Shelef Omri, Gutkin Sara, Nassir Molhm, Krinsky Anne, Satchi-Fainaro Ronit, Baran Phil S, Shabat Doron
School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel-Aviv University, Tel Aviv 69978, Israel.
Department of Chemistry, Scripps Research, La Jolla, California 92037, United States.
Bioconjug Chem. 2025 Feb 19;36(2):152-159. doi: 10.1021/acs.bioconjchem.4c00454. Epub 2025 Jan 9.
ENPP-1 is a transmembrane enzyme involved in nucleotide metabolism, and its overexpression is associated with various cancers, making it a potential therapeutic target and biomarker for early tumor diagnosis. Current detection methods for ENPP-1 utilize a colorimetric probe, , which has significant limitations in sensitivity. Here, we present probe , the first nucleic acid-based chemiluminescent probe designed for rapid and highly sensitive detection of ENPP-1 activity. The design of probe features a phenoxy-adamantyl-1,2-dioxetane luminophore linked to thymidine via a phosphodiesteric bond. Upon cleavage of the enzymatic substrate by ENPP-1, the probe undergoes an efficient chemiexcitation process to emit a green photon. Probe demonstrates an exceptional signal-to-noise ratio of 15000 and a limit of detection value approximately 4500-fold lower than the widely used colorimetric probe . A comparison of activation by ENPP-1 versus alkaline phosphatase (ALP) reveals a complete lack of selectivity. Removal of the self-immolative spacer from probe resulted in a new chemiluminescent probe, , with an 18.4-fold increase in selectivity for ENPP-1 over ALP. The ability of probe to detect ENPP-1 activity in mammalian cells was assessed using the human breast cancer cell line MDA-MB-231. This probe demonstrated a 19.5-fold improvement in the signal-to-noise ratio, highlighting its superior ability to detect ENPP-1 activity in a biological sample. As far as we know, to date, and are the most sensitive probes for the detection of ENPP-1 catalytic activity. We anticipate that our new chemiluminescent probes will be valuable for various applications requiring ENPP-1 detection, including enzyme inhibitor-based drug discovery assays. The insights gained from our probe design principles could advance the development of more selective probes for ENPP-1 and contribute to future innovations in chemiluminescence research.
ENPP-1是一种参与核苷酸代谢的跨膜酶,其过表达与多种癌症相关,使其成为早期肿瘤诊断的潜在治疗靶点和生物标志物。目前用于检测ENPP-1的方法使用比色探针,但其在灵敏度方面存在显著局限性。在此,我们展示了探针,这是首个基于核酸的化学发光探针,设计用于快速且高度灵敏地检测ENPP-1活性。探针的设计特点是通过磷酸二酯键将苯氧基-金刚烷基-1,2-二氧杂环丁烷发光团与胸苷相连。当ENPP-1切割酶底物时,探针会经历高效的化学激发过程以发射绿色光子。探针展示出15000的出色信噪比,检测限比广泛使用的比色探针低约4500倍。比较ENPP-1与碱性磷酸酶(ALP)对的激活情况发现完全缺乏选择性。从探针上去除自毁间隔基产生了一种新的化学发光探针,其对ENPP-1相对于ALP的选择性提高了18.4倍。使用人乳腺癌细胞系MDA-MB-231评估了探针在哺乳动物细胞中检测ENPP-1活性的能力。该探针在信噪比方面提高了19.5倍,突出了其在生物样品中检测ENPP-1活性的卓越能力。据我们所知,迄今为止,和是检测ENPP-1催化活性最灵敏的探针。我们预计我们的新型化学发光探针对于需要检测ENPP-1的各种应用将具有价值,包括基于酶抑制剂的药物发现测定。从我们的探针设计原则中获得的见解可能会推动开发更具选择性的ENPP-1探针,并为化学发光研究的未来创新做出贡献。