费斯特共振能量转移
荧光
化学
生物传感器
糜蛋白酶
纳米技术
组合化学
材料科学
酶
生物化学
胰蛋白酶
物理
量子力学
作者
Swadesh Kumar Gupta,Priyanka Priyanka,Sai Kiran Mavileti,Shyam S. Pandey,Tamaki Kato
出处
期刊:Molecules
[MDPI AG]
日期:2024-03-14
卷期号:29 (6): 1282-1282
标识
DOI:10.3390/molecules29061282
摘要
Chymotrypsin, a crucial enzyme in human digestion, catalyzes the breakdown of milk proteins, underscoring its significance in both health diagnostics and dairy quality assurance. Addressing the critical need for rapid, cost-effective detection methods, we introduce a groundbreaking approach utilizing far-red technology and HOMO-Förster resonance energy transfer (FRET). Our novel probe, SQ-122 PC, features a unique molecular design that includes a squaraine dye (SQ), a peptide linker, and SQ moieties synthesized through solid-phase peptide synthesis. Demonstrating a remarkable quenching efficiency of 93.75% in a tailored H2O:DMSO (7:3) solvent system, our probe exhibits absorption and emission properties within the far-red spectrum, with an unprecedented detection limit of 0.130 nM. Importantly, our method offers unparalleled selectivity towards chymotrypsin, ensuring robust and accurate enzyme detection. This pioneering work underscores the immense potential of far-red-based homo-FRET systems in enabling the sensitive and specific detection of chymotrypsin enzyme activity. By bridging the gap between cutting-edge technology and biomedical diagnostics, our findings herald a new era of enzyme sensing, promising transformative advancements in disease diagnosis and dairy quality control.
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