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
相关论文
共 50 条
[1]   Nanocrystal targeting in vivo [J].
Åkerman, ME ;
Chan, WCW ;
Laakkonen, P ;
Bhatia, SN ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12617-12621
[2]  
Algar W. R., 2012, ACS NANO, P11044
[3]   Quantum dots as cellular probes [J].
Alivisatos, AP ;
Gu, WW ;
Larabell, C .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2005, 7 :55-76
[4]   Loss of collagenase-2 confers increased skin tumor susceptibility to male mice [J].
Balbín, M ;
Fueyo, A ;
Tester, AM ;
Pendás, AM ;
Pitiot, AS ;
Astudillo, A ;
Overall, CM ;
Shapiro, SD ;
López-Otín, C .
NATURE GENETICS, 2003, 35 (03) :252-257
[5]   Noninvasive imaging of quantum dots in mice [J].
Ballou, B ;
Lagerholm, BC ;
Ernst, LA ;
Bruchez, MP ;
Waggoner, AS .
BIOCONJUGATE CHEMISTRY, 2004, 15 (01) :79-86
[6]   The inactive 44-kDa processed form of membrane type 1 matrix metalloproteinase (MT1-MMP) enhances proteolytic activity via regulation of endocytosis of active MT1-MMP [J].
Cho, Jin-Ah ;
Osenkowski, Pamela ;
Zhao, Huiren ;
Kim, Seaho ;
Toth, Marta ;
Cole, Kristina ;
Aboukameel, Amro ;
Saliganan, Allen ;
Schuger, Lucia ;
Bonfil, R. Daniel ;
Fridman, Rafael .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (25) :17391-17405
[7]   Intracellular delivery of quantum dots for live cell labeling and organelle tracking [J].
Derfus, AM ;
Chan, WCW ;
Bhatia, SN .
ADVANCED MATERIALS, 2004, 16 (12) :961-+
[8]   MT1-MMP initiates activation of pro-MMP-2 and integrin αvβ3 promotes maturation of MMP-2 in breast carcinoma cells [J].
Deryugina, EI ;
Ratnikov, B ;
Monosov, E ;
Postnova, TI ;
DiScipio, R ;
Smith, JW ;
Strongin, AY .
EXPERIMENTAL CELL RESEARCH, 2001, 263 (02) :209-223
[9]   Selective Inhibition of Matrix Metalloproteinase-14 Blocks Tumor Growth, Invasion, and Angiogenesis [J].
Devy, Laetitia ;
Huang, Lili ;
Naa, Laurent ;
Yanamandra, Niranjan ;
Pieters, Henk ;
Frans, Nicolas ;
Chang, Edward ;
Tao, Qingfeng ;
Vanhove, Marc ;
Lejeune, Annabelle ;
van Gool, Reinoud ;
Sexton, Daniel J. ;
Kuang, Guannan ;
Rank, Douglas ;
Hogan, Shannon ;
Pazmany, Csaba ;
Ma, Yu Lu ;
Schoonbroodt, Sonia ;
Nixon, Andrew E. ;
Ladner, Robert C. ;
Hoet, Rene ;
Henderikx, Paula ;
TenHoor, Chris ;
Rabbani, Shafaat A. ;
Valentino, Maria Luisa ;
Wood, Clive R. ;
Dransfield, Daniel T. .
CANCER RESEARCH, 2009, 69 (04) :1517-1526
[10]   In vivo imaging of quantum dots encapsulated in phospholipid micelles [J].
Dubertret, B ;
Skourides, P ;
Norris, DJ ;
Noireaux, V ;
Brivanlou, AH ;
Libchaber, A .
SCIENCE, 2002, 298 (5599) :1759-1762