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Published on: March 2, 2018
Peptides of neuron specific enolase as potential ASD biomarkers: From discovery to epitope mapping
Alexandra Ramirez-Celis1, Elizabeth Edmiston1, Joseph Schauer1
1Department of Internal Medicine, Division of Rheumatology, Allergy, and Clinical Immunology, University of California, One Shields Avenue, Davis, CA 95616, USA.
Insights
Maternal autoantibodies targeting Neuron Specific Enolase (NSE) are linked to autism spectrum disorder (ASD). Researchers identified specific NSE epitopes in mothers of children with ASD, suggesting potential biomarkers for early detection.
Area of Science:
- Neuroscience
- Immunology
- Genetics
Background:
- Autism spectrum disorder (ASD) affects approximately 1 in 59 children in the US.
- Maternal autoantibody-related (MAR) autism is associated with ~23% of ASD cases.
- Previous research identified seven MAR-specific autoantigens and their epitope peptides.
Purpose of the Study:
- To identify additional autoantigens targeted by maternal autoantibodies in ASD.
- To map unique ASD-specific epitopes using microarray technology.
- To investigate Neuron Specific Enolase (NSE) as a potential autoantigen.
Main Methods:
- Fetal Rhesus macaque brain tissue was analyzed using 2-D gel electrophoresis and MALDI-TOF MS.
- Neuron Specific Enolase (NSE) was identified as a target autoantigen.
- NSE was translated into peptides for microarray analysis using maternal plasma from mothers with ASD and typically developing (TD) children.
Main Results:
- Four statistically significant ASD-specific NSE-peptide sequences were identified (p < 0.05).
- Specific peptide sequences like DVAASEFYRDGKYDL and RLAKYNQLMRIEEEL showed significant differences between ASD and TD groups.
- A large immunodominant epitope recognized by both ASD and TD maternal antibodies was also identified.
Conclusions:
- Maternal autoantibodies against NSE are present in mothers of both ASD and TD children.
- Several ASD-specific NSE epitopes show potential as biomarkers for MAR ASD.
- Further studies will combine NSE analysis with previously identified MAR ASD autoantigens.
Abstract:
Autism spectrum disorder (ASD) is an important health issue and affects 1 in 59 children in the US. Prior studies determined that maternal autoantibody related (MAR) autism is thought to be associated with ~23% of ASD cases. We previously identified seven MAR-specific autoantigens including CRMP1, CRMP2, GDA, LDHA, LDHB, STIP1, and YBX1. We subsequently described the epitope peptide sequences recognized by maternal autoantibodies for each of the seven ASD-specific autoantigens. The aim of the current study was to expand upon our previous work and identify additional antigens recognized by the ASD-specific maternal autoantibodies, as well as to map the unique ASD-specific epitopes using microarray technology. Fetal Rhesus macaque brain tissues were separated by molecular weight and a fraction containing bands between 37 and 45 kDa was analyzed using 2-D gel electrophoresis, followed by peptide mass mapping using MALDI-TOF MS and TOF/TOF tandem MS/MS. Using this methodology, Neuron specific enolase (NSE) was identified as a target autoantigen and selected for epitope mapping. The full NSE sequence was translated into 15-mer peptides with an overlap of 14 amino acids onto microarray slides and probed with maternal plasma from mothers with an ASD child and from mothers with a Typically Developing child (TD) (ASD = 27 and TD = 21). The resulting data were analyzed by T-test. We found 16 ASD-specific NSE-peptide sequences for which four sequences were statistically significant (p < 0.05) using both the t-test and SAM t-test: DVAASEFYRDGKYDL (p = 0.047; SAM score 1.49), IEDPFDQDDWAAWSK (p = 0.049; SAM score 1.49), ERLAKYNQLMRIEEE (p = 0.045; SAM score 1.57), and RLAKYNQLMRIEEEL (p = 0.017; SAM score 1.82). We further identified 5 sequences that were recognized by both ASD and TD antibodies suggesting a large immunodominant epitope (DYPVVSIEDPFDQDDWAAW). While maternal autoantibodies against the NSE protein are present both in mothers with ASD and mothers of TD children, there are several ASD-specific epitopes that can potentially be used as MAR ASD biomarkers. Further, studies including analysis of NSE as a target protein in combination with the previously identified MAR ASD autoantigens are currently underway.
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