BioMed Research International
Volume 2015 (2015), Article ID 267989, 8 pages
http://dx.doi.org/10.1155/2015/267989

Research Article

Epitope Fingerprinting for Recognition of the Polyclonal Serum Autoantibodies of Alzheimer’s Disease

Luiz Carlos de Oliveira-Júnior,1,2 Fabiana de Almeida Araújo Santos,³ Luiz Ricardo Goulart,³ and Carlos Ueira-Vieira¹

¹Laboratório de Genética, Instituto de Genética e Bioquímica, Universidade Federal de Uberlândia, Rua Acre s/n, Bloco 2E sala 230, Campus Umuarama, 38400-902 Uberlândia, MG, Brazil
²Faculdade de Medicina, Universidade Federal de Uberlândia, Avenida Para 1720, Bloco 2U sala 23, Campus Umuarama, 38400-902 Uberlândia, MG, Brazil
³Laboratório de Nanobiotecnologia, Instituto de Genética e Bioquímica, Universidade Federal de Uberlândia, Rua Acre s/n, Bloco 2E sala 230, Campus Umuarama, 38400-902 Uberlândia, MG, Brazil

Received 28 June 2014; Accepted 18 February 2015

Academic Editor: Giovanni Scapagnini

Copyright © 2015 Luiz Carlos de Oliveira-Júnior et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Autoantibodies (aAb) associated with Alzheimer’s disease (AD) have not been sufficiently characterized and their exact involvement is undefined. The use of information technology and computerized analysis with phage display technology was used, in the present research, to map the epitope of putative self-antigens in AD patients. A 12-mer random peptide library, displayed on M13 phages, was screened using IgG from AD patients with two repetitions. Seventy-one peptides were isolated; however, only 10 were positive using the Elisa assay technique (Elisa Index > 1). The results showed that the epitope regions of the immunoreactive peptides, identified by phage display analysis, were on the exposed surfaces of the proteins. The putative antigens MAST1, Enah, MAO-A, X11/MINT1, HGF, SNX14, ARHGAP 11A, APC, and CENTG3, which have been associated with AD or have functions in neural tissue, may indicate possible therapeutic targets.

1. Introduction

Alzheimer’s disease (AD) is the most important cause of dementia. Its prevalence increases with age and, together with increasing life expectancy, has created the expectation of an increase in the number of cases, especially in developed countries [1–4]. Due to its devastating effect on cognition and high social and economic cost [5, 6], AD has become an important subject of research and, due to its characteristics, is also a challenge. This is especially true since the neurodegenerative process may progress for many years before clear behavioral and cognitive symptoms permit diagnosis [7, 8].

Following the original description of AD in 1906, the presence of β-amyloid (Aβ) deposits, senile plaques (SP), and neurofibrillary tangles (NFT) has been established as key markers of the disease [9, 10]. The search for improved understanding of its development has focused on these components, which have also been linked to numerous other neurobiological processes as well as genetic and environmental factors [11]. Despite extensive research, our understanding of AD is still limited because accurate diagnosis of the onset of the disease is often not possible [12].

Soon after it was observed that SP and NFT are accompanied by an inflammatory process in the immune system, this system began to be investigated regarding its role in AD pathogenesis [13, 14]. As in other central nervous system diseases, Parkinson’s disease, Lewy corpuscles dementia, and obsessive compulsive disorder, there appears to be a relationship between inflammatory processes and humoral response to AD [15, 16].

Several studies have discovered an abundant presence of antibodies directed at targets in brain neural tissue, cerebrospinal fluid, and the serum of patients with AD. Antibodies against neurotransmitter receptors (glutamate, dopamine, serotonin, and acetylcholine), enzymes (ATP synthase and aldolase), cytoskeletal proteins, and microglia have been described [17–20]. Their role in the development of Alzheimer’s disease is still uncertain and may simply be the result of neuronal death from exposure to autoantigens or may have some contribution to the pathological process [21–23]. The characterization of these autoantibodies (aAb), their antigens, and their role in disease may be a means for the development of improved diagnostic tools and the identification of new therapeutic targets.

Phage display (Ph.D.) technology is useful for the identification of peptides or antibodies on the surface of the filamentous M13 bacteriophage capsid. This capsule permits exposure to an extensive diversity of peptides that can bind to various targets and be identified using peptide library techniques. This methodology has been proven useful not only for the selection of peptides that mimic proteins but also for the identification and description of epitopes recognized by antibodies [24, 25]. It also allows for the production of the monoclonal antibodies used to treat several diseases, vaccines, and diagnostic tests as well as several uses in nanotechnology [26].

Phage display findings can be analyzed with different bioinformatic tools: the identification of consensus motifs among selected sequences, the identification of possible targets by linear and conformational (3D structure) comparison with protein databanks, and assessments of their putative epitopes with their degree of antigenicity. This information can be extremely useful for planning experiments, designing drugs, and other applications [27–29].

The present study identified mimetic peptides of target antigens in the circulating IgG present in the serum of patients with AD. Our use of the phage display technique, together with bioinformatic tools, may represent one of the first evidences of the presence of autoantibodies and their putative epitope mapping, in AD.

2. Materials and Methods

2.1. Recruitment of Patients, Diagnostic Criteria, and Sample Collection

Serum samples from AD patients and healthy controls, matched by sex and age, were obtained from the University Hospital of Uberlandia. For the diagnosis of dementia, the DSM-IV TR criteria were used [30] and for the diagnosis of AD we used the criteria of the National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer’s Disease and Related Disorders Association (NINCDS-ADRDA) [31]. Patients were stratified according to the Clinical Dementia Rating (CDR), Portuguese version [32]. The controls were evaluated using the Mini-Mental State Exam [33]. This research was approved by the Research Ethics Committee of the Federal University of Uberlandia (number 304/09).

2.2. Selection of Peptides That Mimic AD Self-Antigens (Mimotopes)

The phage selection was performed using a pool of sera from AD patients and healthy (control) individuals. Immunoglobulin G (IgG) was secured using magnetic beads coupled to protein G Dynabeads (Invitrogen). For subtraction of nonspecific peptides, 10 μL of the M13 phage library (PhD12, New England Biolabs Inc.; 1 × 10¹¹ viral particles) was added to 190 μL of TBS-Tween 0.1%. After 30 minutes of incubation, magnetic separation was performed. The phage eluate was subtracted two more times prior to the positive selection, which was performed for 30 minutes against IgG-coupled beads of AD patients, completing one selection cycle. This procedure was repeated twice. Finally, bound phages were recovered from the beads by acid elution (500 μL of glycine, pH 2) for 10 minutes and then neutralized with 75 μL of Tris (pH 9).

Selected phages were amplified, purified, and titrated according to the Ph.D. Phage Display Libraries Instruction Manual (New England Biolabs).

2.3. DNA Extraction and Sequencing

After three rounds of selection, 96 blue colonies were randomly selected and their phage single strand DNA was isolated using iodide buffer extraction procedures [34].

2.4. Bead-ELISA (Enzyme Linked Immunosorbent Assay in Bead)

The selected peptide-phage clones were used in the bead-ELISA assay against IgG from controls and AD patients to evaluate their reactivity and specificity.

Fifty microliters of phage supernatant was incubated with IgG coupled in magnetic beads (Invitrogen) for one hour with stirring, at room temperature. Using a magnetic apparatus, the microspheres were precipitated, washed six times with TBS-T 0.1%, and incubated with monoclonal anti-M13 peroxidase conjugate (GE Healthcare) diluted 1 : 5000 in TBS-T 0.1% and 5% BSA for one hour with stirring, at room temperature. Microspheres were again precipitated and washed six times and the reaction was observed with buffer orthophenylenediamine (OPD) to 1 mg/mL plus 3% hydrogen peroxide (H₂O₂). The results were expressed as an arbitrary ELISA Index (EI) and calculated as follows: EI = Abs of serum sample/cut-off, where the cut-off was determined as the mean absorbance of the negative control sera plus two standard deviations. Values of EI > 1.0 were considered positive.

2.5. Bioinformatics

The vector sequences were removed and the deductions of peptide sequences were performed using the ExPASy Translate Tool (http://web.expasy.org/translate). Afterwards, the peptide sequences were submitted to in silico analysis (Figure 1).

Figure 1: Bioinformatics workflow.

For a more detailed analysis, the sequence of positive peptides selected by the ELISA assay (EI > 1) was subjected to alignment using the BLAST tool (http://blast.ncbi.nlm.nih.gov/) and compared with those available in the database of nonredundant protein sequences using the BLASTP algorithm, limiting the search to Homo sapiens sequences.

The proteins indicated in alignment were selected for the next step of the analysis. We excluded unnamed sequences which had only been predicted or that were from unknown proteins. Those sequences with low -value were analyzed to determine whether the region of alignment with the peptide was a predicted epitope using BepiPred (http://www.cbs.dtu.dk/services/BepiPred/) [35] for linear B-cell epitopes and CBTOPE (http://www.imtech.res.in/raghava/cbtope/) for conformational B-cell epitopes [36]. If the region of alignment was found to be a predicted epitope and the three-dimensional structure was available in a protein databank format (http://www.rcsb.org/pdb/home/home.do), this protein was selected for the next step of analysis.

The program PEPSURF (http://pepitope.tau.ac.il/) was used to map the putative mimotope selected by phage display in the three-dimensional protein structure of the protein [29].

2.6. Statistical Analysis

Statistical analysis was performed using the GraphPad Prism version 5.00 (GraphPad Software Inc.).

3. Results

In this study 100 patients who had registered cognitive disorders were evaluated. Only 10 of these patients had complete AD diagnosis with laboratory tests, imaging, and assessment of cognitive function by neuropsychological tests. As paired healthy control (HC), we used 10 cognitively healthy individuals.

Phage display selection of a 12-mer random peptide library generated 75 peptides, of which 71 were distinct sequences. A phage ELISA assay was performed with these clones using a pool of serum from the patients and from the controls. The result showed that of the 71 peptides, only 10 were highly reactive mimotopes when compared with the controls (IE > 1). This suggested that circulating IgG from AD patients recognizes these specific peptides (Figure 2).

Figure 2: Detection of IgG antimimotope in serum from patients with Alzheimer’s disease by Elisa using peptide-phage selected by phage display. Values of EI > 1.0 were considered positive (Student’s t-test, ). For clarity, peptides with Elisa Index values lower than 1 were omitted.

Those peptides with distinct sequences were subsequently chosen for in-depth characterization through bioinformatics. The data are presented in Table 1. As can be seen, only nine sequences of peptides led to the identification of targets according to established criteria for the bioinformatics analysis.

Table 1: Peptide sequence and position of alignment in putative Alzheimer’s disease self-antigens.

Clone
Peptide sequence
Alignment region
Putative protein matched
PDB
Accession number
NCBI

ALZ01
TSISINPPRRPS
672–683
MAST1
2M9X
AAH27985.2

ALZ02
SRPRPLIRNRRP
341–350
Enah
2XQN
AAH65238.1

ALZ03
MTIRRHRHRPKI
128–131
MAO-A
2Z5Y
P21397.1

ALZ04
SRRRIPRINRPQ
431–438
X11/MINT1
1X11
Q02410.3

ALZ05
KRRNTILINLPN
4–9
HGF
2HGF
P14210.2

ALZ06
TPIKKMIRRLPH
—
—
—
—

ALZ07
LPTKRIIKRMRR
502–508
SNX14
4BGJ
Q9Y5W7.3

ALZ08
MSLNLRMRPMRI
449–453
ARHGAP 11A
3EAP
Q6P4F7.2

ALZ09
KMTRRTHINQIS
111–115
APC
1AUT
1AUT_C

ALZ10
RSIPRIHINTTN
235–246
CENTG3
3IHW
3IHW_A

After the initial identification of targets for alignment and prediction of linear and structural epitopes, the three-dimensional alignment, using the PepSurf program, was performed. This result demonstrated that peptide sequences from phage display were mapped in exposed regions (external surfaces) of target proteins and could be accessible to antibodies (Figure 3).

(a)

(b)

(c)

(d)

(e)

(f)

(g)

(h)

(i)

Figure 3: Three dimensional epitope prediction using the PepSurf program. The peptide alignment regions are shown in red. All of the peptides align with external regions. (a) MAST1; (b) Enah; (c) MAO-A; (d) X11/MINT1; (e) HGF; (f) SNX14; (g) ARHGAP 11A; (h) APC; (i) CENTG3. Source: Martz E. FirstGlance in Jmol (http://firstglance.jmol.org).

4. Discussion

Phage display technology can be considered a subtractive proteomic strategy for the selection of specific molecules without known targets. This is due to its combinatorial nature, favoring the random binding to several molecules. It is, for this reason, an important tool for the identification of biomolecules because it exposes a large variety of ligands to many targets at the same time and requires only minimal knowledge of the starting proteome/immunome target [37]. However, this technology has a great disadvantage: only linear or simple cyclic peptides can be incorporated into phage pIII protein [38].

Since there was the possibility of the phage binding on components of the screening system such as plastic, magnetic bead, protein G [39], or irrelevant IgG, we performed a subtractive selection twice using IgG from a binding assay of healthy controls before selection with IgG from Alzheimer’s patients. This precaution was taken to avoid the selection of peptides binding in the background.

Our selection and analysis strategy resulted in the identification of ten potential mimotopes recognized by the IgG present in the serum of patients with AD. It was possible to select peptides by phage display and prevalidate them as potential new products for specific diagnosis of thyroid cancer [34], neurocysticercosis [40, 41], leishmaniasis, dengue, and leprosy [42]. The peptides selected in this work are also new potential tools for developing specific serum diagnostics for AD. Evaluation with large samples will be necessary for validation in serum platforms such as the ELISA assay.

Autoantibodies are important for AD progression. Patients with AD have a low titer of serum levels of the anti-beta-amyloid antibodies (Aβ1–42, Aβ1–15 and Aβ16–30) compared with age matched non-AD controls [43]. Antibodies against Aβ have potential use in AD treatment [44, 45]. However, the action of the autoantibodies on other neuroproteins is still unclear.

The putative epitopes of the self-antigens, using the mimotopes, were mapped and are presented in Table 2. The target proteins have an important function in the central nervous system or are involved in AD (Table 2).

Table 2: Identity of the self-antigens mapped by mimotopes.

Database ID
Description
Protein

AAH27985.2
Microtubule associated serine/threonine kinase 1
MAST1

AAH65238.1
Enabled homolog (Drosophila)
ENAH

P21397.1
Monoamine oxidase A
MAOA

Q02410.3
Amyloid beta (A4) precursor protein-binding, family A, member 1
APBA1

P14210.2
Hepatocyte growth factor (hepapoietin A; scatter factor)
HGF

Q9Y5W7.3
Sorting nexin 14
SNX14

Q6P4F7.2
Rho GTPase activating protein 11A
ARHGAP11A

NM_000312
Protein C (inactivator of coagulation factors Va and VIIIa)
PROC

AF413079.1
Homo sapiens centaurin gamma 3 mRNA
CENTG3

The ALZ01 peptide is aligned with the MAST1 sequence. MAST1 is a member of the microtubule associated serine/threonine kinase family [35]. It is an important component of the postsynaptic region [46] and one of the differentially expressed genes in the brain of patients with AD [47].

The Enah or Mena proteins, with which peptide ALZ02 is aligned, are a component of the neural growth cone [48], important for neural development [49] and axonal structure [50].

Alz03 is a putative mimotope of MAO-A, an important enzyme of the catecholamine pathway. Some studies have shown changes of the catecholamine in AD. NE levels are decreased in the hippocampus of patients with AD [51]. In addition, specific variants of PS1, an important enzyme in the formation of Ab, could influence the catalytic activity of MAO-A [52].

The ALZ04 peptide sequence is aligned with the X11 protein family. These proteins, also known as Mints or APBA (APP binding family A), are multidomain adaptor proteins [53]. They are involved in many cellular processes important for neuronal function including the regulation of ion channel function, cellular traffic, synaptic vesicle docking, and exocytosis. The X11s proteins are also involved in APP processing [54, 55]. The Mint1 PTB domain interacts with APP, regulating its traffic. Several studies have shown that gene deletion or suppression interferes with the Ab levels [56].

Another interesting mimotope of a putative self-antigen identified in the present research was the HGF. This polypeptide is a growth factor that acts like a semaphorin in the neural development [57]. Some studies have shown that levels of HGF are increased in the cerebrospinal fluid of patients with AD [58]. Also, in the brain of patients with AD, there is an increase in HGF expression which may indicate a response to injury [59].

The SNX14 protein, also mapped by the peptides from phage display, is an important element for endocytosis and endosomal signaling [60]. It has been shown, in mice, that it regulates the intrinsic excitability of pyramidal neurons [61]. The SNX12, another family member of nexins sorting, is involved in the development of the cerebral cortex [62] and regulates the endocytosis of BACE-1 [63]. Its levels are diminished in the brains of AD patients [64].

The APC protein, in mice, was found to reduce the production of Ab. The mechanism involved appears to be a stimulation of the alpha secretase activity [65]. The intracerebral infusion of APC also reduced the excitotoxicity mediated by NMDA receptors [66].

The CENTG3 antibody, also known as AGAP3 and mapped by our mimotopes, is important for AMPA receptor traffic to the neural membrane during long term potentiation, which strengthens the synapse [67]. An alternative splicing variant of AGAP3, CRAG, acts like a semaphorin [68].

The involvement of aAb in neurodegenerative diseases can be varied and uncertain. Antibodies can act as receptor agonists or antagonists, coagonists, activate the complement proteins, or lead to internalization of receptors [15]. These aAb can act directly in the disease process or may be formed only as a consequence of the exposure to new antigens by neuronal death. But, interestingly, they may also become potential biomarkers to improve understanding of AD biology and progression.

The role of aAb in AD has not been determined despite frequent descriptions of its presence in the serum and cerebrospinal fluid of AD patients. Some aAb, such as that generated against Aβ, appear to prevent the deposition and formation of fibrils and plaques by reducing neurotoxicity. Their presence in healthy individuals suggests a homeostatic role [22, 23].

Nagele et al. [69] identified several self-antigens through protein microarrays by demonstrating the presence of various aAb in the serum of patients with AD. The antigens with higher aAb reactivity were suggested as potential biomarkers. Many of the putative self-antigens identified in this study have a clear involvement with AD but the effective participation of these aAb in AD is still to be determined.

The use of mimic peptide as a diagnostic, rather than full protein, may yield increases in the specificity of the in vitro reaction. Since only the reactive region of the biomarker target will be in contact with the antibody, the background reactions tend to be low. Further studies with large sample sizes are necessary to define the potential of the mimotope peptide here isolated as a new biomarker.

5. Conclusion

The combination of in silico approaches and phage display technology was found to be an important tool in the identification of putative novel targets in Alzheimer’s disease. The success of our epitope fingerprinting was based on a strategy that involved performing a subtractive selection against the IgG of AD patients. We identified mimotopes that mimic self-antigens and these mimotopes were recognized by the autoantibodies of AD patients, which may indicate potential usefulness in the diagnosis of this disease.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This research was supported by Grants from the following Brazilian research agencies: Fundação de Amparo a Pesquisa de Minas Gerais (FAPEMIG-APQ CBB-APQ-01952-13), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, 445679/2014-0), and Coordenação de Aperfeiçoamento de Pessoal de Ensino Superior (CAPES).

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