Serodiagnosis of multiple cancers using an extracellular protein kinase A autoantibody-based lateral flow platform

化学 免疫分析 细胞外 检出限 抗体 色谱法 分子生物学 生物化学 医学 生物 免疫学
作者
Anam Rana Gul,Jyotiranjan Bal,Ping Xu,Subhadeep Ghosh,Ting Yun,Suresh Kumar Kailasa,Yeong Hyeock Kim,Tae Jung Park
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:246: 115902-115902 被引量:2
标识
DOI:10.1016/j.bios.2023.115902
摘要

Extracellular protein kinase A autoantibody (ECPKA-AutoAb) has been suggested as a universal cancer biomarker due to its higher amounts in serum of several types of cancer patients than that of normal individuals. Herein, we first developed a lateral flow immunoassay (LFIA) tool, using a sandwich format, toward ECPKA-AutoAb in human serum. For this format, 3G2 as a capture antibody was identified using hybridoma technique and a series of screenings where it showed superior capacity to recognize Enzo PKA catalytic subunit alpha (Cα), compared to other PKA antibodies and antigens. Using these components, we performed sandwich ELISA toward a mimic and real sample of ECPKA-AutoAb. As per the results, limit of detection (LOD) was found to be 135 ng/mL and ECPKA-AutoAb levels were higher in various cancer patients than in normal individuals like previous studies. Based on these results, we applied this sandwich format into LFIA tool and found that the LOD of the fabricated LFIA tool showed about 3.8 ng/mL using spiked PKA-Ab, which is significantly improved compared to the LOD of sandwich ELISA. Also, the developed LFIA tool demonstrated a remarkable ability to detect significant differences in ECPKA-AutoAb levels between normal and cancer patients within 15 min, showing a potential for point-of-care (PoC) detection. One interesting point is that our LFIA strip contains an additional conjugation pad II, named because of its position behind the conjugation pad, in which PKA Cα is dried, enabling a sandwich format.
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