Detail of Fig5C_HeLa_WT1

Fluorescence images of mCherry fluorescence in the cytoplasm of WT HeLa cells.
Fluorescence images of mCherry fluorescence in the cytoplasm of WT HeLa cells.
Release, Updated
Image data
File Formats
Data size
46.0 KB

Homo sapiens ( NCBITaxon:9606 )
Cell Line
HeLa cell ( CLO_0003684 )
Protein tags

Molecular Function (MF)
biliverdin reductase ( GO:0004074 )
Biological Process (BP)
Cellular Component (CC)
cytoplasm ( GO:0005737 )
Biological Imaging Method
fluorescence microscopy ( Fbbi:00000246 )
X scale
0.621 micrometer/pixel
Y scale
0.621 micrometer/pixel
Z scale
1 micrometer/slice
T scale
143 sec per time interval

Image Acquisition
Experiment type
Microscope type
Acquisition mode
Contrast method
Microscope model
Detector model
Objective model
Filter set

Summary of Methods
See details in Kobachi K, et. al. (2020) Cell Struct Funct., 45(2):131-141.
Related paper(s)

Kenju Kobachi, Sota Kuno, Shinya Sato, Kenta Sumiyama, Michiyuki Matsuda, Kenta Terai (2020) Biliverdin Reductase-A Deficiency Brighten and Sensitize Biliverdin-binding Chromoproteins., Cell structure and function, Volume 45, Number 2, pp. 131-141

Published in 2020 Aug 21 (Electronic publication in June 25, 2020, midnight )

(Abstract) Tissue absorbance, light scattering, and autofluorescence are significantly lower in the near-infrared (NIR) range than in the visible range. Because of these advantages, NIR fluorescent proteins (FPs) are in high demand for in vivo imaging. Nevertheless, application of NIR FPs such as iRFP is still limited due to their dimness in mammalian cells. In contrast to GFP and its variants, iRFP requires biliverdin (BV) as a chromophore. The dimness of iRFP is at least partly due to rapid reduction of BV by biliverdin reductase-A (BLVRA). Here, we established biliverdin reductase-a knockout (Blvra(-/-)) mice to increase the intracellular BV concentration and, thereby, to enhance iRFP fluorescence intensity. As anticipated, iRFP fluorescence intensity was significantly increased in all examined tissues of Blvra(-/-) mice. Similarly, the genetically encoded calcium indicator NIR-GECO1, which is engineered based on another NIR FP, mIFP, exhibited a marked increase in fluorescence intensity in mouse embryonic fibroblasts derived from Blvra(-/-) mice. We expanded this approach to an NIR light-sensing optogenetic tool, the BphP1-PpsR2 system, which also requires BV as a chromophore. Again, deletion of the Blvra gene markedly enhanced the light response in HeLa cells. These results indicate that the Blvra(-/-) mouse is a versatile tool for the in vivo application of NIR FPs and NIR light-sensing optogenetic tools.Key words: in vivo imaging, near-infrared fluorescent protein, biliverdin, biliverdin reductase, optogenetic tool.
(MeSH Terms)

Kenta Terai , Graduate School of Medicine, Kyoto University , Department of Pathology and Biology of Diseases

OMERO Dataset
OMERO Project