses as the radical site remaining on the peptide was a primary radical with relatively low stability (Scheme 4). Consequently, in the ECD spectra of the TMP tagged peptides, whether with one or two tags, most observed side-chain loss products were secondary fragment ions from the tag loss product, just like what have been observed in the ECD of the doubly tagged substance P. However, in the ECD spectra of singly labeled Aβpeptides, some side-chain losses without accompanying tag loss were also observed. These were often accompanied by NH3 loss instead, such as the -CH3-NH3 peaks in Figures 1b and and2b,2b, and the –NH3-CH2SCH3 peak in Figure 2b. Thus, the protonated N-terminal amino group may also be a possible neutralization site, even though it may not be the favored one, in accordance with the observation of multiple z ions in Figure 1b.
d and w ion formations resulting from secondary side-chain cleavages after the primary N-Cα bond cleavage were common in ECD of multiply protonated peptide ions. Their abundances were often dramatically increased with increased precursor ion internal energy, such as in hot ECD or AI-ECD, which was very useful in differentiating the isomeric leucine and isoleucine residues [24, 36]. Other types of secondary fragments requiring radical migration from the alpha carbon at the cleavage site prior to secondary side-chain cleavages have also been observed previously [13, 25]. For the unlabeled peptides studied here, many z ions experienced secondary side-chain cleavages (Figures 1a, ,2a2a and supplementary tables 1 and 4), but none of the c ions displayed any secondary side-chain losses, as the latter did not contain a radical site. Some secondary fragment ions resulted from loss of different groups from the same side-chain. Thus, the hydrogen atom abstracted did not appear to be limited to those on the backbone alpha carbons; some of the ions observed would require the hydrogen atom on the side-chain to be abstracted prior to secondary cleavages. For example, the z8 ion from the ECD of the Aβ25 peptide could lose either the even electron CH3-S-CH=CH2 molecule or the odd electron CH3-S-CH2• radical (Scheme 7a, b). Complete side-chain loss from the leucine or isoleucine residue was also apparent, which left the radical on the peptide backbone that could initiate further cleavages. This was evident in Figure 2a and supplementary table 4, where z8 ion with multiple side-chain losses was observed.
The ECD spectrum of the singly tagged Aβ20 peptide contained many similar secondary fragment ions as seen in that of the unlabeled peptide. These [z – R] ions (where R denotes a side-chain) were almost certain to result from the electron capture by the protonated N-terminal amino group, as the lysine TMP tag must retain its charge so that they could be detected. Furthermore, several methyl loss peaks from various z ions were present in the ECD spectrum of the singly labeled Aβ20 peptide, but were absent in that of the unlabeled peptide. No z ions smaller than z6 experienced the methyl loss, thus the methyl group most likely were lost from the valine side-chain, instead of from the TMP tag. It was unclear, however, why the presence of a TMP tag enhanced the methyl loss from both the charge reduced molecular ion and the primary z ions, as it did not appear to be directly involved (i.e. the methyl was unlikely to come from the TMP tag). For the singly tagged Aβ25 peptide, neither z ions nor secondary fragment ions from z ions were observed. This was probably due to the close proximity of the N-terminus and the TMP tag, which made the electron capture at the N-terminus less likely than when they were farther apart as in the case of the singly tagged Aβ20 peptide. However, extensive secondary fragmentation was observed on the molecular ion that had lost the neutral tag only or the neutral tag along with partial or full loss of the lysine side-chain (Figure 2b and Supplementary table 5), provided that the radical still resided within the peptide after the tag or lysine side-chain loss. ECD of both doubly tagged peptides produced plenty of secondary side-chain loss products after the initial tag or lysine side-chain loss, just like the singly tagged Aβ25 peptide. In absence of a protonated site, the electron capture was certain to take place at the TMP tagged site, generating a radical upon neutral tag loss, which can initiate further cleavages.
Finally, some internal fragments were observed with high mass accuracy in both the unlabeled and labeled peptides (Figures 1a, 2a-c, Supplementary tables 1, 4-6). These have not been previously reported, most likely because of the charge locations near the termini for substance P and the tryptic peptides commonly studied. The two peptides studied here have one of the charge carriers, the lysine residue, in the middle of the sequence, thus making possible the detection of internal fragment ions generated, particularly when the charge was fixed on the lysine residue. Their abundances were fairly low compared with those of the terminal fragment ions, probably because of the many other channels, such as the secondary side-chain loss channels, present that were more favorable due to low activation energies or less stringent conformational requirements. Nonetheless, the presence of these internal fragments demonstrated further that the free radical cascade mechanism could play an important role in the backbone cleavages during ECD of linear peptides as well.
The addition of fixed charge groups (TMP) significantly changed the ECD behavior of two amyloid β peptides. In general, a higher number of TMP tags correlated with fewer backbone cleavages and more abundant side-chain cleavages. The TMP tag was chosen because of its ability to stabilize (trap) the originally formed radical upon electron capture, as well as its non-protonated nature which was postulated to inhibit the hydrogen atom formation that was essential for the N-Cα bond cleavage in the dissociation-recapture mechanism. Although low abundance H loss products were observed in the ECD spectra of doubly tagged peptides, the H atoms generated there were not expected to play an important role in backbone cleavages due to the small cross section for its recapture by the peptide and the unlikelihood of the fixed charge site to form a hydrogen bond with backbone carbonyls to initiate concerted hydrogen atom transfer for N-Cα bond cleavages during ECD. Still, some c and z type ions were observed in the ECD of doubly tagged peptides, demonstrating that there existed other, non-H atom mediated, pathways for c/z ion formations in ECD, which may be radical driven, or resulted from the coulomb-assisted dissociative electron transfer. However, because the modified peptides often have very different electronic and conformational properties from the unmodified ones, these results did not necessarily undermine the importance of the hydrogen atom in the ECD of peptides. In fact, the opposite might be true as the doubly tagged peptides without a protonated site produced far fewer and less abundant backbone cleavages.
The apparent blocking of the backbone fragmentation channels seemed to open up new channels for side-chain cleavages, possibly as a result of the redirection of the radical site towards side-chains. Most side-chain cleavages from the TMP tagged Aβpeptides were accompanied by the tag loss. This reaffirmed that the charge neutralization predominantly occurred at the TMP tag, which could easily lose the tag and generate a primary radical that can initiate further side-chain cleavages. Secondary fragment ions were abundant in the ECD spectra of both Aβpeptides, with or without the TMP tags. Frequently, these ions were the results of secondary cleavages following through-space hydrogen atom abstraction. Future experiments employing selectively deuterated TMP tag or amino acid side-chains can help to explain different processes in the ECD of these modified peptides. Finally, several internal fragments were observed in the spectra, which provide strong support to the free radical cascade mechanism.
The authors gratefully acknowledge the financial support from the NIH/NCRR P41RR10888, NIH/NHLBI N01HV28178, NIH/NIGMS R01GM078293, MSD SCIEX, and ACS Petroleum Research Fund. They thank Dr. Raman Mathur, Dr. Vera B. Ivleva, Dr. Cheng Zhao, Dr. Chunxiang Yao, Dr. Michael Bowman, Konstantine Aizikov, and Nadezda Sargaeva for helpful discussions.
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