We used a different, more direct, method to probe the amyloid-β oligomerization process: ion mobility coupled with mass spectrometry13-15
. Details are given in the Methods section. Here the results for Aβ40 are given as an example. The mass spectrum of Aβ40 is shown in and arrival time distributions (ATDs) of the z
= −2 and −5/2 peaks (z
= total charge, n
= oligomer order) are given in , respectively, for both high and low injection energies. High-resolution 13
C isotope distribution measurements (insets in ) on the z
= −3 peak and z
= −2 peak indicate that the z
= −3 peak is caused by monomer (i.e. n
= 1, Δ(m
) = 0.33), whereas the z
= −2 peak results from both monomer (z
= −2, n
= 1, Δ(m
) = 0.5) and dimer (z
= −4, n
= 2, Δ(m
) = 0.25). The ATD of the z
= −2 peak () is bimodal (peaks at ~520 and ~660 μs), which indicates that at least two non-interconverting species exist on the timescale of the experiment, in agreement with the mass spectrum.
Negative-ion mass spectrum and ATDs of Aβ40
Injection-energy studies () unambiguously identified the 660 μs peak as the monomer (z = −2, n = 1) because it occurred only at high injection-energies, and thus resulted from oligomer dissociation, and because no additional peaks were observed at longer times. Only two peaks were observed in the ATD at lowest injection energy, so the peak at 520 μs can be assigned to the dimer (z = −4, n = 2). Similar injection energy studies on the z/n = −5/2 peak identified both a dimer with z = −5 and n = 2 at 100 eV injection energies and a tetramer with z = −10, n = 4 at 23 eV injection energies, although the resolution of the experiment was insufficient to observe a clean bimodal ATD. (This issue is dealt with in more detail in Supplementary Information for the z/n = −5/2 ATD of both Aβ40 and Aβ42. A peak-width analysis is given based on the diffusion equations for ions drifting in gases.) Hence, the Aβ40 solution dominantly contained monomer, dimer and tetramer, with no trimer and larger oligomers observed.
Similar experiments were carried out on the Pro19
(O) alloforms of Aβ40 and on the Met35
(O) alloform of Aβ42 (details are given in Supplementary Information). These systems were chosen because PICUP experiments have shown that both substitutions are known to either reduce or eliminate fibril formation16,17
and restrict oligomer production to relatively small sizes according to Klein et al.18
and Bitan et al.19
In all cases the largest oligomer observed was the tetramer. The ATDs for the z
= −5/2 peaks sprayed from solutions under identical conditions of all the systems considered here are summarized in . These data indicate that the ATD for Aβ42 is much more complex than that for the other five systems. Injection-energy studies15
indicate that the peak at the shortest times in the Aβ42 ATD is the dodecamer (Aβ42)12
, and that the complex multipeak feature at longer times results from the dimer, tetramer and hexamer (see detailed discussion in Supplementary Information
). We discuss this ATD shortly.
Ion mobility allows collision cross-sections (σ
) of each oligomer to be measured accurately20
(see Supplementary Information
for the measured cross-sections). A plot of σ
(Supplementary Information) has two important features. Firstly, for all systems, as n
decreases. This indicates that the apparent ‘size’ of each monomer unit within an oligomer decreases as oligomerization proceeds. This result is not unexpected, but emphasizes that oligomerization induces a certain amount of structural accommodation. One cause of this accommodation could be the self-selection of favoured structures as oligomerization proceeds. For example, both experiment and molecular dynamics modelling are consistent with a reasonably diverse ensemble of Aβ42 monomer structures in solution21
. Detailed analysis of the −5/2 ATD peak shapes of Aβ42 (Supplementary Fig. S4
) indicates that multiple structures are also present for dimers and tetramers of this alloform. However, the experimental linewidth significantly narrows for the Aβ42 hexamer and dodecamer, which suggests a single structure for these two important species.
The second feature in the σ
graph is that Aβ42 remains relatively larger (that is, accommodates less) than all other alloforms. These data are consistent with the results of intrinsic fluorescence studies22
, which showed that the structure of the centre (Leu17
) of Aβ42 was relatively stable compared with that of Aβ40. In addition, these data offer insight into why Aβ42 aggregation states and, by implication, the contribution of Aβ42 to the aetiology of Alzheimer’s disease are so different from those of other amyloid-β peptides. We obtained this insight by comparing measured cross-sections with those predicted by a simple structural model (for model details see Supplementary Information
In the model, the centre-to-centre distance (diameter) of an amyloid-β dimer constructed from quasispherical monomer units was adjusted to obtain the experimental dimer cross-section. This fitting accounts for a significant fraction of the monomer accommodation as n increases. Larger structures were then assembled using these calibrated dimer centre-to-centre distances. However, as mentioned above, a number of structures contribute to the experimental dimer cross-section, which indicates that the model cross-sections will be a bit too high when compared to oligomers of higher order and hence should be upper limits because no further accommodation is included. The results for Aβ42 given in are revealing. For example, the experimental tetramer cross-section falls between the model linear tetramer and a tetramer segment of the planar hexagon, and is much larger than the model planar square cross-section (more on this point shortly). The experimental hexamer cross-section is significantly smaller than the model linear cross-section and substantially larger than the closest-packed model cross-section, which rules these structures out. However, it is only moderately smaller than the model planar hexamer cross-section, a result consistent with the assumptions of the model and the tetramer structure, and so it supports this structure for (Aβ42)6. Similarly, the side-by-side planar hexagons can be ruled out as a structure for the dodecamer because their model cross-section is far larger than the experimental one, but the cross-section of the stacked hexagon model structure is in very good agreement with experiment. Hence, the experimental cross-sections are consistent with a quasiplanar hexagonal structure for the six-member ‘paranucleus’ and with stacked hexamers for the dodecamer.
Experimental and model cross-sections (Å2) for Aβ42 oligomers
An expanded version of the ATD for the z
= −5/2 of Aβ42 wild type is given in with the ‘structural’ assignments shown for the various peaks. There are two additional important features. Firstly, the ATD goes to the baseline where the octamer would appear. Hence, Aβ42 does not oligomerize via monomer or dimer addition past formation of the paranucleus (Aβ42)6
, which suggests the mechanism in occurs. Apparently, the structural stability of the paranucleus ring greatly reduces the monomer (dimer) addition rate as it accommodates homotypical growth. This critical feature indicates the potential importance of paranuclei in the aetiology of Alzheimer’s disease10
The second important feature in the Aβ42 ATD in relates to the complete absence of any signal at arrival times prior to that of dodecamer. This is unusual because, in most instances, a sloping ATD that extends to earlier times is observed, which indicates the presence of larger oligomers that are not well resolved. The absence of ion signal at these earlier times is consistent with the absence of octadecamers (18-mers) and indicates a lack of monomer or dimer addition to the dodecamer. The absence of an 18-mer that corresponds to ((Aβ42)6
strongly suggests that addition of the third paranucleus is slow, and leads to accumulation of ((Aβ42)6
. The reason aggregation of Aβ42 stops at the ((Aβ42)6
dodecamer is not clear. Two plausible mechanisms are discussed in the Supplementary Information24,25
. Both mechanisms rationalize why the addition of a third hexamer is energetically unlikely and leads to a long-lived, but metastable, dodecamer. Apparently, this dodecamer eventually rearranges and rapidly adds monomer and forms fibrils. That Aβ42 clogged the nanospray tips used to spray the sample solution (that is, rapidly formed very large oligomers and/or fibrils), whereas each of the other five systems reported here (see ) sprayed beautifully for a minimum of several days up to more than a week without the tip clogging supports the rearrangement hypothesis. Aggregates of higher order (Aβ42)n
would rapidly move out of the mobility–mass range of the ion mass spectroscopy instrument and their dispersal would make them difficult to detect with the limited sensitivity of this instrument.
To test this aggregation hypothesis we looked at the Aβ42 positive-ion mass spectrum on a Q-TOF instrument specially built to observe high-mass aggregates under conditions in which Aβ42 aggregation is maximized (see Supplementary Fig. S6
. A mound of ion intensity was observed that stretches from less than m
1,000 to m
8,000 and reflects a nearly continuous array of highly charged oligomers. Two sharp features at low m
were identified as +4 and +3 residual monomers. This assignment was confirmed by tandem mass spectroscopy (MS/MS) (Supplementary Fig. S6
inset). The MS/MS result indicated that monomer loss dominated the dissociation process, which is common for collisional dissociation of large aggregates28
. When Pro19
Aβ42 was sprayed under identical conditions, a very clean monomer-dominated spectrum was observed (Supplementary Fig. S6
), consistent with the fact that this alloform does not form fibrils17
A clue as to why Aβ42, but none of the other five systems, forms paranuclei is found in the relative cross-sections of the tetramers. This effect can be quantified using the model developed here. Each of the systems studied terminates at the tetramer, except Aβ42. A normalized plot of the size of each tetramer experimental cross-section relative to several possible tetramer model structures is given in . The model cross-section for the linear tetramer was taken as the benchmark because it is the largest possible structure and all system sizes were normalized to that value. The results indicate that the Aβ42 tetramer is much more ‘open’ than Aβ40 or the other three alloforms shown. If the experimental cross-sections are fitted to a dimer–dimer angle the structures in are obtained.
The normalized cross-sections for the tetramers
Another dimer could easily add to the ‘open’ Aβ42 tetramer structure () to form the quasiplanar hexamer paranucleus (or a monomer could add to form a pentamer, which explains the stacked dipentamer shown in ). However, the ‘closed’ Aβ40 tetramers in (and other alloforms) are not structurally disposed to the addition of either a monomer or a dimer and hence they form stable, long-lived tetramers. Our experimental data show the structure of the tetramer to be crucial in determining whether an amyloid-β alloform goes on to form paranuclei and dodecamers and subsequently contributes to the aetiology of Alzheimer’s disease. Hence the (perhaps small) folding differences in the various monomers are amplified by aggregation, and at the tetramer dramatic differences occur. From a different perspective, the ‘dimer–dimer’ interface is different from the ‘monomer–monomer’ interface, and perhaps the Aβ42 dimer is uniquely suited to form an open tetramer and the other systems are not. The tetramer is small enough to hope that serious modelling can be done to extract the factors at the molecular level in these systems that drive such crucial structural differences. These studies are underway.
A global scheme of amyloid-β oligomerization can be deduced by combining the data presented here with previous published data9,10
(). For Aβ42 a receptive structure in the tetramer allows further dimer addition and paranucleus formation with a planar hexagonal structure. Two paranuclei combine to form a stacked paranuclear dimer, which resists further transformation. Eventually, ((Aβ42)6
rearranges to form a new structure to which monomer rapidly adds to form large β-sheet oligomer assemblies. Aβ40, however, forms a more compact tetramer that firmly resists further addition and hence forms no paranuclei. A similar fate to that of Aβ40 befalls the Pro19
(O) alloforms of both Aβ42 and Aβ40. Although some of these systems eventually do form fibrils, they appear to do so by a mechanism that bypasses paranucleus formation10
Mechanism of oligomerization and eventual fibril formation for Aβ42 and for Aβ40
In related work Barghorn et al.29
isolated a species they called ‘globulomer’ from Aβ42 using a quite complex protocol. This species is soluble and has a molecular weight between 60 and 100 kDa. It is stable against dissociation for several days and only slowly self-aggregates to form larger oligomers in the absence of Aβ42 monomer. Application of proteases truncated the N-terminus of the globulomer Aβ42 monomer constituents up to about residue F20, which indicates that the C-terminal hydrophobic residues are in the centre of the globulomer. This result is consistent with our view of both the hexamer and the dodecamer complexes, in which the hydrophobic tails are envisioned as occupying the centre of the structures (see Supplementary Fig. S4
and the cartoon in Baumketner et al.21
). Barghorn et al.
suggest the globulomer is made up of 12 Aβ42 molecules, but their evidence for this is not conclusive29
.They also assume that the globulomer is formed by an independent mechanism than through Aβ42 fibrils, a suggestion at odds with the mechanism we give in and one that would be difficult to rationalize with a kinetic model (which they did not present).
One additional important point is worth making. Lesné et al.6
used amyloid precursor protein transgenic Tg2576 mice to demonstrate that memory defects occur in ‘middle-aged’ mice (6–14 months) without neuronal loss, but in older mice abundant neuritic plaques that contain Aβ42 were observed. What they observed in these middle-aged mice was an extracellular accumulation of a ~56 kDa soluble amyloid assembly, Aβ*56. These authors proposed that this 56 kDa assembly impairs memory by an unknown mechanism independent of either plaque formation or neuronal loss. Their observations are supported by recent results of Cheng et al.5
, who also used transgenic mice and the ‘Arctic’ (E22G) mutant alloform of Aβ42, which implicate Aβ*56 rather than fibrils as a determinant of Alzheimer’s disease. Here we show that Aβ42 forms in vitro
a dodecamer composed of stacked hexamer paranuclei. This dodecamer is the terminal species observed in our experiments, and has a mass of ~55.2 kDa, which suggests it is the soluble assembly that Lesné et al.
. This assembly has not yet rearranged into a β-sheet structure and may possibly be the key neurotoxic assembly in Alzheimer’s disease.