Abstract

Background S-Adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) are relevant to a variety of diseases. Previous reports that quantified SAM and SAH were based on HPLC or LC–MS/MS. No antibody against SAM has been generated, and the antibody against SAH cannot be used with blood samples. Immunoassays have not been used to measure SAM and SAH. In this study, ELISA was used to measure blood SAM and SAH levels.ResultsSpecific antibodies against SAM were produced for the first time using a stable analog as the antigen. The monoclonal antibodies against SAM and SAH were characterized. No cross-reactivity was detected for the analyzed analogs. For the anti-SAM antibodies, the ELISA sensitivity was ~2 nM, and the affinity was 7.29 × 1010 L/mol. For the anti-SAH antibodies, the sensitivity was ~15 nM, and the affinity was 2.79 × 108 L/mol. Using high-quality antibodies against SAM and SAH, immunoassays for the detection of SAM and SAH levels in blood and tissue samples were developed. Clinical investigations using immunoassays to measure SAM, SAH and the methylation index (MI) in normal and diseased samples indicated that (1) the SAM level is age and gender dependent; (2) the SAM level is associated with the severity of liver diseases, inflammatory reactions and other diseases; and (3) the methylation index (MI) is significantly reduced in many diseases and may serve as a screening biomarker to identify potentially unfavorable health conditions.ConclusionIt is possible to generate antibodies against active small biomolecules with weak immunogenicity, such as SAM and SAH, using traditional hybridoma technology. The antigens and antibodies described here will contribute to the development of immunoassays to measure SAM, SAH and related molecules. These assays enable the MI to be measured specifically, accurately, easily and quickly without costly equipment. This preliminary study indicates that the MI could be an effective indicator of general health, except under conditions that may alter the value of the MI, such as special diets and medications.Electronic supplementary materialThe online version of this article (doi:10.1186/s13104-016-2296-8) contains supplementary material, which is available to authorized users.

Highlights

  • S-Adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) are relevant to a variety of diseases

  • The best way to demonstrate that the newly developed anti-SAM antibody binds to SAM is to confirm that the anti-SAM antibody can bind to in vitro-synthesized SAM identical to the SAM synthesized in living cells

  • Dosage-dependent competition was detected as the sample was added to the Competitive ELISA (cELISA) system; SAM from the sample competed with the coated SAM hapten to bind the HRP-conjugated antibody 118-6

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Summary

Introduction

S-Adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) are relevant to a variety of diseases. Combined administration of N-acetyl cysteine (an antioxidant and glutathione precursor that protects against Abeta neurotoxicity), acetyll-carnitine (increases ATP levels, protects mitochondria, and buffers Abeta neurotoxicity), and S-adenosylmethionine (facilitates glutathione usage and maintains acetylcholine levels) enhances or maintains cognitive function and attenuates or prevents aggression, in mouse models of aging and neurodegeneration. Treatment with this nutraceutical combination can compensate for a lack of dietary folate and vitamin E [2]. Hydrolysis of SAH yields HCys, which is converted to cystathionine, cysteine, and glutathione, the hepatocellular antioxidant and life-saving detoxification agent Aminopropylation is another process that is initiated by SAM through decarboxylation. Methylthioadenosine (MTA), the by-product of polyamine synthesis, is a powerful analgesic and anti-inflammatory agent that may be responsible for the clinical benefits observed in the treatment of osteoarthritis, rheumatoid arthritis and fibromyalgia with SAM [3, 4]

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