Wen Xidan, Zhang Chao, Tian Yuyang, Miao Yinxing, Liu Shaohai, Xu Jing-Juan, Ye Deju, He Jian
Department of Nuclear Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210008, China.
State Key Laboratory of Analytical Chemistry for Life Science, Chemistry and Biomedicine Innovation Center (ChemBIC), School of Chemistry and Chemical Engineering, Nanjing University, 163 Xianlin Road, Nanjing 210023, China.
JACS Au. 2024 Jul 3;4(7):2426-2450. doi: 10.1021/jacsau.4c00392. eCollection 2024 Jul 22.
Enzymatic molecular in situ self-assembly (E-MISA) that enables the synthesis of high-order nanostructures from synthetic small molecules inside a living subject has emerged as a promising strategy for molecular imaging and theranostics. This strategy leverages the catalytic activity of an enzyme to trigger probe substrate conversion and assembly in situ, permitting prolonging retention and congregating many molecules of probes in the targeted cells or tissues. Enhanced imaging signals or therapeutic functions can be achieved by responding to a specific enzyme. This E-MISA strategy has been successfully applied for the development of enzyme-activated smart molecular imaging or theranostic probes for in vivo applications. In this Perspective, we discuss the general principle of controlling in situ self-assembly of synthetic small molecules by an enzyme and then discuss the applications for the construction of "smart" imaging and theranostic probes against cancers and bacteria. Finally, we discuss the current challenges and perspectives in utilizing the E-MISA strategy for disease diagnoses and therapies, particularly for clinical translation.
酶促分子原位自组装(E-MISA)能够在活体对象内由合成小分子合成高阶纳米结构,已成为分子成像和治疗诊断学领域一种很有前景的策略。该策略利用酶的催化活性触发探针底物的转化和原位组装,从而延长探针在靶细胞或组织中的保留时间并使许多探针分子聚集。通过对特定酶作出响应,可以实现增强的成像信号或治疗功能。这种E-MISA策略已成功应用于开发用于体内应用的酶激活智能分子成像或治疗诊断探针。在这篇展望文章中,我们首先讨论通过酶控制合成小分子原位自组装的一般原理,然后讨论构建针对癌症和细菌的“智能”成像和治疗诊断探针的应用。最后,我们讨论了利用E-MISA策略进行疾病诊断和治疗,特别是临床转化方面目前面临的挑战和前景。