Continuous imaging of plasmon rulers in live cells reveals early-stage caspase-3 activation at the single-molecule level

被引:168
作者
Jun, Young-Wook [1 ,2 ]
Sheikholeslami, Sassan [1 ,2 ]
Hostetter, Daniel R. [3 ]
Tajon, Cheryl [3 ,4 ]
Craik, Charles S. [3 ,4 ]
Alivisatos, A. Paul [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[3] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
[4] Univ Calif San Francisco, Grad Program Chem & Chem Biol, San Francisco, CA 94158 USA
基金
美国国家卫生研究院;
关键词
caspase; live cell imaging; plasmonic nanoparticles; protease sensor; single-molecule imaging; QUANTUM-DOT BLINKING; APOPTOSIS; RESISTANCE; PARTICLES; DYNAMICS; CLEAVAGE; SURFACE; GOLD;
D O I
10.1073/pnas.0907367106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The use of plasmon coupling in metal nanoparticles has shown great potential for the optical characterization of many biological processes. Recently, we have demonstrated the use of "plasmon rulers'' to observe conformational changes of single biomolecules in vitro. Plasmon rulers provide robust signals without photo-bleaching or blinking. Here, we show the first application of plasmon rulers to in vivo studies to observe very long trajectories of single biomolecules in live cells. We present a unique type of plasmon ruler comprised of peptide-linked gold nanoparticle satellites around a core particle, which was used as a probe to optically follow cell-signaling pathways in vivo at the single-molecule level. These "crown nanoparticle plasmon rulers'' allowed us to continuously monitor trajectories of caspase-3 activity in live cells for over 2 h, providing sufficient time to observe early-stage caspase-3 activation, which was not possible by conventional ensemble analyses.
引用
收藏
页码:17735 / 17740
页数:6
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