Copper Ions Enhance Signal Intensity of Sandwich ELISA for Amorphous Aggregates of Amyloid-β42


Amyloid-β42 (Aβ42) accumulates within senileplaque, a pathological hall mark of Alzheimer’s disease (AD). Our previous reports showed that the monoclonal antibodies 37-11 and 77-3 react with conformational epitopes on the surface of the soluble aggregates of Aβ42 and that sandwich ELISA using these two monoclonal antibodies yields high reactivity to detect soluble aggregates of Aβ42. Here, the reactivity of the sandwich ELISA was shown to increase in the presence of 50 μM Cu2+. However, the addition of Cu2+ had only a small effect on the reactivity of a direct ELISA using antibody 37-11 or 77-3, suggesting that Cu2+ has a small effect on the number of epitopes on the surface of the aggregates. Atomic force microscopy images showed that larger aggregates were formed in the presence of Cu2+, as shown in the other reports. Cu2+ may gather the aggregates with distinct epitopes recognized by antibodies 37-11 and 77-3, leading to increased signal intensity of the sandwich ELISA.

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Itakura, A. , F. Kanematsu, Y. , Suzuki, R. , Kohno, H. and Yoshimune, K. (2016) Copper Ions Enhance Signal Intensity of Sandwich ELISA for Amorphous Aggregates of Amyloid-β42. Advances in Bioscience and Biotechnology, 7, 343-349. doi: 10.4236/abb.2016.79033.

1. Introduction

One of major hallmarks of Alzheimer’s disease (AD) is the formation of senile plaques, mainly consisting of amyloid beta protein (Aβ), in the brains of patients [1] [2] . Under physiological conditions, Aβ are produced by the partial digestions of amyloid precursor proteins; most Aβs consist of 40 amino acids (Aβ40), though approximately 10% are 42 amino acids in length (Aβ42) [3] . Aβ42 has higher hydrophobicity, and thus a higher tendency to aggregate compared to Aβ40; therefore, Aβ42 appears to be the more toxic variant [4] . Aβ42 forms two distinct aggregates known as fibrillar and amorphous forms. The fibrillar form has an antiparallel β-sheet structure, and is the main component of senile plaques [5] . The fibril formation is formed from the conversion of monomers to oligomers and subsequently to protofibrils and fibrils [6] . The amorphous aggregates are less structured and lack the ability to form fibrils. They are found in diffuse plaques [7] and senile plaques in the brains of AD patients [8] . Various sizes of amorphous aggregates have been reported ranging from trimers to sub-micrometer orders [9] - [11] . Large oval aggregates (LOA), which are amorphous aggregates greater than 200 nm in their minor axis, are generated by the addition of peptide Aβ16-20 [12] . Aβ16-20 includes the region essential for the fibril formation in Aβ but prevents fibril formation to produce LOAs. As previously described [13] , soluble aggregates are prepared by dissolving Aβ42 in 1,1,1,3,3,3-hexafluoro-2-propanol in the absence of Aβ16-20. The soluble aggregates include various sizes of amorphous aggregates ranging from 20 to 400 nm. Metal ions such as Cu2+ bind to Aβ affecting the formation of aggregates. Many reports show that Cu2+ binding changes the surface charge of Aβ and enhances amorphous aggregate formation by preventing fibril formation [14] - [18] . Aβ42 in cerebrospinal fluid (CSF) is a clinical biomarker for AD [19] [20] . In AD patients, the concentration of Aβ42 decreases, as it is incorporated into senile plaques, whereas the concentration of Aβ40 is unchanged. The average concentration of Aβ42 in spinal fluid is less than 200 Pm [19] . Therefore, highly sensitive detection of Aβ42 is desirable for AD diagnosis. Our previous reports identified various monoclonal antibodies with reactivity against Aβ aggregates, but with little reactivity against the fibril and monomer forms [8] [12] [13] [21] . Among them, antibody 37-11 was determined to react with LOA [12] , and antibody 77-3 could react with both LOA and soluble aggregates [13] . Sandwich ELISA using these two antibodies resulted in the highly sensitive detection of soluble aggregates. In this report, the reactivity of the sandwich ELISA was shown to increase through the addition of 50 μM Cu2+; however, the addition had only a small effect on the reactivity of each antibody. Cu2+ could gather aggregates to form large aggregates with two distinct epitopes that were specifically recognized by antibodies 77-3 and 37-11.

2. Materials and Methods

2.1. Preparation of the Soluble Aggregates

Soluble amorphous aggregates were prepared as previously described [21] . Briefly, 0.11 mM Aβ42 (Peptide Institute Inc., Osaka, Japan) was dissolved in 1,1,1,3,3,3-hexafluo- ro-2-propanol, and incubated at 4˚C for 16 h followed by 37˚C for 3 h, after which the solution was lyophilized. The steps including dissolution and lyophilization were repeated twice, and lyophilized Aβ42 was dissolved in deionized water. The concentration of Aβ42 in the solution was determined by its absorbance at 280 nm using the molar extinction coefficient of 1450 M−1cm−1 of Aβ42, which has one tyrosine residue and no tryptophan residues.

2.2. Enzyme-Linked Immunosorbent Assay (ELISA)

Direct ELISA was performed as previously described [12] . The soluble aggregates (100 μl) were used as solid-phase antigens, and were stained on 96-well plates (F96 MAXISORP NUNC-IMMUNO PLATE; Thermo Fisher Scientific Inc., Rochester, NY, USA). The monoclonal antibody 37-11 or 77-3, previously conjugated to HRP using a Peroxidase Labeling Kit-SH (Dojindo Molecular Technologies Inc., Kumamoto, Japan), was used as a primary antibody. The substrate SIGMAFAST OPD (Sigma-Aldrich, St. Louis, MO) was used for color development according to the manufacturer’s instructions. For sandwich ELISA, the antibody 77-3 was used as the primary antibody, and HRP-conjugated antibody 37-11 was used as the secondary antibody as described previously [13] .

2.3. Atomic Force Microscopy

The sizes and shapes of the aggregates were observed by atomic force microscopy (AFM, JSPM-5200, JEOL Ltd, Tokyo, Japan) as previously described [12] . The aggregates (10 μl) were dropped on fresh mica and dried by desiccation, and measured using the altering current mode at room temperature, with a frequency of approximately 190 kHz, typical of resonances with a 4.5 N/m spring constant.

3. Results and Discussion

3.1. Cu2+ Increases Signal Intensity of Soluble Aggregates during Sandwich ELISA

Metal ions are known to bind to Aβ and induce the formation of the amorphous aggregates. Metal ions were hypothesized to change the conformation of the epitopes, recognized by antibodies 37-11 and 77-3, and used for the highly sensitive detection of soluble aggregates. Various metal ions (50 μM MnCl2, FeCl2, NiCl2, CuCl2, or ZnCl2) were added to the soluble aggregates and signal intensities were observed after sandwich ELISA using the two antibodies. The addition of CuSO4 increased the signal intensity approximately 9.1-fold; however, the effect of other metal ions had little effect on signal intensities (data not shown). This result is consistent with the previous reports suggesting that binding of Cu2+ to Aβ is stronger than that of other metal ions. Thus, the increased signal intensity was considered to be caused by Cu2+ binding to Aβ The effect of different concentrations of CuSO4 on the signal intensity of soluble aggregates in the sandwich ELISA is shown in Figure 1. The signal increased in the presence of 10 μM CuSO4, and reached a maximum in the presence of CuSO4 ranging in concentration from 25 to 75 μM. These concentrations of Cu2+ were much higher than those of Aβ (130 nM in 100 μl), used for the ELISA, and may have induced the formation of amorphous aggregates. Some studies have shown that Cu2+ at sub-equimolar metal ion/Aβ42 ratios induces the formation of fibrils, whereas supra-molar ratios induce the formation of non-fibrillar forms [15] . In addition, the Cu2+ concentrations in this report were similar to those found in the serum (7 - 41 μM) [22] . Figure 2 shows the effects of CuSO4 and CuCl2 on the signal intensities of the sandwich ELISA. The effect of CuCl2 was greater than that of CuSO4 suggesting that the counter anion also affects signal intensity.

Figure 1. Effect of CuSO4 concentrations on the signal intensity of the sandwich ELISA. Sandwich ELISA was performed using the antibody 77-3 as a primary antibody and HRP-conjugated antibody 37-11 as a secondary antibody. The reactivity of the soluble aggregates (13 pmol), in the presence and absence of various concentrations of Cu2+, was determined.

Figure 2. Effect of CuSO4 and CuCl2 on the signal intensity of the sandwich ELISA. Sandwich ELISA using the antibodies 37-11 and 77-3 was performed in the absence (circles) and presence of 50 μM CuSO4 (triangles) or CuCl2 (squares).

3.2. Cu2+ Has Little Effect on the Signal Intensity of the Soluble Aggregates from Direct ELISA

It is possible that the epitopes, recognized by antibodies 37-11 and 77-3, are formed on the surface of soluble aggregates in the presence of Cu2+. To evaluate the formation of new epitopes, direct ELISA was performed. Figure 3 shows the effect of 50 μM CuCl2 on signal intensities. Unlike the results of the sandwich ELISA (Figure 2), Cu2+ only minimally enhanced the signal intensity. These results suggest that Cu2+ increases the intensity by gathering distinct aggregates with two distinct epitopes recognized by antibodies 37-11 and 77-3, rather than generating these epitopes. The AFM images (Figure 4), showing the formation of larger aggregates through the addition of Cu2+, were

(a) (b)

Figure 3.Effect of CuCl2 on the signal intensity of the direct ELISA. Direct ELISA using HRP-conjugated antibody 37-11 (a) or 77-3 (b) was performed in the absence (open squares) and the presence of 50 μM CuCl2 (closed circles).

(a) (b)

Figure 4. AFM images of soluble aggregates. Soluble aggregates in the absence (a) and presence (b) of 50 μM CuCl2 are shown.

consistent with this theory. Based on this hypothesis, the epitopes recognized by antibodies 37-11 and 77-3 might be separately located on the surface of distinct aggregates, and few aggregates have both epitopes on their surface.

This report shows that the addition of Cu2+ increases the reactivity of the sandwich ELISA for soluble aggregates. This finding could contribute to the development of a precise and highly sensitive ELISA for Aβ aggregates by enhancing the reactivity of the antibodies.

Conflicts of Interest

The authors declare no conflicts of interest.


[1] Awasthi, M., Singh, S., Pandey, V.P. and Dwivedi, U.N. (2016) Alzheimer’s Disease: An Overview of Amyloid Beta Dependent Pathogenesis and Its Therapeutic Implications along with In Silico Approaches Emphasizing the Role of Natural Products. Journal of Neurological Sciences, 361, 256-271.
[2] Hardy, J.A. and Higgins, G.A. (1992) Alzheimer’s Disease: The Amyloid Cascade Hypothesis. Science, 256, 184-185.
[3] vanOijen, M., Hofman, A., Soares, H.D., Koudstaal, P.J. and Breteler, M.M. (2006) Plasma Abeta(1-40) and Abeta(1-42) and the Risk of Dementia: A Prospective Case-Cohort Study. Lancet Neurology, 5, 655-660.
[4] Suzuki, N., Cheung, T.T., Cai, X.D., Odaka. A., Otvos, L. Jr., Eckman, C., Golde, T.E. and Younkin, S.G. (1994) An Increased Percentage of Long Amyloid Beta Protein Secreted by Familial Amyloid Beta Protein Precursor (Beta APP717) Mutants. Science, 264, 1336-1340.
[5] Chimon, S., Shaibat, M.A., Jones, C.R., Calero, D.C., Aizezi, B. and Ishii, Y. (2007) Evidence of Fibril-Like β-Sheet Structures in a Neurotoxic Amyloid Intermediate of Alzheimer’s β-Amyloid. Nature Structural & Molecular Biology, 14, 1157-1164.
[6] O'Nuallain, B., Freir, D.B., Nicoll, A.J., Risse, E., Ferguson, N., Herron, C.E., Collinge, J. and Walsh, D.M. (2010) Amyloid Beta-Protein Dimers Rapidly Form Stable Synaptotoxicprotofibrils. The Journal of Neuroscience, 30, 14411-14419.
[7] Dickson, D.W. (1997) The Pathogenesis of Senile Plaques. Journal of Neuropathology & Experimental Neurology, 56, 1285-1290.
[8] Ochiishi, T., Itakura, A., Liu, L., Akatsu, H., Kohno, H., Nishimura, M. and Yoshimune, K. (2016) Immunohistochemical Detection of the Delayed Formation of Nonfibrillar Large Amyloid-β Aggregates. Genes Cells, 21, 200-211.
[9] Lambert, M.P., Barlow, A.K., Chromy, B.A., Edwards, C., Freed, R., Liosatos, M., Morgan, T.E., Rozovsky, I., Trommer, B., Viola, K.L. and other 5 authors (1998) Diffusible, Nonfibrillar Ligands Derived from Abeta1-42 Are Potent Central Nervous System Neurotoxins. The Proceedings of the National Academy of Sciences of the United States of America, 95, 6448-6453.
[10] Barghorn, S., Nimmrich, V., Striebinger A., Krantz, C., Keller, P., Janson, B., Bahr, M., Schmidt, M., Bitner, R.S., Harlan, J., et al. (2005) Globular Amyloid Beta-Peptide Oligomer —A Homogenous and Stable Neuropathological Protein in Alzheimer’s Disease. Journal of Neurochemistry, 95, 834-847.
[11] Matsumura, S., Shinoda, K., Yamada, M., Yokojima, S., Inoue, M., Ohnishi, T., Shimada, T., Kikuchi, K., Masui, D., Hashimoto, S. and other 14 authors (2011) Two Distinct Amyloid Beta-Protein (Abeta) Assembly Pathways Leading to Oligomers and Fibrils Identified by Combined Fluorescence Correlation Spectroscopy, Morphology, and Toxicity Analyses. Journal of Biological Chemistry, 286, 11555-11562.
[12] Shimizu, T., Yoshimune, K., Komoriya, T., Akiyama, T., Ye, X. and Kohno, H. (2013) Monoclonal Antibodies against Large Oval Aggregates of Aβ1-42. Journal of Bioscience and Bioengineering 115, 216-220.
[13] Shimizu, T., Yoshimune, K., Komoriya, T., Akiyama, T., Ye, X. and Kohno, H. (2013) Combination of Specific Monoclonal Antibodies Allow Identification of Soluble Aggregates of Aβ1-42 by Sandwich ELISA. Advances in Bioscience and Biotechnology, 4, 63-66.
[14] Branch, T., Girvan, P., Barahona, M. and Ying, L. (2015) Introduction of a Fluorescent Probe to Amyloid-β to Reveal Kinetic Insights into Its Interactions with Copper(II). Angewandte Chemie International Edition, 54, 1227-1230.
[15] Ryan, T.M., Kirby, N., Mertens, H.D., Roberts, B., Barnham, K.J., Cappai, R., Pham, Cle L., Masters, C.L. and Curtain, C.C. (2015) Small Angle X-Ray Scattering Analysis of Cu(2+)-Induced Oligomers of the Alzheimer’s Amyloid β Peptide. Metallomics, 7, 536-543.
[16] Jiang, D., Rauda, I., Han, S., Chen, S. and Zhou, F. (2012) Aggregation Pathways of the Amyloid β(1-42) Peptide Depend on Its Colloidal Stability and Ordered β-Sheet Stacking. Langmuir, 28, 12711-12721.
[17] Shimanouchi, T., Onishi, R., Kitaura, N., Umakoshi, H. and Kuboi, R. (2011) Copper-Mediated Growth of Amyloid β Fibrils in the Presence of Oxidized and Negatively Charged Liposomes. Journal of Bioscience and Bioengineering, 112, 611-615.
[18] Tougu, V., Karafin, A., Zovo, K., Chung, R.S., Howells, C., West, A.K. and Palumaa, P. (2009) Zn(II)- and Cu(II)-Induced Non-Fibrillar Aggregates of Amyloid-Beta (1-42) Peptide Are Transformed to Amyloid Fibrils, Both Spontaneously and Under the Influence of Metal Chelators. Journal of Neurochemistry, 110, 1784-1795.
[19] Blennow, K., Mattsson, N., Scholl, M., Hansson, O. and Zetterberg, H. (2015) Amyloid Biomarkers in Alzheimer’s Disease. Trends in Pharmacological Sciences, 36, 297-309.
[20] Holtta, M., Hansson, O., Andreasson, U., Hertze, J., Minthon, L., Nagga, K., Andreasen, N., Zetterberg, H. and Blennow, K. (2013) Evaluating Amyloid-β Oligomers in Cerebrospinal Fluid as a Biomarker for Alzheimer’s Disease. PLoS One, 8, e66381.
[21] Shimizu, T., Yoshimune, K., Komoriya, T., Ogawa, M., Akiyama, T., Ye, X. and Kohno, H. (2015) Classification of Monoclonal Antibodies to Measure the Progress of Aβ1-42 Aggregation. Global Journal for Research Analysis, 4, 117-119.
[22] Twomey, P.J., Viljoen, A., House, I.M., Reynolds, T.M. and Wierzbicki, A.S. (2005) Relationship between Serum Copper, Ceruloplasmin, and Non-Ceruloplasmin-Bound Copper in Routine Clinical Practice. Clinical Chemistry, 51, 1558-1559.

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