In vitro SELEX and application of an African swine fever virus (ASFV) p30 protein specific aptamer

被引:9
作者
Hu, Changchun [1 ]
Li, Shuo [1 ]
Zhou, Jie [1 ]
Wei, Dan [1 ]
Liu, Xueying [1 ]
Chen, Zhu [1 ]
Peng, Hongquan [4 ]
Liu, Xun [5 ]
Deng, Yan [1 ,2 ,3 ]
机构
[1] Hunan Univ Technol, Hunan Key Lab Biomed Nanomat & Devices, Zhuzhou 412007, Hunan, Peoples R China
[2] Univ South China, Inst Future Sci, Changsha, Hunan, Peoples R China
[3] Univ South China, Hengyang Med Sch, Hengyang 421001, Hunan, Peoples R China
[4] Kiang Wu Hosp, Dept Nephrol, Macau, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Nephrol, Guangzhou, Peoples R China
关键词
D O I
10.1038/s41598-024-53619-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The African swine fever virus (ASFV) has caused severe economic losses in the pig industry. To monitor ASFV spread, the p30 protein has been identified as an ideal infection marker due to its early and long-term expression during the ASFV infection period. Timely monitoring of ASFV p30 enables the detection of ASFV infection and assessment of disease progression. Aptamers are an outstanding substitute for antibodies to develop an efficient tool for ASFV p30 protein detection. In this study, a series of aptamer candidates were screened by in vitro magnetic bead-based systematic evolution of ligands by exponential enrichment (MB-SELEX). An aptamer (Atc-20) finally showed high specificity and affinity (Kd = 140 +/- 10 pM) against ASFV p30 protein after truncation and affinity assessment. Furthermore, an aptamer/antibody heterogeneous sandwich detection assay was designed based on Atc20, achieving a linear detection of ASFV p30 ranging from 8 to 125 ng/ml and a detection limit (LOD) of 0.61 ng/ml. This assay showed good analytical performances and effectively detected p30 protein in diluted serum samples, presenting promising potential for the development of ASFV biosensors.
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页数:10
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