纳米颗粒
顺磁性
旋转相关时间
离解常数
电子顺磁共振
核磁共振
化学
金属
荧光
结晶学
材料科学
纳米技术
生物化学
物理
受体
有机化学
量子力学
作者
Mark Allen,Jeff W. M. Bulte,Lars Liepold,Gautam Basu,Holly A. Zywicke,Joseph A. Frank,Mark Young,Trevor Douglas
摘要
Abstract In order to compensate for the inherent high threshold of detectability of MR contrast agents, there has been an active interest in the development of paramagnetic nanoparticles incorporating high payloads of Gd 3+ with high molecular relaxivities. Toward this end, the protein cage of Cowpea chlorotic mottle virus (CCMV), having 180 metal binding sites, is being explored. In vivo CCMV binds Ca 2+ at specific metal binding sites; however, Gd 3+ can also bind at these sites. Using fluorescence resonance energy transfer we have characterized the binding affinity of Gd 3+ to the metal binding sites by competition experiments with Tb 3+ . The measured dissociation constant ( K d ) for Gd 3+ bound to the virus is 31 μM. The T 1 and T 2 relaxivities of solvent water protons in the presence of Gd 3+ ‐bound CCMV were 202 and 376 mM −1 s −1 , respectively, at 61 MHz Larmor frequency. The unusually high relaxivity values of the Gd 3+ –CCMV are largely a result of the nanoparticle virus size and the large number of Gd 3+ ions bound to the virus. These preliminary results should encourage further investigations into the use of viral protein cages as a new platform for MR contrast agents. Magn Reson Med, 2005. Published 2005 Wiley‐Liss, Inc.
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