Doping Control Center, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea; Interdisciplinary Program of Bioengineering, Seoul National University, Seoul, 08826, Republic of Korea.
Department of Biological and Environmental Science, Dongguk University, Goyang-si, Gyeonggi-do, 10326, Republic of Korea.
Anal Chim Acta. 2024 Aug 15;1317:342887. doi: 10.1016/j.aca.2024.342887. Epub 2024 Jun 18.
Procollagen type III N-terminal peptide (P-III-NP) is a fibrosis biomarker associated with liver and cardiac fibrosis. Despite the value of P-III-NP as a biomarker, its analysis currently relies on enzyme-linked immunosorbent assays (ELISA) and radioimmunoassays (RIA), which require more than 3 h. To facilitate early diagnosis and treatment through rapid biomarker testing, we developed a one-step immunoassay for P-III-NP using a quenchbody, which is a fluorescence-labeled immunosensor for immediate signal generation.
To create quenchbodies, the total mRNA of P-III-NP antibodies was extracted from early-developed hybridoma cells, and genes of variable regions were obtained through cDNA synthesis, inverse PCR, and sequencing. A single-chain variable fragment (scFv) with an N-terminal Cys-tag was expressed in E. coli Shuffle T7, resulting in a final yield of 9.8 mg L. The fluorescent dye was labeled on the Cys-tag of the anti-P-III-NP scFv using maleimide-thiol click chemistry, and the spacer arm lengths between the maleimide-fluorescent dyes were compared. Consequently, a TAMRA-C-labeled quenchbody exhibited antigen-dependent fluorescence signals and demonstrated its ability to detect P-III-NP at concentrations as low as 0.46 ng mL for buffer samples, 1.0 ng mL for 2 % human serum samples.
This one-step P-III-NP detection method provides both qualitative and quantitative outcomes within a concise 5-min timeframe. Furthermore, its application can be expanded using a 96-well platform and human serum, making it a high-throughput and sensitive method for testing fibrotic biomarkers.
III 型前胶原氨基端肽(P-III-NP)是一种与肝纤维化和心肌纤维化相关的纤维化生物标志物。尽管 P-III-NP 作为生物标志物具有价值,但目前其分析依赖于酶联免疫吸附测定(ELISA)和放射免疫分析(RIA),这需要超过 3 小时。为了通过快速生物标志物检测促进早期诊断和治疗,我们使用淬灭体开发了一种用于 P-III-NP 的一步免疫测定法,淬灭体是一种荧光标记的免疫传感器,可立即产生信号。
为了创建淬灭体,从早期开发的杂交瘤细胞中提取了 P-III-NP 抗体的总 mRNA,并通过 cDNA 合成、反向 PCR 和测序获得了可变区基因。在 E. coli Shuffle T7 中表达具有 N 端 Cys 标签的单链可变片段(scFv),最终产量为 9.8 mg/L。使用马来酰亚胺-硫醇点击化学将荧光染料标记在抗 P-III-NP scFv 的 Cys 标签上,并比较了马来酰亚胺-荧光染料之间的间隔臂长度。结果,TAMRA-C 标记的淬灭体表现出抗原依赖性荧光信号,并证明其能够检测缓冲液样品中低至 0.46ng/mL 的 P-III-NP 和 2%人血清样品中 1.0ng/mL 的 P-III-NP。
这种一步法 P-III-NP 检测方法在短短 5 分钟内提供定性和定量结果。此外,通过使用 96 孔平台和人血清,其应用可以扩展,使其成为一种用于测试纤维化生物标志物的高通量和敏感方法。