通过酶促分子原位自组装实现智能分子成像和抗肿瘤探针

JACS Au Pub Date : 2024-07-03 DOI:10.1021/jacsau.4c00392
Xidan Wen, Chao Zhang, Yuyang Tian, Yinxing Miao, Shaohai Liu, Jing-Juan Xu, Deju Ye, Jian He
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引用次数: 0

摘要

酶促分子原位自组装(E-MISA)可使合成小分子在活体内合成高阶纳米结构,已成为分子成像和治疗学的一种前景广阔的策略。这种策略利用酶的催化活性触发探针底物的原位转换和组装,从而延长探针在靶细胞或组织中的保留时间并聚集许多探针分子。通过对特定酶做出反应,可增强成像信号或治疗功能。这种 E-MISA 策略已成功应用于开发酶激活智能分子成像或治疗探针的体内应用。在本视角中,我们将讨论用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 "成像和治疗探针的应用。最后,我们讨论了目前利用 E-MISA 战略进行疾病诊断和治疗,特别是临床转化所面临的挑战和前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Smart Molecular Imaging and Theranostic Probes by Enzymatic Molecular In Situ Self-Assembly

Smart Molecular Imaging and Theranostic Probes by Enzymatic Molecular In Situ Self-Assembly
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.
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