Activatable and Cell-Penetrable Multiplex FRET Nanosensor for Profiling MT1-MMP Activity in Single Cancer Cells

被引:43
作者
Chung, Eddie Y. [1 ,2 ]
Ochs, Christopher J. [3 ]
Wang, Yi [4 ]
Lei, Lei [1 ,2 ,4 ]
Qin, Qin [1 ,2 ]
Smith, Andrew M. [4 ]
Strongin, Alex Y. [5 ]
Kamm, Roger [3 ]
Qi, Ying-Xin [6 ]
Lu, Shaoying [1 ,2 ,4 ]
Wang, Yingxiao [1 ,2 ,4 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Inst Engn Med, La Jolla, CA 92093 USA
[3] Singapore MIT Alliance Res & Technol, BioSyst & Micromech, Singapore 138602, Singapore
[4] Univ Illinois, Dept Bioengn, Champaign, IL 61801 USA
[5] Sanford Burnham Med Res Inst, La Jolla, CA 92037 USA
[6] Shanghai Jiao Tong Univ, Inst Mechanobiol & Med Engn, Shanghai 200240, Peoples R China
关键词
activatable cell-penetrating peptide; multiplex signals; FRET nanosensor; MT1-MMP; single cell; cancer; TYPE-1; MATRIX-METALLOPROTEINASE; QUANTUM DOTS; IN-VIVO; INTEGRIN ALPHA-V-BETA-3; PROTEOLYTIC ACTIVITY; INVASION PROGRAMS; INHIBITION; PEPTIDES; DELIVERY; MICE;
D O I
10.1021/acs.nanolett.5b01047
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed a quantum-dot-based fluorescence resonance energy transfer (QD-FRET) nanosensor to visualize the activity of matrix metalloproteinase (MT1-MMP) at cell membrane. A bended peptide with multiple motifs was engineered to position the FRET pair at a close proximity to allow energy transfer, which can be cleaved by active MT1-MMP to result in FRET changes and the exposure of cell penetrating sequence. Via FRET and penetrated QD signals, the nanosensor can profile cancer cells.
引用
收藏
页码:5025 / 5032
页数:8
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