Molecular Engineering of Self-Immolative Bioresponsive MR Probes

被引:23
|
作者
Tang, Jian-Hong [1 ]
Li, Hao [1 ]
Yuan, Chaonan [1 ]
Parigi, Giacomo [2 ,3 ,4 ]
Luchinat, Claudio [2 ,3 ,4 ]
Meade, Thomas J. [1 ]
机构
[1] Northwestern Univ, Dept Chem Mol Biosci Neurobiol & Physiol & Radiol, Evanston, IL 60208 USA
[2] Univ Florence, Dept Chem, I-50019 Sesto Fiorentino, Italy
[3] Univ Florence, Magnet Resonance Ctr CERM, I-50019 Sesto Fiorentino, Italy
[4] Consorzio Interuniv Risonanze Magnet Met Prot CIRM, I-50019 Sesto Fiorentino, Italy
基金
美国国家卫生研究院;
关键词
CONTRAST AGENT; BETA-GALACTOSIDASE; RELAXATION; TRACKING; ENZYMES;
D O I
10.1021/jacs.2c13672
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Real-time detection of bio-event in whole animals provides essential information for understanding biological and therapeutic processes. Magnetic resonance (MR) imaging represents a non-invasive approach to generating three-dimensional anatomic images with high spatial-temporal resolution and unlimited depth penetration. We have developed several self-immolative enzyme-activatable agents that provide excellent in vivo contrast and function as gene expression reporters. Here, we describe a vast improvement in image contrast over our previous generations of these bioresponsive agents based on a new pyridyl-carbamate Gd(III) complex. The pyridyl-carbamate-based agent has a very low MR relaxivity in the "off -state" (r1 = 1.8 mM-1 s-1 at 1.41 T). However, upon enzymatic processing, it generates a significantly higher relaxivity with a Delta r1= 106% versus Delta r1 similar to 20% reported previously. Single X-ray crystal and nuclear magnetic relaxation dispersion analyses offer mechanistic insights regarding MR signal enhancement at the molecular scale. This work demonstrates a pyridyl-carbamate-based self-immolative molecular platform for the construction of enzymatic bio-responsive MR agents, which can be adapted to a wide range of other targets for exploring stimuli-responsive materials and biomedical applications.
引用
收藏
页码:10045 / 10050
页数:6
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