Methods For Preventing And Treating Alzheimer's Disease (ad)

Abstract

The present invention relates to methods for preventing Alzheimer's disease (AD) with an A.beta.42 mimotope and binds to an antibody specific for DAEFRH (SEQ ID NO: 1) which is a part of the naturally-occurring A.beta.42 sequence.

Description

[0001] The present invention relates to methods for preventing and treating Alzheimer's disease (AD).

[0002] Amyloid-.beta. peptide (A.beta.) plays a central role in the neuropathology of Alzheimer's disease (AD) (Roher et al 1993: ".beta.-Amyloid-(1-42) is a major component of cerebrovascular amyloid deposits: Implications for the pathology of Alzheimer disease" PNAS 90:10836). Familial forms of the disease have been linked to mutations in the amyloid precursor protein (APP) and the presenilin genes. Disease-linked mutations in these genes result in increased production of the 42-amino acid form of the peptide (A.beta.42), which is the predominant form found in the amyloid plaques of Alzheimer's disease. An animal model for the disease is commercially available. The PDAPP transgenic mouse, which over-expresses mutant human APP (in which the amino acid at position 717 is F instead of V), progressively develops many of the neuropathological hallmarks of Alzheimer's disease in an age- and brain-dependent manner (Games et al 1995: "Alzheimer-type neuropathology in transgenic mice overexpressing V717F .beta.-amyloid precursor protein" Nature 373:523).

[0003] Vaccination studies with a "normal", not mimotope-based vaccine have already been performed. Transgenic animals were immunized with aggregated A.beta.42, either before the onset of AD-type neuropathologies (6 weeks) or at an older age (11 months): Immunization of young animals prevented the development of plaque formation, neuritic dystrophy and astrogliosis. Treatment of older animals markedly reduced AD-like neuropathologies. This experimental vaccination approach induced the development of antibodies against A.beta.42 able to cross the blood-brain barrier and attack amyloid plaques (Schenk et al 1999: "Immunization with amyloid-.beta. attenuates Alzheimer-disease-like pathology in the PD-APP mouse" Nature 400:173). The plaques are subsequently removed by several mechanisms, including Fc-receptor mediated phagocytosis (Bard et al 2000: "Peripherally administered antibodies against amyloid .beta.-peptide enter the central nervous system and reduce pathology in a mouse model of Alzheimer disease" Nature Med 6:916). This vaccine was also able to delay memory deficits (Janus et al 2000: "A.beta. peptide immunization reduces behavioural impairment and plaques in a model of Alzheimer's disease" Nature 408:979).

[0004] A highly promising immunization therapy for AD has been in clinical trials since late 1999. Immunization is presumed to trigger the immune system to attack the plaques and clear these deposits from the affected human brain, although the precise mechanism underlying needs to be characterized in more detail.

[0005] These clinical trials were conducted by the pharmaceutical company Elan in conjunction with its corporate partner, American Home Products (therapeutic vaccine AN-1792, QS21 as adjuvant). Phase I trials were successfully completed in 2000. Phase II trials were begun late 2001 to test efficacy in a panel of patients with mild to moderate AD.

[0006] Now these phase II trials have been permanently discontinued due to neuroinflammation in several patients (Editorial 2002 "Insoluble problem?" Nature Med 8:191). The symptoms included aseptic meningoencephalitis leading to the immediate halt of these world-wide trials. In the worst case scenario, affected patients will be shown to have mounted an autoimmune response--a risk inherent in many immunotherapies. Autoimmune complications could have been anticipated given the ubiquity of APP, which of course bears antigenic determinants in common with its proteolytic product. More recently, additional studies concentrated on the nature of aggregated A.beta.42 immunization-induced antibodies (in humans and mice) revealing that most antibodies recognize a small domain between amino acid 4 and 10 of A.beta.42 (A.beta.4-10). The mouse antibodies were able to block A.beta. fibrillogenesis and disrupted pre-existing A.beta. fibers (McLaurin et al 2002: "Therapeutically effective antibodies against amyloid-.beta. peptide target amyloid-.beta. residues 4-10 and inhibit cytotoxicity and fibrillogenesis" Nature Med 8:1263). Of note, the human antibodies do not react with APP exposed on the surface of cells or any other non-aggregated proteolytic product of the precursor (Hock et al 2002: "Generation of antibodies specific for I-amyloid by vaccination of patients with Alzheimer disease" Nature Med 8:1270). A clear difference was observed between human and mouse sera: In contrast to human antibodies, mouse antibodies detect monomeric, oligomeric, and fibrillar A.beta.. This is of importance and may be a prerequisite for the therapeutic potency since evidence is accumulating that small oligomers of A.beta., which are not recognized by human anti-A.beta., are the major toxic players in the disease (Walsh et al 2002: "Naturally secreted oligomers of amyloid .beta. protein potently inhibit hippocampal long-term potentiation in vivo" Nature 416:535). Thus, a potential new strategy is the immunization with a vaccine containing .beta.-amyloid amino acids 4-10 (instead of aggregated A.beta.42). Despite unknown efficacy this strategy may also face autoimmune problems since patients shall be directly immunized with a (linear B cell) "self" epitope.

[0007] Despite these disappointing developments in recent AD vaccination strategies, an A.beta. vaccine is still regarded as the most promising way for combatting AD. However, there is an urgent need for improvements and new strategies in AD vaccination. Especially, such a vaccine should not induce autoreactive T and/or B cells.

[0008] Therefore, the present invention provides the use of a compound comprising the following amino acid sequence

X.sub.1X.sub.2X.sub.3X.sub.4X.sub.5X.sub.6,

wherein X.sub.1 is an amino acid, except of C, X.sub.2 is an amino acid, except of C, X.sub.3 is an amino acid, except of C, X.sub.4 is an amino acid, except of C, X.sub.5 is an amino acid, except of C, X.sub.6 is an amino acid, except of C, and wherein X.sub.1X.sub.2X.sub.3X.sub.4X.sub.6X.sub.6 is not DAEFRH, said compound having a binding capacity to an antibody being specific for the natural N-terminal A.beta.42 sequence DAEFRH, and 5-mers thereof having a binding capacity to said antibody being specific for the natural N-terminal A.beta.42 sequence DAEFRH, for the preparation of a vaccine for Alzheimer's disease (AD).

[0009] According to the present invention an A.beta.42 mimotope is used for vaccination against AD: The mimotope induces the production of antibodies against A.beta.42 but not against the native APP. The mimotope may be identified with a (monoclonal) antibody and (commercially available) peptide libraries (e.g. according to Reineke et al. 2002: "Identification of distinct antibody epitopes and mimotopes from a peptide array of 5520 randomly generated sequences" J Immunol Methods 267:37). A (monoclonal) antibody is used that does not recognize APP but detects only different A.beta. species with amino-terminal aspartic acid (an example for such an antibody is described in Johnson-Wood et al 1997: "Amyloid precursor protein processing and A.beta.42 deposition in a transgenic mouse model of Alzheimer disease" PNAS 94:1550). Such an antibody has been proven to be an ideal tool to identify vaccine-suitable mimotopes in the course of the present invention. Although such monoclonal antibodies were shown to have beneficial effects in a mouse model of AD when directly administered to mice (Bard et al 2000: "Peripherally administered antibodies against amyloid 13-peptide enter the central nervous system and reduce pathology in a mouse model of Alzheimer disease" Nature Med 6:916), these antibodies have never been proposed to be used as mimotope search tools for isolating AD vaccine compounds.

[0010] In the prior art, all efforts were concentrated on the naturally occurring A.beta. peptide. As mentioned above, A.beta. peptide vaccine clinical trials were stopped due to neuroinflammation events. Indeed, T cell epitope prediction programs (BIMAS for class I-restricted epitopes and TEPITOPE for class II-restricted epitopes) propose high score (self) epitopes within the sequence. This could imply that the neuroinflammatory events are due to autoimmune reactions which would make such a vaccine unsuitable for a general application.

[0011] In contrast to such A.beta. vaccines proposed by the prior art, no autoimmune reactions are expected to occur during treatment with a vaccine containing a mimotope according to the present invention, because the (monoclonal) antibody used for mimotope identification according to the present invention does not recognize APP and the mimotope sequence is different from A.beta.42-derived self sequences that have been used in trials so far or shall be used in future trials.

[0012] The antibody used for the mimotope identification according to the present invention detects the A.beta.-derived amino acid sequence DAEFRH (=original epitope) with a free amino terminal aspartic acid, thus it does not recognize native APP. The antibody may be a monoclonal or polyclonal antibody preparation or any antibody part or derivative thereof, the only prerequisite is that the antibody molecule specifically recognises the DAEFRH epitope, i.e. that it does not bind to the natural N-terminally prolonged forms of the amyloid precursor protein, which means that the binding capacity to the DAEFRH epitope is at least 100 times, preferably at least 1000 times, more preferred at least 10.sup.5 times, higher than to the APP molecule. The antibody may be an antibody showing the same or a higher binding capacity to the DAEFRH sequence as the antibody described by Johnson-Wood et al., 1997. Of course, also antibodies with a lower binding capacity may be used (>10%, >50% or >80% of the binding capacity of the Johnson-Wood et al. antibody), although the higher binding capacity is more preferred.

[0013] The compounds according to the present invention bind to those antibodies with comparable specificity as the DAEFRH sequence.

[0014] Preferably, the compound to be used according to the present invention comprises or is consisting of a peptide, wherein

X.sub.1 is G or an amino acid with a hydroxy group or a negatively charged amino acid, preferably E, Y, S or D, X.sub.2 is a hydrophobic amino acid or a positively charged amino acid, preferably I, L, V, K, W, R, Y, F or A, X.sub.3 is a negatively charged amino acid, preferably D or E, X.sub.4 is an aromatic amino acid or L, preferably Y, F or L, X.sub.5 is H, K, Y, F or R, preferably H, F or R, and X.sub.6 is S, T, N, Q, D, E, R, I, K, Y, or G, preferably T, N, D, R, I or G, especially EIDYHR, ELDYHR, EVDYHR, DIDYHR, DLDYHR, DVDYHR, DIDYRR, DLDYRR, DVDYRR, DKELRI, DWELRI, YREFRI, YAEFRG, EAEFRG, DYEFRG, ELEFRG, DRELRI, DKELKI, DRELKI, GREFRN, EYEFRG, DWEFRDA, SWEFRT, DKELR or SFEFRG.

[0015] The compound (mimotope) according to the present invention has a preferred length of 5 to 15 amino acids. This compound may be provided in the vaccine in isolated (peptide) form or may be coupled or complexed to other molecules, such as pharmaceutical carrier substances or polypeptide, lipid or carbohydrate structures. Preferably, the mimotopes according to the present invention have a (minimum) length of between 5 and 15, 6 and 12 amino acid residues, specifically between 9 and 11. The mimotopes can, however, be coupled (covalently or non-covalent) to unspecific linkers or carriers, especially peptide linkers or protein carriers. Furthermore, the peptide linkers or protein carriers might consist of or contain T-cell helper epitopes.

[0016] Preferably, the pharmaceutically acceptable carrier is KLH, tetanus toxoid, albumin binding protein, bovine serum albumin, a dendrimer (MAP; Biol. Chem. 358:581) as well as the adjuvant substances described in Singh et al., Nat. Biotech. 17 (1999), 1075-1081 (specifically those in table 1 of this document) and O'Hagan et al., Nature Reviews, Drug Discovery 2(9)(2003), 727-735 (specifically the innate immune-potentiating compounds and the delivery systems described therein), or mixtures thereof. In addition, the vaccine composition may contain aluminium hydroxyde.

[0017] A vaccine comprising the present compound (mimotope) and the pharmaceutically acceptable carrier may be administered by any suitable application mode, e.g. i.v., i.p., i.m., intranasal, oral, subcutaneous, etc. and in any suitable delivery device (O'Hagan et al., Nature Reviews, Drug Discovery 2(9)(2003), 727-735). Typically, the vaccine contains the compound according to the present invention in an amount of 0.1 ng to 10 mg, preferably 10 ng to 1 mg, especially 100 ng to 100 .mu.g or, alternatively e.g. 100 fmole to 10 .mu.mole, preferably 10 pmole to 1 .mu.mole, especially 100 pmole to 100 nmole. The vaccine may also comprise typical auxiliary substances, e.g. buffers, stabilizers, etc.

[0018] According to another aspect, the present invention further relates to a method for isolating a compound binding to an antibody being specific for the natural N-terminal A.beta.42 sequence DAEFRH comprising the steps of [0019] providing a peptide compound library comprising peptides containing the following amino acid sequence

[0019] X.sub.1X.sub.2X.sub.3X.sub.4X.sub.5X.sub.6,

wherein X.sub.1 is an amino acid, except of C, X.sub.2 is an amino acid, except of C, X.sub.3 is an amino acid, except of C, X.sub.4 is an amino acid, except of C, X.sub.5 is an amino acid, except of C, X.sub.6 is an amino acid, except of C, and wherein X.sub.1X.sub.2X.sub.3X.sub.4X.sub.5X.sub.6 is not DAEFRH, [0020] contacting said peptide library with said antibody and [0021] isolating those members of the peptide library which bind to said antibody.

[0022] According to a specific embodiment of this aspect, the present invention relates to a method for isolating a compound binding to an antibody being specific for the natural N-terminal A.beta.42 sequence DAEFRH comprising the steps of [0023] providing a peptide compound library comprising peptides containing the following amino acid sequence

[0023] X.sub.1X.sub.2X.sub.3X.sub.4X.sub.5X.sub.6,

wherein X.sub.1 is a natural amino acid, except of K and C, X.sub.2 is a natural amino acid, except of C, X.sub.3 is a natural amino acid, except of K and C, X.sub.4 is a natural amino acid, except of K and C, X.sub.5 is a natural amino acid, except of C, X.sub.6 is a natural amino acid, except of P and C, and wherein X.sub.1X.sub.2X.sub.3X.sub.4X.sub.5X.sub.6 is not DAEFRH, [0024] contacting said peptide library with said antibody and [0025] isolating those members of the peptide library which bind to said antibody.

[0026] Isolating suitable 5-mers according to the present invention can be achieved in the way described above, adapted to libraries with 5 amino acid variables, and may preferably be performed either by screening a library having amino acid variables X.sub.1 to X.sub.5 as described herein or by identifying suitable 5-mers in a positive member screened in a 6-mer-library (see: above). In the same way, also 7-mer, 8-mer, 9-mer, 10-mer, libraries may be applied accordingly to screen for suitable sequences which bind to the present antibody-type. Suitable antibody-binding fragments of such longer sequences can be found, e.g. by testing these fragments with a length of 5, 6, 7, 8, 9, . . . amino acid residues for binding to the present antibody.

[0027] Such a method has been proven to be successful for providing A.beta. mimotopes according to the present invention.

[0028] Preferably, said peptides are provided in individualised form in said library, especially immobilised on a solid surface, such as e.g. possible with the MULTIPIN.TM. peptide technology. The library may also be provided as a peptide mixture and the antibody:peptide complexes may be isolated after antibody binding. Alternatively, the antibody may be immobilised and the peptide library (in suspension or solution) is then contacted with the immobilised antibodies.

[0029] Preferably, the screening antibodies (or the members of the peptide library) comprise a suitable marker which allows the detection or isolation of the antibody or the antibody:peptide complex when bound to a peptide of the library. Suitable marker systems (i.a. biotinylation, fluorescence, radioactivity, magnetic markers, colour developing markers, secondary antibodies) are readily available to the skilled man in the art.

[0030] The library has to be constructed to exclude the naturally occurring A.beta. sequence (e.g. DAEFRH), since vaccination with this sequence is clearly excluded from this invention.

[0031] A further suitable technique for isolating the epitopes according to the present invention is screening in phage-peptide libraries as e.g. described in WO 03/020750.

[0032] The present invention also relates to a composition comprising an anti N-terminal A.beta.42-antibody-binding peptide (or, in certain cases preferred, a larger molecule comprising such a peptide (e.g. the peptide linked to a carrier or delivery molecule)) as defined herein (optionally as single effective component), preferably to a vaccine against Alzheimer's Disease comprising such an antigen, especially an antigen which includes at least one peptide selected from the group EIDYHR, ELDYHR, EVDYHR, DIDYHR, DLDYHR, DVDYHR, DIDYRR, DLDYRR, DVDYRR, DKELRI, DWELRI, YREFRI, YAEFRG, EAEFRG, DYEFRG, ELEFRG, DRELRI, DKELKI, DRELKI, GREFRN, EYEFRG, DWEFRDA, SWEFRT, DKELR or SFEFRG. These peptides are--besides the other peptides provided with the present invention specifically suited to be used for the preparation of a pharmaceutical composition, especially for AD vaccines. These sequences are purely artificial A.beta.-mimotopes. The peptides may--for vaccination purposes--be coupled (covalently or non-covalently) to suitable carriers and may be provided as peptide compounds or complexes together with other compounds or moieties, e.g. adjuvants, peptide or protein carriers, etc. and administered in a suitable manner (as e.g. described in O'Hagan et al., Nature Reviews, Drug Discovery 2(9)(2003), 727-735).

[0033] The invention is further described in the following examples and the drawing figures, of course without being restricted thereto.

[0034] FIG. 1 shows the individualised peptide members of library 4 used for the present screening process.

[0035] FIG. 2 shows an inhibition assay with mimotopes for DAEFRH.

[0036] FIG. 3 shows another inhibition assay with other mimotopes for DAEFRH.

[0037] FIGS. 4 and 5 describe the results of inhibition assays performed with mimotope peptides according to the present invention

EXAMPLES

1. Generation of Monoclonal Antibodies (mAb) to Detect A.beta.42-Derived Peptide Species with Free N-Terminus (Free Aspartic Acid at the N-Terminus)

[0038] Mice are vaccinated with the 6mer peptide DAEFRH (natural N-terminal A.beta.42 sequence) linked to the protein bovine serum albumin BSA (to make use of the hapten-carrier-effect), emulsified in CFA (first injection) and IFA (booster injections). DAEFRH-peptide-specific, antibody-producing hybridomas are detected by ELISA (DAEFRH-peptide-coated ELISA plates). Peptide SEVKMDAEFRH (natural N-terminally prolonged sequence, APP-derived, containing the A.beta.42-derived sequence DAEFRH) is used as negative control peptide: hybridomas recognizing the prolonged peptide are excluded because they do not distinguish between A.beta.42-derived peptides with free aspartic acid at the N-terminus and APP-derived peptide DAEFRH without free aspartic acid.

2. Construction of Peptide Libraries

[0039] The mimotopes of the present invention have been found by adapting the method of Reinke et al., 2000, by screening peptide libraries for binding to an antibody (preferably a monoclonal antibody) which is specific for A.beta. species with amino-terminal aspartic acid. Another method is commercially available as MULTIPIN.TM. peptide technology.

[0040] The Multipin.TM. peptide technology involves synthesizing peptides on to specially prepared polyethylene pins mounted on blocks in a format which is compatible with the standard 8.times.12 microtiter plate used for many biological assays. Both pin-bound (non-cleavable peptides which remain covalently bound to the pin) and solution phase peptides (those that have been cleaved off the pin surface) can be produced by this method. PepSets, based on the Multipin synthesis system, permit the simultaneous synthesis and screening of large numbers of peptides.

[0041] PepSets consist of blocks of 96 individually synthesized peptides, two of which are carefully selected control sequences. Cleaved controls are assessed for purity by reverse phase HPLC and peptide content quantitated by amino acid analysis. Positive and negative non-cleavable controls are assessed by standard ELISA techniques.

[0042] PepSet peptides are available with a variety of chemical modifications including acetylation, biotinylation, phosphorylation and cyclization. The solution phase (cleaved) peptides are shipped as lyophilized powders.

[0043] For the production of solution phase peptides there is a choice of C-terminal endings, including acid and amide, depending on the intended peptide application. The cleavable bond is incorporated onto the pin surface, either as a preformed ester derivative of the C-terminal amino acid, or onto the "Rink" amide linker. Peptides with acid or amide end groups are then released by treating the pin-bound peptide with strong acid. Options for the scale of synthesis are a nominal 1 micromole or 5 micromole scale. Factors such as hydrophobicity and cleavage efficiency will affect peptide recovery, such that the expected yield of peptide is 0.5 to 1 micromole (around 1 mg of a 15mer peptide) when the peptides are synthesized on the nominal 1 micromole scale, or a yield of 2.5 to 5 micromole for peptides synthesized on the nominal 5 micromole scale.

[0044] Non-cleavable peptides remain covalently bound to the pins and can be used to rapidly screen for peptides of interest using ELISA techniques. Such peptides are useful for the purposes of antibody epitope scanning and structure-activity relationship (SAR) studies. Removal of bound antibodies or other proteins regenerates the peptides and allows their reuse in further assays. PepSets are used for a variety of applications including the identification of peptide leads of biological interest from scanning through protein sequences, the optimization of peptide leads, and the development of new generations of analogs. Flexibility in terms of the overall strategy used in screening procedures is greatly enhanced through the use of a variety of synthesis designs which together provide a systematic method to fully characterize the lead candidate.

[0045] The comprehensive results obtained from systematic peptide sets not only identify peptides of interest, but also indicates critical residues, their replaceability and optimal peptide length. Consequently, a range of related peptides may be ranked as a result of such findings. Replacement of L-amino acids with D-amino acids and other unusual residues is a powerful approach to manipulate the structure and conformation of a peptide. This method is also a rapid way to discover new analogs with different pharmacological properties, such as antagonists and peptides with increased stability.

[0046] Starting with a known protein sequence, all sequential antibody epitopes can be mapped using the Multipin approach. Several alternative procedures for mapping sequential B-cell epitopes are now possible. These include pin-bound peptides, solution phase peptides coated directly onto microtiter plates, and biotinylated peptides captured on microtiter plates previously coated with avidin or streptavidin.

[0047] For the present examples, the antibody described in example 1 is used for screening peptide libraries, however, any antibody preparation specifically recognizing the DAEFRH-sequence, but not the naturally N-terminally prolonged sequence of the A.beta. molecule (e.g. MDAEFRH, KMDAEFRH, SEVKMDAEFRH or the complete amyloid (precursor) protein, APP), such as e.g. described by Johnson-Wood et al., 1997.

[0048] Four libraries have been constructed for this purpose:

2.1. Library 1: This 6mer library contains peptides with the following sequences (amino acid positions 1 to 6): Position 1: all natural aa except of D, K, and C (17 possibilities Position 2: all natural aa except of A, K, and C (17 possibilities) Position 3: all natural aa except of E, K, and C (17 possibilities) Position 4: all natural aa except of F, K, and C (17 possibilities) Position 5: all natural aa except of R, K, and C (17 possibilities) Position 6: all natural aa except of H, K, C, and P (16 possibilities)

[0049] Library 1 is a mixture of hexapeptides. Theoretically, all possible peptides containing 17 different amino acids (see below) are included. The mixture does not contain any lysine and cysteine residue. Furthermore, the mixture does not contain:

aspartic acid at the specific position 1, alanine at the specific position 2, glutamic acid at the specific position 3, phenylalanine at the specific position 4, arginine at the specific position 5, and histidine at the specific position 6.

[0050] The synthesis is performed on an Applied Biosystems 431A-Synthesizer following the FastMoc protocol, with a synthesis scale of 0.25 mmol.

[0051] The synthesis starts with weighing 1 mmol of all desired amino acids (amino groups and side chains protected). Then, a mixture of Asn, Gln, Gly, Ile, Leu, Met, Pro, Ser, Thr, Trp, Tyr, Val was produced. Position-specific, the following amino acids are added:

Ala, Glu, Phe, Arg, His (position/mixture 1), Asp, Glu, Phe, Arg, His (position/mixture 2), Asp, Ala, Phe, Arg, His (position/mixture 3), Asp, Ala, Glu, Arg, His (position/mixture 4), Asp, Ala, Glu, Phe, His (position/mixture 5), and Asp, Ala, Glu, Phe, Arg (position/mixture 6, without Pro).

[0052] Mixture 6 was used to load the resin (2-chloro-tritylchloride resin, 1.49 mmol/g, Alexis Germany):

1 mmol amino acid residue mixture 6 611 mg resin (=0.91 mmol reactive groups) 15 ml dichloromethane 5.5 equivalent=5 mmol diisopropylethylamine (871 .mu.l).

[0053] The mixture is shaken in a flask for 1 h. Then, 1 ml methanol is added and the mixture is shaken for an additional 10 min. The loaded resin is extracted via a frit and washed twice with dimethylformamide, dichlormethane, isopropanol, methanol, and ether (30 ml of each). The drying is performed overnight in a high vacuum. The weigh-out quantity is 737 mg.

[0054] An aliquot of 5.66 mg is treated for 30 min with 1 ml of 20% piperidine in DMF to define the density of the resin. Then, the mixture is centrifuged. The free Fmoc protective group is photometrically measured in the supernatant (301 nm, coefficient of extinction=7800 M (e-1)). Accordingly, the density of the resin is 0.49 mmol/g.

[0055] All following steps are performed at the synthesizer, using the other mixtures (put in 5 different cartridges). 515 mg of loaded resin are used (corresponding to 0.25 mmol: amino acid mixtures are used in 4-times excess). The N-terminal Fmoc protective group is cleaved at the end of the synthesis. After washing with ethanol and drying overnight, cleavage of the peptides from the resin is accomplished by TFA/H.sub.2O (95:5, v:v). The TFA solution is concentrated in a Speed Vac to 1/5 volume and precipitated and washed in diethylether and lyophilized.

[0056] The 6mer peptides EIDYHR, ELDYHR, and EVDYHR are examples for mimotopes that can be detected by the monoclonal antibody produced according to example 1 above.

2.2. Library 2: This 6mer library contains peptides with the following sequences (amino acid positions 1 to 6): Position 1: D (fixed) Position 2: all natural aa except of A, K, and C (17 possibilities) Position 3: all natural aa except of E, K, and C (17 possibilities) Position 4: all natural aa except of F, K, and C (17 possibilities) Position 5: all natural aa except of R, K, and C (17 possibilities) Position 6: all natural aa except of H, K, C, and P (16 possibilities).

[0057] Peptide library 2 was constructed according to the method described above (under 2.1) for library 1.

[0058] The 6mer peptides DIDYHR, DLDYHR, and DVDYHR are examples for mimotopes that can be detected by the monoclonal antibody produced according to 1 above.

2.3. Library 3: A third peptide library is used in an additional approach to define mimotope sequences. This library contains the original sequence, and allows the detection of mimotopes more closely related to the original epitope.

[0059] This 6mer library contains peptides with the following sequences (amino acid positions 1 to 6):

Position 1: all natural aa except of K, and C (18 possibilities) Position 2: all natural aa except of K, and C (18 possibilities) Position 3: all natural aa except of K, and C (18 possibilities) Position 4: all natural aa except of K, and C (18 possibilities) Position 5: all natural aa except of K, and C (18 possibilities) Position 6: all natural aa except of K, C, and P (17 possibilities).

[0060] Peptide library 3 was constructed according to the method described above (under 2.1) for library 1.

[0061] The 6mer peptides DIDYRR, DLDYRR, and DVDYRR are examples for mimotopes that can be detected by the monoclonal antibody produced according to 1 above (D in position 1 and R in position 5 are identical with the original epitope).

[0062] 2.4. Library 4: This peptide library 4 consists of 5.times.18=90 peptides, is commercially available from Mimotopes Ltd. (Paris, France; see manufacturer's guidelines) and is designed according to the natural N-terminal A.beta.42 sequence DAEFRH.

Position 1: D (fixed) Position 2: all natural amino acids except of K and C (18 different peptides) Position 3: all natural amino acids except of K and C (18 different peptides) Position 4: all natural amino acids except of K and C (18 different peptides) Position 5: all natural amino acids except of K and C (18 different peptides) Position 6: all natural amino acids except of K and C (18 different peptides).

[0063] The individualised peptide members of library 4 are depicted in FIG. 1. Peptides no. 1, 24, 48, 56 and 80 have the original sequence of the A.beta.42 N-terminal sequence. All other peptides are candidate peptides which are tested with respect to their binding capacity to a DAEFRH-binding antibody.

2.5. ELISA with Peptide Libraries:

[0064] As mentioned above, peptide libraries 1, 2, and 3 are generated with an Applied Biosystems 431A peptide synthesizer following classical Fmoc-chemistry. The commercially available peptide library 4 is generated according to the manufacturer's description (see above and under www.mimotopes.com). The 90 peptides are C-terminally linked to a pin.

[0065] The ELISA with each of the peptide libraries have been carried out following standard protocols:

The peptide library is dissolved in 100% DMSO (final concentration 10 mg/ml). The peptide solution is further diluted in PBS. The peptide mixture is coated overnight (4.degree. C.) onto ELISA plates (Nunc Maxisorp, Germany), starting with 500 .mu.g/well, and titrated to 100 ng/well. The plates are washed 3.times. times with PBS/Tween 20 (0.1% v/v). The plates are blocked with PBS/BSA (2 h at room temperature). The plates are washed 3.times. times with PBS/Tween. The plates are incubated with biotinylated DAEFRH-specific mAb (10 .mu.g/ml in PBS) for 4 h at room temperature. The plates are washed 3.times. times with PBS/Tween. The plates are incubated with streptavidin-horseradish-peroxidase (30 min at room temperature). The plates are washed 5.times. times with PBS/Tween. The plates are incubated with ABTS+H.sub.2O.sub.2 (0.1% w/v; 10 to 45 min) and the reaction is stopped with citric acid followed by photometric evaluation (wavelength 405 nm).

3. Verification of Mimotopes by Inhibition Assay

3.1. Additional Library

[0066] In addition to the 4 libraries described above (see 2.1, 2.2, 2.3, and 2.4) a fifth library is used to define mimotope sequences. This 6mer library is commercially available at EMC microcollections (Tubingen Germany) and contains 114 different hexapeptide mixtures, one position per mixture is defined by one of all natural aa except of C (19 possibilities), the remaining 5 positions are variable:

[0067] Mixtures 01 to 06 (one position fixed, alanine A, remaining 5 variable, X):

Mixture 01: AXXXXX

Mixture 02: XXXXRX

Mixture 03: XXXXRX

Mixture 04: XXXXRX

Mixture 05: XXXXAX

Mixture 06: XXXXXA

[0068] Mixtures 07 to 12 (one position fixed, arginine R, remaining 5 variable, X):

Mixture 07: RXXXXX

Mixture 08: XXXXRX

Mixture 09: XXXXRX

Mixture 10: XXXRXX

Mixture 11: XXXXRX

Mixture 12: XXXXXR

[0069] Accordingly, mixtures 13 to 114 are designed using all natural aa except of C.

3.2. Inhibition Assay

[0070] FIGS. 2 and 3 describe the results of inhibition assays performed with mimotope peptides included in and obtained from the 5 libraries (as described). The mimotope peptides compete with the original epitope for recognition by the monoclonal antibody. Original epitope and mimotope peptides contain an additional C at the C-terminus for coupling to a protein carrier (if desired).

[0071] The following peptides are used:

TABLE-US-00001 Peptide 1737 DAEFRH Peptide 3001 DKELRI Peptide 3002 DWELRI Peptide 3003 YREFFI Peptide 3004 YREFRI Peptide 3005 YAEFRG Peptide 3006 EAEFRG Peptide 3007 DYEFRG Peptide 3008 ELEFRG Peptide 3009 SFEFRG Peptide 3010 DISFRG Peptide 3011 DIGWRG

Procedure:

[0072] ELISA plates (Nunc Maxisorp) are coated with the original peptide epitope DAEFRH (C-terminally prolonged with C and coupled to bovine serum albumin BSA) at a concentration of 0.1 .mu.g/ml peptide-BSA (100 .mu.l/well, 12 h, 4.degree. C.). After blocking with PBS/BSA 1% (200 .mu.l/well, 12 h, 4.degree. C.), the plates are washed 3.times. times with PBS/Tween. Then, biotinylated monoclonal antibody (1:2000, 50 .mu.l/well) and peptides (50 .mu.l/well) at 50, 5, 0.5, 0.05, 0.005, and 0.0005 .mu.g/ml are added for 20 min. at 37.degree. C. The plates are washed 3.times. times with PBS/Tween and are incubated with horseradish peroxidase (HRP)-labeled streptavidin (100 .mu.l/well, 30 min, RT). The plates are washed 5.times. times with PBS/Tween and are incubated with ABTS+H.sub.2O.sub.2 (0.1% w/v, 10 to 45 min) and the reaction is stopped with citric acid followed by photometric evaluation (wavelength 405 nm).

[0073] As expected and seen in FIG. 2, peptide 1737 DAEFRH can compete with BSA-coupled, plate-bound peptide DAEFRH and thus inhibits recognition by the monoclonal antibody. Furthermore, it is shown that peptide 3003 is not able to inhibit binding of the monoclonal antibody to the original epitope. In contrast, peptides 3001, 3002, 3004, 3005, 3006, and 3007 (to a different extent) block epitope recognition. Whereas peptide 3004 is only inhibitory at a high concentration (50 .mu.g/ml), peptides 3001, 3006, and 3007 are strongly inhibitory with an IC.sub.50 of less than 0.5 .mu.g/ml. Peptides 3002 and 3005 are "intermediate" inhibitors with an IC.sub.50 of more than 0.5 .mu.g/ml.

[0074] As expected and seen in FIG. 3, peptide 1737 DAEFRH can success-fully compete with BSA-coupled, plate-bound peptide DAEFRH for monoclonal antibody recognition in an additionally performed, independent experiment. Furthermore, it is shown that peptides 3010 and 3011 are not inhibitory at the concentrations tested, whereas peptides 3008 and 3009 are (relatively) weak inhibitors with an IC.sub.50 of less than 5 .mu.g/ml.

[0075] Table 1 briefly summarizes the inhibitory capacity of mimotopes included in and obtained from libraries (as described):

TABLE-US-00002 TABLE 1 Inhibitory capacity of mimotopes: Peptide 3001 DKELRI strong Peptide 3002 DKELRI intermediate Peptide 3003 YREFFI none Peptide 3004 YREFRI weak Peptide 3005 YAEFRG intermediate Peptide 3006 EAEFRG strong Peptide 3007 DYEFRG strong Peptide 3008 ELEFRG weak Peptide 3009 SFEFRG weak Peptide 3010 DISFRG none Peptide 3011 DIGWRG none

4. Inhibition Assay for Additional Mimotopes Screenend According to the Present Invention

Inhibition Assay

[0076] FIGS. 4 and 5 describe the results of inhibition assays performed with mimotope peptides included in and obtained from the 5 libraries (as described). The mimotope peptides compete with the original epitope for recognition by the monoclonal antibody. Original epitope and mimotope peptides contain an additional C at the C-terminus (position 7) for coupling to a protein carrier (if desired).

[0077] The following peptides are used:

TABLE-US-00003 Peptide 1737 DAEFRH (original epitope + C) Peptide 1234 KKELRI Peptide 1235 DRELRI Peptide 1236 DKELKI Peptide 1237 DRELKI Peptide 1238 DKELR Peptide 1239 EYEFRG Peptide 1241 DWEFRDA Peptide 4002 SWEFRT Peptide 4003 GREFRN Peptide 4004 WHWSWR

Procedure:

[0078] ELISA plates (Nunc Maxisorp) are coated with the original peptide epitope DAEFRH (C-terminally prolonged with C and coupled to bovine serum albumin BSA) at a concentration of 0.1 .mu.g/ml peptide-BSA (100 .mu.l/well, 12 h, 4.degree. C.). After blocking with PBS/BSA 1% (200 .mu.l/well, 12 h, 4.degree. C.), the plates are washed 3.times. times with PBS/Tween. Then, biotinylated monoclonal antibody (1:2000, 50 .mu.l/well) and peptides (50 .mu.l/well) at different concentrations are added for 20 min. at 37.degree. C. The plates are washed 3.times. times with PBS/Tween and are incubated with horseradish peroxidase (HRP)-labeled streptavidin (100 .mu.l/well, 30 min, RT). The plates are washed 5.times. times with PBS/Tween and are incubated with ABTS+H.sub.2O.sub.2 (0.1% w/v, 10 to 45 min) and the reaction is stopped with citric acid followed by photometric evaluation (wavelength 405 nm).

[0079] As expected and seen in FIG. 4, peptide 1737 DAEFRH can compete with BSA-coupled, plate-bound peptide DAEFRH and thus inhibits recognition by the monoclonal antibody. Furthermore, it is shown that peptide 4004 is not able to inhibit binding of the monoclonal antibody to the original epitope. In contrast, peptides 4002 and 4003 (to a different extent) block epitope recognition. Whereas peptide 4003 is only inhibitory at a relatively high concentration (10 .mu.g/ml), peptide 4002 is strongly inhibitory with an IC.sub.50 of less than 0.4 .mu.g/ml.

[0080] As expected and seen in FIG. 5, peptide 1737 DAEFRH can success-fully compete with BSA-coupled, plate-bound peptide DAEFRH for monoclonal antibody recognition in an additionally performed, independent experiment. Furthermore, it is shown that peptide 1234 is hardly inhibitory at the concentrations tested, whereas peptides 1235, 1236, 1237, 1238, 1239 and 1241 (to a different extent) block epitope recognition. Peptides 1235, 1238 and 1241 are strong inhibitors with an IC.sub.50 of less than 0.5 .mu.g/ml, whereas peptides 1236 and 1237 are (relatively) weak inhibitors with an IC.sub.50 of more than 5 .mu.g/ml. Peptide 1239 is an intermediate inhibitor with an IC.sub.50 of more than 0.5 .mu.g/ml.

[0081] Table 2 briefly summarizes the inhibitory capacity of mimotopes included in and obtained from libraries (as described):

TABLE-US-00004 TABLE 2 Inhibitory capacity of mimotopes: Peptide 1234 KKELRI none Peptide 1235 DRELRI strong Peptide 1236 DKELKI weak Peptide 1237 DRELRI weak Peptide 1238 DKELR strong Peptide 1239 EYEFRG intermediate Peptide 1241 DWEFRDA strong Peptide 4002 SWEFRT strong Peptide 4003 GREFRN weak Peptide 4004 WHWSWR none

[0082] The results presented in FIGS. 4 and 5 show that in addition to various 6mer peptides (as shown here and before), 5mer peptides (namely peptide 1238 DKELR) and 7mer peptides (namely peptide 1241 DWEFRDA) may be used as epitopes in a mimotope-based Alzheimer vaccine.

Sequence CWU 1

1

12316PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 1Asp Ala Glu Phe Arg His1 526PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 2Asp Arg Glu Phe Arg His1 536PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 3Asp Asn Glu Phe Arg His1 546PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 4Asp Asp Glu Phe Arg His1 556PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 5Asp Gln Glu Phe Arg His1 566PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 6Asp Glu Glu Phe Arg His1 576PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 7Asp Gly Glu Phe Arg His1 586PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 8Asp His Glu Phe Arg His1 596PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 9Asp Ile Glu Phe Arg His1 5106PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 10Asp Leu Glu Phe Arg His1 5116PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 11Asp Met Glu Phe Arg His1 5126PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 12Asp Phe Glu Phe Arg His1 5136PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 13Asp Pro Glu Phe Arg His1 5146PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 14Asp Ser Glu Phe Arg His1 5156PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 15Asp Thr Glu Phe Arg His1 5166PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 16Asp Trp Glu Phe Arg His1 5176PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 17Asp Tyr Glu Phe Arg His1 5186PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 18Asp Val Glu Phe Arg His1 5196PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 19Asp Ala Ala Phe Arg His1 5206PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 20Asp Ala Arg Phe Arg His1 5216PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 21Asp Ala Asn Phe Arg His1 5226PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 22Asp Ala Asp Phe Arg His1 5236PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 23Asp Ala Gln Phe Arg His1 5246PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 24Asp Ala Glu Phe Arg His1 5256PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 25Asp Ala Gly Phe Arg His1 5266PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 26Asp Ala His Phe Arg His1 5276PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 27Asp Ala Ile Phe Arg His1 5286PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 28Asp Ala Leu Phe Arg His1 5296PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 29Asp Ala Met Phe Arg His1 5306PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 30Asp Ala Phe Phe Arg His1 5316PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 31Asp Ala Pro Phe Arg His1 5326PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 32Asp Ala Ser Phe Arg His1 5336PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 33Asp Ala Thr Phe Arg His1 5346PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 34Asp Ala Trp Phe Arg His1 5356PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 35Asp Ala Tyr Phe Arg His1 5366PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 36Asp Ala Val Phe Arg His1 5376PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 37Asp Ala Glu Ala Arg His1 5386PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 38Asp Ala Glu Arg Arg His1 5396PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 39Asp Ala Glu Asn Arg His1 5406PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 40Asp Ala Glu Asp Arg His1 5416PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 41Asp Ala Glu Gln Arg His1 5426PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 42Asp Ala Glu Glu Arg His1 5436PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 43Asp Ala Glu Gly Arg His1 5446PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 44Asp Ala Glu His Arg His1 5456PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 45Asp Ala Glu Ile Arg His1 5466PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 46Asp Ala Glu Leu Arg His1 5476PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 47Asp Ala Glu Met Arg His1 5486PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 48Asp Ala Glu Phe Arg His1 5496PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 49Asp Ala Glu Pro Arg His1 5506PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 50Asp Ala Glu Ser Arg His1 5516PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 51Asp Ala Glu Thr Arg His1 5526PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 52Asp Ala Glu Trp Arg His1 5536PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 53Asp Ala Glu Tyr Arg His1 5546PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 54Asp Ala Glu Val Arg His1 5556PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 55Asp Ala Glu Phe Ala His1 5566PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 56Asp Ala Glu Phe Arg His1 5576PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 57Asp Ala Glu Phe Asn His1 5586PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 58Asp Ala Glu Phe Asp His1 5596PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 59Asp Ala Glu Phe Gln His1 5606PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 60Asp Ala Glu Phe Glu His1 5616PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 61Asp Ala Glu Phe Gly His1 5626PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 62Asp Ala Glu Phe His His1 5636PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 63Asp Ala Glu Phe Ile His1 5646PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 64Asp Ala Glu Phe Leu His1 5656PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 65Asp Ala Glu Phe Met His1 5666PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 66Asp Ala Glu Phe Phe His1 5676PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 67Asp Ala Glu Phe Pro His1 5686PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 68Asp Ala Glu Phe Ser His1 5696PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 69Asp Ala Glu Phe Thr His1 5706PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 70Asp Ala Glu Phe Trp His1 5716PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 71Asp Ala Glu Phe Tyr His1 5726PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 72Asp Ala Glu Phe Val His1 5736PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 73Asp Ala Glu Phe Arg Ala1 5746PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 74Asp Ala Glu Phe Arg Arg1 5756PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 75Asp Ala Glu Phe Arg Asn1 5766PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 76Asp Ala Glu Phe Arg Asp1 5776PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 77Asp Ala Glu Phe Arg Gln1 5786PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 78Asp Ala Glu Phe Arg Glu1 5796PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 79Asp Ala Glu Phe Arg Gly1 5806PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 80Asp Ala Glu Phe Arg His1 5816PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 81Asp Ala Glu Phe Arg Ile1 5826PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 82Asp Ala Glu Phe Arg Leu1 5836PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 83Asp Ala Glu Phe Arg Met1 5846PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 84Asp Ala Glu Phe Arg Phe1 5856PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 85Asp Ala Glu Phe Arg Pro1 5866PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 86Asp Ala Glu Phe Arg Ser1 5876PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 87Asp Ala Glu Phe Arg Thr1 5886PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 88Asp Ala Glu Phe Arg Trp1 5896PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 89Asp Ala Glu Phe Arg Tyr1 5906PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 90Asp Ala Glu Phe Arg Val1 5916PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 91Glu Ile Asp Tyr His Arg1 5926PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 92Glu Leu Asp Tyr His Arg1 5936PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 93Glu Val Asp Tyr His Arg1 5946PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 94Asp Ile Asp Tyr His Arg1 5956PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 95Asp Leu Asp Tyr His Arg1 5966PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 96Asp Val Asp Tyr His Arg1 5976PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 97Asp Ile Asp Tyr Arg Arg1 5986PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 98Asp Leu Asp Tyr Arg Arg1 5996PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 99Asp Val Asp Tyr Arg Arg1 51006PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 100Asp Lys Glu Leu Arg Ile1 51016PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 101Asp Trp Glu Leu Arg Ile1 51026PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 102Tyr Arg Glu Phe Arg Ile1 51036PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 103Tyr Ala Glu Phe Arg Gly1 51046PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 104Glu Ala Glu Phe Arg Gly1 51056PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 105Asp Tyr Glu Phe Arg Gly1 51066PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 106Glu Leu Glu Phe Arg Gly1 51076PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 107Asp Arg Glu Leu Arg Ile1 51086PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 108Asp Lys Glu Leu Lys Ile1 51096PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 109Asp Arg Glu Leu Lys Ile1 51106PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 110Gly Arg Glu Phe Arg Asn1 51116PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 111Glu Tyr Glu Phe Arg Gly1 51127PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 112Asp Trp Glu Phe Arg Asp Ala1 51136PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 113Ser Trp Glu Phe Arg Thr1 51145PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 114Asp Lys Glu Leu Arg1 51156PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 115Ser Phe Glu Phe Arg Gly1 511611PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 116Ser Glu Val Lys Met Asp Ala Glu Phe Arg His1 5 101177PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 117Met Asp Ala Glu Phe Arg His1 51188PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 118Lys Met Asp Ala Glu Phe Arg His1 51196PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 119Tyr Arg Glu Phe Phe Ile1 51206PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 120Asp Ile Ser Phe Arg Gly1 51216PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 121Asp Ile Gly Trp Arg Gly1 51226PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 122Lys Lys Glu Leu Arg Ile1 51236PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 123Trp His Trp Ser Trp Arg1 5

Claims

1-9. (canceled)

10. A method for treating Alzheimer's Disease comprising: administering to a subject in need thereof an effective amount of an isolated or purified compound comprising the following amino acid sequence: X.sub.1X.sub.2X.sub.3X.sub.4X.sub.5X.sub.6, wherein X.sub.1 is an amino acid other than C (cysteine), X.sub.2 is an amino acid other than C (cysteine), X.sub.3 is an amino acid other than C (cysteine), X.sub.4 is an amino acid other than C (cysteine), X.sub.5 is an amino acid other than C (cysteine), X.sub.6 is an amino acid other than C (cysteine), wherein said compound binds to an antibody specific for DAEFRH (SEQ ID NO: 1), but wherein X.sub.1X.sub.2X.sub.3X.sub.4X.sub.6 is not DAEFRH (SEQ ID NO: 1).

11. The method of claim 10, wherein X.sub.1 is an amino acid with a hydroxy group or a negatively charged amino acid, X.sub.2 is a hydrophobic amino acid or a positively charged amino acid, X.sub.3 is a negatively charged amino acid, X.sub.4 is an aromatic amino acid, X.sub.5 is H, K, Y, F or R, and X.sub.6 is S, T, N, Q, D, E, R, I, K, Y, or G.

12. The method of claim 10, wherein X.sub.1 is G, E, Y, S or D, X.sub.2 is I, L, V, K, W, R, Y, F or A, X.sub.3 is D or E, X.sub.4 is Y, F or L, X.sub.5 is H, F or R, and X.sub.6 is T, N, D, R, I or G.

13. The method of claim 10, wherein the compound comprises a sequence selected from the group consisting of EIDYHR (SEQ ID NO: 91), ELDYHR (SEQ ID NO: 92), EVDYHR (SEQ ID NO: 93), DIDYHR (SEQ ID NO: 94), DLDYHR (SEQ ID NO: 95), DVDYHR (SEQ ID NO: 96), DIDYRR (SEQ ID NO: 97), DLDYRR (SEQ ID NO: 98), DVDYRR (SEQ ID NO: 99), DKELRI (SEQ ID NO: 100), DWELRI (SEQ ID NO: 101), YREFFI (SEQ ID NO: 119), YREFRI (SEQ ID NO: 102), YAEFRG (SEQ ID NO: 103), EAEFRG (SEQ ID NO: 104), DYEFRG (SEQ ID NO: 105), ELEFRG (SEQ ID NO: 106), DRELRI (SEQ ID NO: 107), DKELKI (SEQ ID NO: 108), DRELKI (SEQ ID NO: 109), GREFRN (SEQ ID NO: 110), EYEFRG (SEQ ID NO: 111), DWEFRDA (SEQ ID NO: 112), SWEFRT (SEQ ID NO: 113), DKELR (SEQ ID NO: 114) and SFEFRG (SEQ ID NO: 115).

14. The method of claim 13, wherein the compound comprises DWELRI (SEQ ID NO: 101).

15. The method of claim 13, wherein the compound comprises DYEFRG (SEQ ID NO: 105).

16. The method of claim 13, wherein the compound comprises ELEFRG (SEQ ID NO: 106).

17. The method of claim 13, wherein the compound comprises DKELKI (SEQ ID NO: 108).

18. The method of claim 13, wherein the compound comprises SWEFRT (SEQ ID NO: 113).

19. The method of claim 13, wherein the compound comprises DKELR (SEQ ID NO: 114).

20. The method of claim 13, wherein the compound comprises SFEFRG (SEQ ID NO: 115).

21. The method of claim 10, wherein the compound consists of 5 to 15 amino acid residues.

22. The method of claim 10, wherein the compound is covalently-coupled to a carrier.

23. The method of claim 22, wherein said carrier is a peptide linker or a polypeptide.

24. The method of claim 22, wherein said carrier is selected from the group consisting of KLH, tetanus toxoid, albumin binding protein, bovine serum albumin and dendrimer.

25. A method for isolating a compound binding to an antibody specific for the natural N-terminal A942 sequence DAEFRH (SEQ ID NO: 1) comprising: providing a peptide compound library comprising peptides containing the following amino acid sequence X.sub.1X.sub.2X.sub.3X.sub.4X.sub.5X.sub.6, wherein X.sub.1 is an amino acid other than C (cysteine), X.sub.2 is an amino acid other than C (cysteine), X.sub.3 is an amino acid other than C (cysteine), X.sub.4 is an amino acid other than C (cysteine), X.sub.5 is an amino acid other than C (cysteine), X.sub.6 is an amino acid other than C (cysteine), wherein X.sub.1X.sub.2X.sub.3X.sub.4X.sub.6 is not DAEFRH (SEQ ID NO: 1); contacting said peptide library with an antibody which binds to DAEFRH (SEQ ID NO: 1); and isolating those members of the peptide library which bind to said antibody.

26. The method of claim 25, wherein said peptides are provided in individualized form in said library or are immobilized separately on a solid surface.

27. The method of claim 25, wherein said antibody comprises a marker which allows its detection or isolation when bound to a peptide in the library.