Bioengineered Probes for Molecular Magnetic Resonance Imaging in the Nervous System

被引:16
作者
Hsieh, Vivian [2 ]
Jasanoff, Alan [1 ,3 ,4 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[4] MIT, Dept Nucl Sci & Engn, Cambridge, MA 02139 USA
来源
ACS CHEMICAL NEUROSCIENCE | 2012年 / 3卷 / 08期
基金
加拿大自然科学与工程研究理事会;
关键词
Molecular imaging; neuroimaging; contrast agent; central nervous system; protein engineering; BLOOD-BRAIN-BARRIER; MRI CONTRAST AGENTS; IN-VIVO; GENE-EXPRESSION; FOCUSED ULTRASOUND; REPORTER; DISRUPTION; PEPTIDES; PROTEIN; VIRUS;
D O I
10.1021/cn300059r
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of molecular imaging probes has changed the nature of neurobiological research. Some of the most notable successes have involved the use of biological engineering techniques for the creation of fluorescent protein derivatives for optical imaging, but recent work has also led to a number of bioengineered probes for magnetic resonance imaging (MRI), the preeminent technique for noninvasive investigation of brain structure and function. Molecular MRI agents are beginning to be applied for experiments in the nervous system, where they have the potential to bridge from molecular to systems or organismic levels of analysis. Compared with canonical synthetic small molecule agents, biomolecular or semibiosynthetic MRI contrast agents offer special advantages due to their amenability to molecular engineering approaches, their properties in some cases as catalysts, and their specificity in targeting and ligand binding. Here, we discuss an expanding list of instances where biological engineering techniques have aided in the design of MRI contrast agents and reporter systems, examining both advantages and limitations of these types of probes for studies in the central nervous system.
引用
收藏
页码:593 / 602
页数:10
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