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本文引用的文献

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Widespread genetic heterogeneity in multiple myeloma: implications for targeted therapy.多发性骨髓瘤的广泛遗传异质性:对靶向治疗的影响。
Cancer Cell. 2014 Jan 13;25(1):91-101. doi: 10.1016/j.ccr.2013.12.015.
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Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma.突变分析揭示了复发性神经胶质瘤的起源和治疗驱动的进化。
Science. 2014 Jan 10;343(6167):189-193. doi: 10.1126/science.1239947. Epub 2013 Dec 12.
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Immunogold cytochemistry in neuroscience.神经科学中的免疫胶体金细胞化学。
Nat Neurosci. 2013 Jul;16(7):798-804. doi: 10.1038/nn.3418. Epub 2013 Jun 25.
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Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics.人类胶质母细胞瘤的肿瘤内异质性反映了癌症进化动态。
Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):4009-14. doi: 10.1073/pnas.1219747110. Epub 2013 Feb 14.
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Seven-color fluorescence imaging of tissue samples based on Fourier spectroscopy and singular value decomposition.基于傅里叶光谱和奇异值分解的组织样本七色荧光成像。
J Histochem Cytochem. 2000 May;48(5):653-62. doi: 10.1177/002215540004800509.
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Three-dimensional structure of the Fab' fragment of a human immunoglobulin at 2,8-A resolution.人免疫球蛋白Fab'片段在2.8埃分辨率下的三维结构。
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8
Evaluation of IgG molecules, Fab' fragments and IgG-horseradish peroxidase conjugates as surface labels for freeze-etched membranes.评估IgG分子、Fab'片段和IgG-辣根过氧化物酶缀合物作为冷冻蚀刻膜表面标记物的性能。
J Microsc. 1979 Dec;117(3):363-73. doi: 10.1111/j.1365-2818.1979.tb04693.x.

通过组合标记在抗体上创建复杂的荧光团光谱

Creating Complex Fluorophore Spectra on Antibodies Through Combinatorial Labeling.

作者信息

Holzapfel Hadassa Y, Birtwistle Marc R

机构信息

Department of Pharmacology and Systems Therapeutics | Icahn School of Medicine at Mount Sinai | New York, NY, USA.

出版信息

Transl Sci. 2016 Mar;2(3). Epub 2016 Mar 31.

PMID:27284574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4896637/
Abstract

Fluorescently-labeled antibodies are central to many biochemical assays, but they are not easy to multiplex beyond 3-4 colors. A long-term hypothesis of ours is that labeling antibodies with multiple fluorophores, in a way such that fluorescence resonance energy transfer (FRET) occurs, may provide a way to increase fluorescence multiplexing ability by creating a rich variety of complex emission spectra that could be deconvolved via spectral methods. However, it is not yet clear how one can effectively label antibodies with multiple fluorophores that exhibit FRET. Here, we show how to use Mix-n-Stain antibody labeling kits from Biotium to label antibodies with multiple fluorophores that exhibit FRET. Key to our approach is the use of Fab fragments, as opposed to full IgG molecules, since the full IgG molecules are generally too large to allow the fluorophore proximity necessary for observable FRET. We show that our approach works with two different sets of FRET-capable fluorophore combinations: CF405M/CF488A and CF568/CF640R. These results form the basis for continued development of approaches for increased multiplexing of fluorescent antibody measurements.

摘要

荧光标记抗体是许多生化检测的核心,但要实现超过3 - 4种颜色的多重检测并不容易。我们长期以来的一个假设是,以一种能发生荧光共振能量转移(FRET)的方式用多种荧光团标记抗体,可能会通过创建丰富多样的复杂发射光谱来提供一种提高荧光多重检测能力的方法,这些光谱可通过光谱方法进行解卷积。然而,目前尚不清楚如何用能表现出FRET的多种荧光团有效地标记抗体。在这里,我们展示了如何使用Biotium公司的Mix - n - Stain抗体标记试剂盒,用能表现出FRET的多种荧光团来标记抗体。我们方法的关键在于使用Fab片段,而不是完整的IgG分子,因为完整的IgG分子通常太大,无法实现可观察到FRET所需的荧光团接近程度。我们表明我们的方法适用于两组不同的具有FRET能力的荧光团组合:CF405M/CF488A和CF568/CF640R。这些结果为持续开发增加荧光抗体检测多重性的方法奠定了基础。