Source: Raghu, D. et al., A Label-free Technique for the Spatio-temporal Imaging of Single Cell Secretions. J. Vis. Exp. (2015)
This video demonstrates localized surface plasmon resonance imaging to detect protein secretions from a single cell. Using a microfluidic setup and a peptide-bound plasmonic nanostructure chip, changes in reflected light intensity at the resonance angle reveal interactions with secreted proteins from a single cell.
1. Nanostructure Fabrication
2. Chip Cleaning and Application of Self-assembled Monolayer
3. Surface Functionalization and Kinetic Characterization
Note: Use the functionalized chip in the commercial SPR instrument to characterize the kinetic rate constants between the ligand and the analyte, as well as to study the resistance of SAM to non-specific binding. There is a wide range of flow rates and microfluidic designs that allow for efficient surface functionalization. Since we have a commercially available SPR we standardized around its recommended flow rates. We note that these flow rates are typical of all SPR instruments and so are not restrictive. The SPR instrument is not a necessity since all functionalization can be done directly on the localized surface plasmon resonance imaging (LSPR) chip, but it did reduce our workload because it is a multiplexed instrument whereas our LSPR microfluidic setup is not.
4. LSPR General Settings
5. LSPR Imaging of Anti-c-myc Secretions from 9E10 Hybridoma Cells
Note: The hybridoma cell line used for this study express anti-c-myc antibody constitutively and hence do not require a chemical trigger
Figure 1. Optical Setup. The illuminated light from a halogen lamp is first filtered by a long pass filter (LP). The light is linearly polarized (P1) and illuminates the sample via a 40X/1.4 NA objective. The scattered light is collected by the objective and passed through a crossed polarizer (P2). A 50/50 beam splitter (BS) is inserted into the collected light path for simultaneous spectroscopic and imagery analysis. Top Right: An atomic force microscopy image of 9 individual nanostructures separated by a pitch of 300 nm.
The authors have nothing to disclose.
25mm diameter glass coverslips | Bioscience Tools | CSHP-No1.5-25 | 170±5 µm is optimal |
Poly-methyl methacrylate | Microchem | PMMA 950 A4 | |
Ethyl lactate methyl metacrylate | Microchem | MMA EL6 | |
Electron beam evaporator | Temescal | FC-2000 | |
Electron beam lithography | Raith | Series 150 | |
Ethanol | Sigma-Aldrich | 459836 | |
Acetone | Sigma-Aldrich | 320110 | |
CR-7 chromium etchant | Cyantek | CR-7 | |
Scanning electron microscope | Zeiss | Ultra 55 | |
Atomic force microscope | Veeco | Nanoscope III | |
Plasma ashing system | Technics | Series 85 RIE | |
SH-(CH2)8-EG3-OH (SPO) | Prochimia | TH 001-m8.n3-0.2 | |
SH-(CH2)11-EG3-COOH (SPC) | Prochimia | TH 003m11n3-0.1 | |
SH-(CH2)11-EG3-NH2 (SPN) | Prochimia | TH 002-m11.n3-0.2 | |
Surface plasmon resonance system | Biorad | XPR36 | |
Bare gold chip | Biorad | GLC chip | Plasma ashed to remove the monolayer |
1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide | Thermo | 22980 | |
N-hydroxysuccinimide (NHS) | Thermo | 24510 | |
Pentylamine-Biotin | Thermo | 21345 | |
Ethanolamine | Sigma-Aldrich | E9508 | |
Neutraavidin | Thermo | 31000 | |
Phosphate buffered saline | Thermo | 28374 | |
Tween 20 | Sigma-Aldrich | P2287 | |
Inverted microscope | Zeiss | Axio Observer | Microscope is equipped with 40X oil immersion objective; CO2 and humidity incubation from Pecon GmbH |
CCD camera | Hamamatsu | Orca R2 | Thermoelectrically cooled (16 bit) |
Spectrometer | Ocean Optics | QE65Pro | |
Spectrasuite | Ocean Optics | version1.4 | |
c-myc peptide HyNic Tag | Solulink | SP-E003 | |
monoclonal anti-c-myc antibody | Sigma-Aldrich | M4439 | |
Hybridoma cell line | ATCC | CRL-1729 | |
Antibiotic Antimycotic Solution (100×) | Sigma-Aldrich | A5955 | |
Serum free media RPMI 1640 | Invitrogen | 11835-030 | |
Fetal bovine serum | ATCC | 30-2020 | |
Rhodamine DHPE | Life Technologies | L-1392 |