Novel Tetrazolium-Based Colorimetric Assay for Helicase nsp13 in SARS-CoV-2

BioChem Pub Date : 2024-05-15 DOI:10.3390/biochem4020006
Triet M. Pham, Morgan G. Howard, Shane M. Carey, Lindsey R. Baker, Edward L. D’Antonio
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Abstract

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is a human pathogenic virus that encodes for a helicase (SC2Hel) that is essential for viral replication. SC2Hel has the ability to unravel dsRNA or dsDNA in an NTP-dependent manner from the 5′ to 3′ directionality. The standard helicase assay from studies involving SARS-CoV and SARS-CoV-2 have relied on the concept of fluorescence resonance energy transfer. Adding to the collection of helicase assays, herein, we have developed a novel tetrazolium-based colorimetric assay system for the detection of ADP that is produced via SC2Hel activity. This SC2Hel assay combines three enzyme-coupled steps involving the ADP-dependent Thermococcus litoralis glucokinase (TlGlcK), Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase (LmG6PDH), and Clostridium kluyveri diaphorase (CkDIA). Iodonitrotetrazolium chloride (INT), a colorimetric tetrazolium reagent, was used in the final step of the assay that converted into INT-formazan during reduction. INT-formazan in the assay’s buffered solution at pH 7.6 exhibited an intense colorimetric response at a wavelength maximum of 505 nm. The assay exhibited excellent performance characteristics as it revealed a Z’ factor of 0.87 and it has the potential to be further adopted into high-throughput screening studies for therapeutic drug discovery research.
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基于四唑鎓的新型比色法检测 SARS-CoV-2 中的螺旋酶 nsp13
严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)是一种人类致病病毒,其编码的螺旋酶(SC2Hel)对病毒复制至关重要。SC2Hel 能以 NTP 依赖性方式从 5′至 3′方向解开 dsRNA 或 dsDNA。在涉及 SARS-CoV 和 SARS-CoV-2 的研究中,标准的螺旋酶测定依赖于荧光共振能量转移的概念。在此,我们开发了一种新型的基于四唑的比色测定系统,用于检测通过 SC2Hel 活性产生的 ADP。这种 SC2Hel 检测方法结合了三个酶耦合步骤,分别涉及依赖 ADP 的莱特拉热球菌葡萄糖激酶(TlGlcK)、介根芽孢杆菌葡萄糖-6-磷酸脱氢酶(LmG6PDH)和克鲁维氏梭菌二磷酸盐酶(CkDIA)。碘硝基氯化四氮唑(INT)是一种比色四氮唑试剂,用于检测的最后一步,在还原过程中转化为 INT-formazan。在 pH 值为 7.6 的缓冲溶液中,INT-formazan 在波长最大值 505 纳米处显示出强烈的比色反应。该检测方法的 Z'因子为 0.87,表现出卓越的性能特征,有望进一步应用于治疗药物发现研究的高通量筛选研究中。
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