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Weldon School of Biomedical Engineering and Department of Chemistry, Purdue University, West Lafayette, Indiana 47907
Correspondence: Address reprint requests to Ji-Xin Cheng, Weldon School of Biomedical Engineering and Dept. of Chemistry, Purdue University, West Lafayette, IN 47907. Tel.: 765-494-4335; Fax: 765-494-1193; E-mail: jcheng{at}purdue.edu.
We demonstrate quantitative vibrational imaging of specific lipid molecules in single bilayers using laser-scanning coherent anti-Stokes Raman scattering (CARS) microscopy with a lateral resolution of 0.25 µm. A lipid is spectrally separated from other molecules by using deuterated acyl chains that provide a large CARS signal from the symmetric CD2 stretch vibration around 2100 cm1. Our temperature control experiments show that d62-DPPC has similar bilayer phase segregation property as DPPC when mixing with DOPC. By using epi-detection and optimizing excitation and detection conditions, we are able to generate a clear vibrational contrast from d62-DPPC of 10% molar fraction in a single bilayer of DPPC/d62-DPPC mixture. We have developed and experimentally verified an image analysis model that can derive the relative molecular concentration from the difference of the two CARS intensities measured at the peak and dip frequencies of a CARS band. With the above strategies, we have measured the molar density of d62-DPPC in the coexisting domains inside the DOPC/d62-DPPC (1:1) supported bilayers incorporated with 040% cholesterol. The observed interesting changes of phospholipid organization upon addition of cholesterol to the bilayer are discussed.
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