Preadsorbed Particles with Cross-Shaped DNA Scaffolds Enable Spherical Nucleic Acid to Directly Respond to Protein in Complex Matrices

核酸 化学 生物分子 DNA 生物物理学 适体 核酸定量 核糖核酸 生物化学 分子生物学 生物 基因
作者
Lijie Du,Peng Yang,Fengyi Yang,D. Wenbi Lai,Xiandeng Hou,Junbo Chen
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:97 (1): 694-702 被引量:2
标识
DOI:10.1021/acs.analchem.4c05096
摘要

Spherical nucleic acids (SNAs) usually suffer from an undesired protein corona and disrupt the function of nucleic acids (e.g., aptamer), thereby compromising recognition and response to proteins in the biological environment. To overcome the unexpected protein interference, specific proteins were initially adsorbed onto magnetic particles (MPs) as a customized protein corona "shield" with fabricated nucleic acid scaffolds, forming a preadsorbed particle-based spherical nucleic acid (pap-SNA). By comparing with AuNPs-SNA or COOH-MPs, it was found that such a protein corona "shield" of pap-SNA significantly eliminated the adsorption of nonspecific proteins or other biomolecules onto the MPs' interface, thereby enabling the SNA to directly respond to proteins in complex matrices. To further reduce the interference of protein on SNA performance, a series of nucleic acid scaffolds (Z-type, dsDNA type, circle type, T-type, and cross-shaped type) were designed by changing the rigidity and thermal stability of functional nucleic acids on the MPs. As a consequence, the pap-SNA with a cross-shaped scaffold improved the sensitivity of the pap-SNA-based detection platform in that the orderly arrangement of functional nucleic acids provides a steric hindrance to interferents. Moreover, the presence of the cross-shaped scaffold not only enables pap-SNA to exhibit a proportional response to varied protein concentrations but also enhances the detection sensitivity of pap-SNA by 160% in serum and by 190% in urine. Therefore, incorporating optimized DNA scaffolds maintained and facilitated the function of a probe (aptamer) on the surface of SNA. This approach offers a pathway for creating SNA with direct response and anti-interference capability applicable to detecting diverse biomolecules such as nucleic acids and proteins in biological matrices.
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