Granzyme B is an attractive target as a biomarker for contributing to improve the treatment with immune checkpoint inhibitor (ICI). In this study, we designed novel In-labeled granzyme B-targeting single-photon emission computed tomography (SPECT) imaging probes, [ In]IDT and [ In]IDAT. Nonradioactive In-labeled granzyme B-targeting compounds ([ In]IDT, [ In]IDAT) showed the affinity for recombinant mouse granzyme B. [ In]IDT and [ In]IDAT were obtained with moderate radiochemical yield and high stability in mouse plasma (>95%). In a biodistribution experiment using tumor-bearing mice, [ In]IDT and [ In]IDAT showed moderate accumulation in tumor. Ex vivo autoradiography (ARG) indicated that the accumulation of radioactivity in tumor was correlated to expression of granzyme B confirmed by the immunohistochemical staining. These results indicated that [ In]IDT and [ In]IDAT showed the basic properties as granzyme B-targeting SPECT probes.
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http://dx.doi.org/10.1002/jlcr.4045 | DOI Listing |
J Labelled Comp Radiopharm
August 2023
Department of Patho-Functional Bioanalysis, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.
Granzyme B is an attractive target as a biomarker for contributing to improve the treatment with immune checkpoint inhibitor (ICI). In this study, we designed novel In-labeled granzyme B-targeting single-photon emission computed tomography (SPECT) imaging probes, [ In]IDT and [ In]IDAT. Nonradioactive In-labeled granzyme B-targeting compounds ([ In]IDT, [ In]IDAT) showed the affinity for recombinant mouse granzyme B.
View Article and Find Full Text PDFJ Phys Chem B
October 2015
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Intrinsically disordered protein regions and many other biopolymers lack the three-dimensional structure that could be determined by X-ray crystallography or NMR, which encourages the application of alternative experimental methods. Time-resolved resonance energy transfer data are often used to measure distances between two fluorophores attached to a flexible biopolymer. This is complicated by the rotational and translational diffusion of the fluorophores and by nonmonoexponential donor decay in the absence of the acceptor.
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