Department of Chemical and Biomolecular Engineering, Clemson University, Clemson, South Carolina 29634, United States.
Bioconjug Chem. 2021 Jun 16;32(6):1156-1166. doi: 10.1021/acs.bioconjchem.1c00220. Epub 2021 May 19.
Fluorescent antibodies are a workhorse of biomedical science, but fluorescence multiplexing has been notoriously difficult due to spectral overlap between fluorophores. We recently established proof-of-principal for fluorescence Multiplexing using Spectral Imaging and Combinatorics (MuSIC), which uses combinations of existing fluorophores to create unique spectral signatures for increased multiplexing. However, a method for labeling antibodies with MuSIC probes has not yet been developed. Here, we present a method for labeling antibodies with MuSIC probes. We conjugate a DBCO-Peg5-NHS ester linker to antibodies and a single-stranded DNA "docking strand" to the linker and, finally, hybridize two MuSIC-compatible, fluorescently labeled oligos to the docking strand. We validate the labeling protocol with spin-column purification and absorbance measurements. We demonstrate the approach using (i) Cy3, (ii) Tex615, and (iii) a Cy3-Tex615 combination as three different MuSIC probes attached to three separate batches of antibodies. We created single-, double-, and triple-positive beads that are analogous to single cells by incubating MuSIC probe-labeled antibodies with protein A beads. Spectral flow cytometry experiments demonstrate that each MuSIC probe can be uniquely distinguished, and the fraction of beads in a mixture with different staining patterns are accurately inferred. The approach is general and might be more broadly applied to cell-type profiling or tissue heterogeneity studies in clinical, biomedical, and drug discovery research.
荧光抗体是生物医学科学的得力工具,但由于荧光团之间的光谱重叠,荧光多重检测一直是一个难题。我们最近通过使用光谱成像和组合(MuSIC)的荧光多重检测建立了原理验证,该方法使用现有荧光团的组合为增加多重检测创建独特的光谱特征。然而,尚未开发出用于 MuSIC 探针标记抗体的方法。在这里,我们提出了一种用 MuSIC 探针标记抗体的方法。我们将 DBCO-Peg5-NHS 酯接头连接到抗体上,将单链 DNA“对接链”连接到接头,最后将两个 MuSIC 兼容的荧光标记寡核苷酸杂交到对接链上。我们通过离心柱纯化和吸光度测量验证了标记方案。我们使用(i)Cy3、(ii)Tex615 和(iii)Cy3-Tex615 组合作为三个不同的 MuSIC 探针,分别连接到三个单独批次的抗体上,证明了该方法的有效性。我们通过孵育 MuSIC 探针标记的抗体与蛋白 A 珠来制备单阳性、双阳性和三阳性珠,这些珠类似于单个细胞。光谱流式细胞术实验表明,每个 MuSIC 探针都可以被独特地区分,并且混合物中具有不同染色模式的珠的比例可以被准确推断。该方法具有通用性,可能更广泛地应用于临床、生物医学和药物发现研究中的细胞类型分析或组织异质性研究。