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Evaluation of the apolipoprotein E (apoE)-HDL-associated risk factors for coronary heart disease using duo-functional
Ching-Ying Tsai1, Deng-Ying Huang2, Ja-An Annie Ho3,4,5,6
1BioAnalytical Chemistry and Nanobiomedicine Laboratory, Department of Biochemical Science and Technology, National Taiwan University, Taipei, 10617, Taiwan.
Insights
A new electrochemical aptasensor simultaneously measures apolipoprotein E-containing high-density lipoprotein (apoE-HDL), its cholesterol (apoE-HDL-C), and total HDL-C. This offers a convenient, purification-free strategy for detecting coronary heart disease biomarkers.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Cardiovascular Disease Biomarkers
Background:
- Apolipoprotein E-containing high-density lipoprotein (apoE-HDL) and its cholesterol (apoE-HDL-C) are emerging biomarkers for coronary heart disease (CHD).
- Accurate and simultaneous detection of these biomarkers is crucial for early CHD prediction.
Purpose of the Study:
- To develop a novel electrochemical aptasensor for the simultaneous determination of apoE-HDL, apoE-HDL-C, and total HDL-C.
- To establish an efficient and convenient sensing platform for CHD risk assessment.
Main Methods:
- Development of a two-stage, enzyme-assisted, dual-signal electrochemical aptasensor.
- Subsystem (I) utilizes apoE-specific aptamer and methylene blue (MB)-labeled DNA displacement for apoE-HDL detection.
- Subsystem (II) employs enzyme-based reactions and electrochemical signal amplification for quantifying apoE-HDL-C and total HDL-C.
Main Results:
- The aptasensor demonstrated a linear dynamic range of 1-100 mg/dL for apoE-HDL (R²=1.00) and 0-250 mg/dL for cholesterol standards (R²=0.98).
- Analysis of human HDL samples showed that apoE-HDL-C constituted approximately 10% of total HDL-C, aligning with prior research.
- The sensor enabled concurrent quantification without requiring sample purification.
Conclusions:
- A robust electrochemical aptasensor for simultaneous detection of key HDL-related CHD biomarkers has been successfully developed.
- This novel platform provides an efficient, convenient, and purification-free method for assessing cardiovascular risk.
- The aptasensor holds promise for advancing predictive diagnostics in coronary heart disease.
Abstract:
Apolipoprotein E containing high-density lipoprotein (apoE-HDL) and apoE-HDL cholesterol (apoE-HDL-C) are recently recognized as potential biomarkers for coronary heart disease (CHD). We herein developed a two-stage, enzyme-assisted, dual-signal aptasensor that enables a useful electrochemical sensing platform for simultaneous determination of apoE-HDL, apoE-HDL-C, and total HDL-C presented in the sample. The detection scheme consists of two subsystems. In subsystem (I), the level of apoE-HDL is evaluated upon the binding of apoE-specific aptamer and subsequently methylene blue (MB)-labeled DNA displacement occurs on the electrode surface, resulting in electrochemical reduction of methylene blue. In subsystem (II), two kinds of cholesterol levels (apoE-HDL-C and total HDL-C) can be measured. For apoE-HDL-C, the amount of cholesterol in apoE-HDL captured by the aptamer in the first step can be further determined with the aid of surfactant, cholesterol esterase, cholesterol oxidase, and p-aminophenol-mediated electrochemical signal amplification. As for total HDL-C, the amount of cholesterol is determined by the same approach as that used for apoE-HDL-C determination, but without washing (separation). The linear dynamic range for apoE-HDL determination is from 1 to 100 mg/dL (R2 = 1.00). For cholesterol standards, the linear dynamic range is determined to be 0-250 mg/dL (R2 = 0.98). Finally, serial dilutions of purified human HDL preparations were examined using the newly developed aptasensor; the percentage of apoE-HDL-C to HDL-C was found to be ~10%, which correlated well with previously reported values. In conclusion, we successfully developed an electrochemical aptasensor that allows concurrent quantification of apoE-HDL, apoE-HDL-C, and HDL-C on the same platform, offering an efficient, convenient, and purification-free sensing strategy for predictive CHD biomarkers.
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