Plasmon-enhanced stimulated Raman scattering microscopy with single-molecule detection sensitivity

被引:115
作者
Zong, Cheng [1 ,2 ]
Premasiri, Ranjith [3 ,4 ]
Lin, Haonan [1 ]
Huang, Yimin [3 ]
Zhang, Chi [1 ]
Yang, Chen [3 ,4 ]
Ren, Bin [2 ]
Ziegler, Lawrence D. [3 ,4 ]
Cheng, Ji-Xin [1 ,3 ,4 ]
机构
[1] Boston Univ, Dept Biomed Engn, Dept Elect & Comp Engn, Boston, MA 02215 USA
[2] Xiamen Univ, Collaborat Innovat Ctr Chem Energy Mat, MOE Key Lab Spectrochem Anal & Instrumentat, Coll Chem & Chem Engn,State Key Lab Phys Chem Sol, Xiamen 361005, Fujian, Peoples R China
[3] Boston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
[4] Boston Univ, Photon Ctr, Boston, MA 02215 USA
关键词
IN-VIVO; SPECTROSCOPY; PROOF; SERS;
D O I
10.1038/s41467-019-13230-1
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
Stimulated Raman scattering (SRS) microscopy allows for high-speed label-free chemical imaging of biomedical systems. The imaging sensitivity of SRS microscopy is limited to similar to 10mM for endogenous biomolecules. Electronic pre-resonant SRS allows detection of sub-micromolar chromophores. However, label-free SRS detection of single biomolecules having extremely small Raman cross-sections (similar to 10(-30) cm(2) sr(-1)) remains unreachable. Here, we demonstrate plasmon-enhanced stimulated Raman scattering (PESRS) microscopy with single-molecule detection sensitivity. Incorporating pico-Joule laser excitation, background subtraction, and a denoising algorithm, we obtain robust single-pixel SRS spectra exhibiting single-molecule events, verified by using two isotopologues of adenine and further confirmed by digital blinking and bleaching in the temporal domain. To demonstrate the capability of PESRS for biological applications, we utilize PESRS to map adenine released from bacteria due to starvation stress. PESRS microscopy holds the promise for ultrasensitive detection and rapid mapping of molecular events in chemical and biomedical systems.
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页数:11
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