General · EdgepediaSeptember 21, 20266 min read

Hideaki Kato

Hideaki Kato (加藤英明) is a Japanese structural biologist who works on membrane proteins, including G protein-coupled receptors and channelrhodopsins, and has been professor at the Research Center for Advanced Science and Technology (RCAST), The University of Tokyo, since February 2024.¹ He trained in Osamu Nureki's laboratory at Tokyo and completed a postdoctoral fellowship in Brian Kobilka's laboratory at Stanford before establishing his own group in 2019.² His laboratory combines cryo-electron microscopy, protein engineering, and electrophysiology to determine the structures of light-sensing proteins and to engineer them as optogenetic tools.³


Field	Structural biology of membrane proteins: GPCRs, rhodopsins, channels, and transporters³
Current position	Professor, RCAST, The University of Tokyo, since February 2024¹
Training	Ph.D. 2009–2014, Osamu Nureki lab, The University of Tokyo; postdoc 2014–2019, Brian Kobilka lab, Stanford School of Medicine²
Signature work	2.5–2.7 Å cryo-EM structures of the potassium-selective channelrhodopsins HcKCR1 and HcKCR2, Cell, 2023⁴
Other landmark structures	ChRmine at 2.0 Å (Cell, 2022); neurotensin receptor 1–Gi1 complex (Nature, 2019); channelrhodopsin crystal structure (Nature, 2012)⁵^•⁶^•⁷
Lab methods	Cryo-electron microscopy, artificial intelligence, electrophysiology, molecular pharmacology³
Funding	JST PRESTO researcher, October 2017–March 2021; JSPS Grant-in-Aid for Scientific Research (A), April 2022–March 2027⁶

Education and training

Kato earned his B.S. in Biophysics and Biochemistry at the Faculty of Science of The University of Tokyo from 2005 to 2009, and his Ph.D. in the same department from 2009 to 2014 in Osamu Nureki's laboratory.² His doctoral work produced high-resolution crystal structures of microbial rhodopsins: the 2012 Nature paper reporting the crystal structure of the channelrhodopsin light-gated cation channel (Nature 482, 369–374) and the 2015 Nature paper on the structural basis of Na+ transport by a light-driven sodium pump (Nature 521, 48–53).⁷

According to his researchmap profile, from May 2014 to March 2019 he was a postdoctoral fellow in the Department of Molecular and Cellular Physiology at Stanford University School of Medicine, in Brian Kobilka's laboratory.²^•⁶ The Stanford period produced his 2019 Nature first-author paper, "Conformational transitions of a neurotensin receptor 1–Gi1 complex" (Nature 572, 80–85, August 2019), which reported the conformational states of a GPCR bound to its heterotrimeric G protein.⁶

Career record

Kato established his own laboratory at The University of Tokyo in 2019.⁸ He served as associate professor in the Department of Life Sciences from April 2019 to January 2024, with an adjunct associate professorship in the Graduate School of Science from April 2020 and adjunct professor from February 2024.⁶ He has also held a joint appointment as associate professor in the Department of Biological Sciences, Graduate School of Science, since 2020.⁷ In February 2024 he became professor at RCAST, where he leads the Structural Bioengineering Kato Laboratory; the JSPS KAKEN database records him as professor there in 2026.¹^•⁹

Representative work

His 2023 Cell paper, "Structural basis for ion selectivity in potassium-selective channelrhodopsins", presented 2.5–2.7 Å cryo-electron microscopy structures of HcKCR1 and HcKCR2, potassium-selective channelrhodopsins from Hyphochytrium catenoides, together with a structure-guided mutant with enhanced K+ selectivity.⁴ The structures showed that potassium selectivity is achieved not by the symmetrical selectivity filter of canonical potassium channels but by three extracellular-vestibule residues within each monomer forming a flexible asymmetric selectivity gate, with a distinct dehydration pathway extending intracellularly.⁴ Building on the structures, the paper reported engineered variants KALI-1 and KALI-2 with increased K+ selectivity, which the authors describe as offering advantages for optogenetic inhibition in vitro and in vivo.⁴

Channelrhodopsins and optogenetics

Channelrhodopsins are light-gated ion channels from microbes; because they can be expressed in neurons and controlled by light, their structures guide the engineering of optogenetic tools, proteins that let researchers switch defined cells on or off with illumination, according to the Structural Bioengineering Kato Laboratory at RCAST.³ Kato's 2022 Cell paper presented a 2.0 Å resolution cryo-EM structure of ChRmine, a cation-conducting channelrhodopsin with large photocurrents, a red-shifted spectrum, and extreme light sensitivity, revealing atypical features: trimeric assembly, a short transmembrane helix 3, a twisting extracellular loop 1, large vestibules within the monomer, and an opening at the trimer interface.⁵ According to the RCSB Protein Data Bank, the coordinates are deposited as entry 7W9W at 2.02 Å resolution, from Rhodomonas lens.¹⁰ According to the 2022 Cell study on the structural basis of ChRmine, the team used the structure to design three engineered proteins for neuroscience applications: rsChRmine (further red-shifted), hsChRmine (high-speed), and frChRmine (combining faster and more red-shifted performance).⁵

Several structural questions are contested between groups. A 2023 Nature Communications study independently determined atomic cryo-EM structures of HcKCR1 and the Na+-selective HcCCR in peptidiscs and attributed K+ versus Na+ selectivity to two distinct sites on the ion conduction pathway, an intracellular residue patch (Leu69/Phe69, Ile73/Ser73, and Asp116) and an extracellular aromatic cluster (primarily Trp102 and Tyr222), a mechanistic account that differs from the asymmetric-gate model of the 2023 Cell paper.¹¹ The same study also reports that HcCCR is Na+ selective with a PK/PNa more than 100-fold smaller than HcKCR1, and suggests its smaller relative proton permeability could make it a neuronal-activation tool less likely to acidify the cytoplasm.¹¹ A separate 2022 Nature Communications study solved cryo-EM structures of ChRmine in lipid nanodiscs, revealing a trimeric architecture with a lipid-filled central pore, and identified ChRmine variants with ten-fold decreased and two-fold increased closing rates.¹²

Current work since 2024

At RCAST the laboratory integrates cryo-electron microscopy, artificial intelligence, electrophysiology, and molecular pharmacology, investigating how organisms perceive and respond to light to develop optogenetic tools, and carrying out structural and functional analyses of proteins activated by hormones, neurotransmitters, odorants, pH, pressure, and temperature, such as GPCRs, to identify drug targets.³ The laboratory's stated research areas are structural biology, protein engineering, rhodopsins, GPCRs, optogenetics and magnetogenetics, and its stated subjects include discovery and structural-functional analysis of novel photo- and magnetoreceptor proteins and spatiotemporal analysis of GPCR signaling.³^•¹³ In March 2025 a Nature Communications paper with Kato as last and corresponding author examined pump-like channelrhodopsins.⁶

Honors and funding

Kato was a JST PRESTO researcher from October 2017 to March 2021 and holds a JSPS Grant-in-Aid for Scientific Research (A) running from April 2022 to March 2027.⁶ His KAKEN principal-investigator profile lists GPCR, cryo-electron microscopy, structural biology, rhodopsins, and tool development among his keywords.⁹

References

Topic: Encyclopedia › Life and health › Life and health scientists › Life scientists › Researchers in structural biology, biochemistry, and biophysics › Membrane proteins and ion channels

Initially written Sep 21, 2026 · Reviewed: Sep 25, 2026 · Edited: Sep 25, 2026; Oct 11, 2026 · Last review: Sep 25, 2026

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