Wang Ruogu, Feng Yunlong, Valm Alex M
Department of Biology, University at Albany, SUNY, 1400 Washington Ave, Albany, NY 12222, United States.
RNA Institute, University at Albany, SUNY, 1400 Washington Ave, Albany, NY 12222, United States.
Brief Bioinform. 2024 Nov 22;26(1). doi: 10.1093/bib/bbaf005.
The accuracy of assigning fluorophore identity and abundance, known as spectral unmixing, in biological fluorescence microscopy images remains a significant challenge due to the substantial overlap in emission spectra among fluorophores. In traditional laser scanning confocal spectral microscopy, fluorophore information is acquired by recording emission spectra with a single combination of discrete excitation wavelengths. However, organic fluorophores possess characteristic excitation spectra in addition to their unique emission spectral signatures. In this paper, we propose a generalized multi-view machine learning approach that leverages both excitation and emission spectra to significantly improve the accuracy in differentiating multiple highly overlapping fluorophores in a single image. By recording emission spectra of the same field with multiple combinations of excitation wavelengths, we obtain data representing different views of the underlying fluorophore distribution in the sample. We then propose a multi-view machine learning framework that allows for the flexible incorporation of noise information and abundance constraints, enabling the extraction of spectral signatures from reference images and efficient recovery of corresponding abundances in unknown mixed images. Numerical experiments on simulated image data demonstrate the method's efficacy in improving accuracy, allowing for the discrimination of 100 fluorophores with highly overlapping spectra. Furthermore, validation on images of mixtures of fluorescently labeled Escherichia coli highlights the power of the proposed multi-view strategy in discriminating fluorophores with spectral overlap in real biological images.
在生物荧光显微镜图像中,确定荧光团的身份和丰度(即光谱解混)的准确性仍然是一项重大挑战,因为荧光团之间的发射光谱存在大量重叠。在传统的激光扫描共聚焦光谱显微镜中,通过用离散激发波长的单一组合记录发射光谱来获取荧光团信息。然而,有机荧光团除了具有独特的发射光谱特征外,还具有特征激发光谱。在本文中,我们提出了一种广义多视图机器学习方法,该方法利用激发光谱和发射光谱来显著提高在单个图像中区分多个高度重叠荧光团的准确性。通过用多种激发波长组合记录同一场景的发射光谱,我们获得了表示样品中潜在荧光团分布不同视图的数据。然后,我们提出了一个多视图机器学习框架,该框架允许灵活纳入噪声信息和丰度约束,从而能够从参考图像中提取光谱特征,并在未知混合图像中高效恢复相应的丰度。对模拟图像数据的数值实验证明了该方法在提高准确性方面的有效性,能够区分光谱高度重叠的100种荧光团。此外,对荧光标记大肠杆菌混合物图像的验证突出了所提出的多视图策略在区分真实生物图像中具有光谱重叠的荧光团方面的能力。