An In Vivo Spectral Multiplexing Approach for the Cooperative Imaging of Different Disease-Related Biomarkers with Near-Infrared Fluorescent Förster Resonance Energy Transfer Probes

In recent years, much progress has been made in analyzing the molecular origin of many diseases in vivo. For most applications, attention has been devoted to the detection of single molecules only. In this study, we present a proof of concept for the straightforward monitoring of interactions between different molecules via Förster resonance energy transfer (FRET) in an in vivo spectral multiplexing approach using conventional small organic dyes covalently attached to antibodies. Methods: We coupled the fluorophores DY-682 (donor; absorption [abs]/emission [em], 674/712 nm), DY-505 (control donor; abs/em, 498/529 nm), and DY-782 (acceptor; abs/em, 752/795 nm) to the model antibody IgG. The occurrence of FRET between these fluorophores was assessed in vitro for conjugate mixtures adsorbed onto membranes, after accumulation into the phagocytic compartment of macrophages (J774 cells), and in vivo in a mouse edema model using a whole-body animal imaging system with multispectral analysis features. Results: When the free acceptor DY-782 was combined with the DY-682 donor, FRET occurred as a consequence of small dye-to-dye distances, unlike the case for mixtures of the dyes DY-782 and DY-505. Our proof of concept was also transferred to living cells after internalization of the DY-682-IgG–DY-782-IgG pair into macrophages and finally to animals, where intermolecular FRET was observed after systemic probe application in vivo in edema-bearing mice. Conclusion: Our simple cooperative-imaging approach enables the noninvasive detection of the presence of two or principally even more neighboring disease-related biomarkers. This finding is of high relevance for the in vivo identification of complex biologic processes requiring strong spatial interrelations of target molecules in key pathologic activation processes such as inflammation, cancer, and neurodegenerative diseases.

[1]  L. Chodosh,et al.  Preparation and Characterization of l-[5-11C]-Glutamine for Metabolic Imaging of Tumors , 2012, The Journal of Nuclear Medicine.

[2]  M. Grabolle,et al.  Comparison of methods and achievable uncertainties for the relative and absolute measurement of photoluminescence quantum yields. , 2011, Analytical chemistry.

[3]  S. John,et al.  Subcellular Localization of Hexokinases I and II Directs the Metabolic Fate of Glucose , 2011, PloS one.

[4]  A. Savitsky,et al.  Fluorescence resonance energy transfer between fluorescent proteins as powerful toolkits for in vivo studies , 2011 .

[5]  Sha Jin,et al.  A glucose sensor protein for continuous glucose monitoring. , 2010, Biosensors & bioelectronics.

[6]  Ilya V Turchin,et al.  Lifetime imaging of FRET between red fluorescent proteins , 2010, Journal of biophotonics.

[7]  L. Vinokurov,et al.  Genetically encoded FRET-pair on the basis of terbium-binding peptide and red fluorescent protein , 2010, Applied Biochemistry and Microbiology.

[8]  W. Kaiser,et al.  Novel Fluorophores as Building Blocks for Optical Probes for In Vivo Near Infrared Fluorescence (NIRF) Imaging , 2010, Journal of Fluorescence.

[9]  W. Heindel,et al.  In Vivo Optical Imaging of Cellular Inflammatory Response in Granuloma Formation Using Fluorescence-Labeled Macrophages , 2009, Journal of Nuclear Medicine.

[10]  W. Kaiser,et al.  An in vitro characterization study of new near infrared dyes for molecular imaging. , 2009, European journal of medicinal chemistry.

[11]  P. Libby,et al.  Identification of Splenic Reservoir Monocytes and Their Deployment to Inflammatory Sites , 2009, Science.

[12]  I. Gryczynski,et al.  Near-infrared squaraine dyes for fluorescence enhanced surface assay. , 2009, Dyes and pigments : an international journal.

[13]  Clifford Hoyt,et al.  Visualization of Microscopy‐Based Spectral Imaging Data from Multi‐Label Tissue Sections , 2008, Current protocols in molecular biology.

[14]  R. Nitschke,et al.  Quantum dots versus organic dyes as fluorescent labels , 2008, Nature Methods.

[15]  W. Kaiser,et al.  Fluorescent liposomes as contrast agents for in vivo optical imaging of edemas in mice. , 2008, Small.

[16]  W. Kaiser,et al.  In vivo near-infrared fluorescence imaging of carcinoembryonic antigen-expressing tumor cells in mice. , 2008, Radiology.

[17]  Igor L. Medintz,et al.  Materials for fluorescence resonance energy transfer analysis: beyond traditional donor-acceptor combinations. , 2006, Angewandte Chemie.

[18]  R. A. Ezekowitz,et al.  Phagocytosis: elegant complexity. , 2005, Immunity.

[19]  K. Rurack,et al.  Traceability in Fluorometry: Part II. Spectral Fluorescence Standards , 2005, Journal of Fluorescence.

[20]  Vasilis Ntziachristos,et al.  Looking and listening to light: the evolution of whole-body photonic imaging , 2005, Nature Biotechnology.

[21]  Mark H Ellisman,et al.  A FlAsH-based FRET approach to determine G protein–coupled receptor activation in living cells , 2005, Nature Methods.

[22]  Daniel L. Farkas,et al.  Tumor labeling in vivo using cyanine-conjugated monoclonal antibodies , 1995, Cancer Immunology, Immunotherapy.

[23]  François Mach,et al.  Inflammation and Atherosclerosis , 2004, Herz.

[24]  Jonathan Cohen The immunopathogenesis of sepsis , 2002, Nature.

[25]  Marcus Fehr,et al.  Visualization of maltose uptake in living yeast cells by fluorescent nanosensors , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[26]  K. Licha Contrast Agents for Optical Imaging , 2002 .

[27]  M. Pawlikowski,et al.  Anti-Inflammatory Effects of Somatostatin Analogs on Zymosan-Induced Earlobe Inflammation in Mice: Comparison with Dexamethasone and Ketoprofen , 2001, Neuroimmunomodulation.

[28]  M. Perretti,et al.  Regulation of macrophage inflammatory protein-1 alpha expression and function by endogenous interleukin-10 in a model of acute inflammation. , 1999, Biochemical and biophysical research communications.

[29]  A. Waggoner,et al.  Cyanine-labeling reagents: sulfobenzindocyanine succinimidyl esters. , 1996, Bioconjugate chemistry.

[30]  M. Chalfie GREEN FLUORESCENT PROTEIN , 1995, Photochemistry and photobiology.

[31]  Douglas C. Youvan,et al.  Red-Shifted Excitation Mutants of the Green Fluorescent Protein , 1995, Bio/Technology.

[32]  H. Heymann Methoden der Organischen Chemie , 1956 .

[33]  C. R. Noller Methoden der organischen Chemie. , 1954 .