Bolarinho Rylie, Yin Jiaze, Ni Hongli, Xia Qing, Cheng Ji-Xin
Department of Chemistry, Boston University, Boston, Massachusetts 02215, United States.
Department of Electrical and Computer Engineering, Boston University, Boston, Massachusetts 02215, United States.
Anal Chem. 2025 Mar 4;97(8):4299-4307. doi: 10.1021/acs.analchem.4c03689. Epub 2025 Feb 18.
Mid-infrared photothermal (MIP) microscopy is an emerging tool for biological imaging, offering high sensitivity, subcellular resolution, and rapid image acquisition. However, the MIP signal of low concentration molecules in biological systems is often hindered or masked by background absorption, largely contributed by water, resulting from the H-O-H scissors-bending band in the fingerprint window or the bend-libration combination band in the cell-silent window. To preserve all desired signals while suppressing the background, we report a single-shot time-resolved MIP measurement that allows differentiation between the background and analyte signal based on their distinct photothermal dynamics. The results show that the thermal decay of the background is significantly longer than that of the desired intracellular signal, mainly due to the larger mass and heat capacity of water compared to those of intracellular features. Through two-component exponential fitting, we successfully differentiated and suppressed the background, while preserving the desired intracellular signal in both the fingerprint and cell-silent windows. By leveraging the thermal dynamics differences obtained from a single-shot measurement, we effectively remove the background and enhance the detection of small signals in a biological system.
中红外光热(MIP)显微镜是一种新兴的生物成像工具,具有高灵敏度、亚细胞分辨率和快速图像采集能力。然而,生物系统中低浓度分子的MIP信号常常受到背景吸收的阻碍或掩盖,背景吸收主要由水引起,这是由于指纹窗口中的H-O-H剪刀弯曲带或细胞沉默窗口中的弯曲-振动组合带所致。为了在抑制背景的同时保留所有所需信号,我们报告了一种单次时间分辨MIP测量方法,该方法能够根据背景和分析物信号不同的光热动力学来区分它们。结果表明,背景的热衰减明显长于所需的细胞内信号,这主要是因为与细胞内特征相比,水的质量和热容量更大。通过双组分指数拟合,我们成功地区分并抑制了背景,同时在指纹窗口和细胞沉默窗口中都保留了所需的细胞内信号。通过利用单次测量获得的热动力学差异,我们有效地去除了背景并增强了生物系统中小信号的检测。