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@ARTICLE{Hirata:1047709,
author = {Hirata, Keisuke and Fujimiya, Kana and Ostermann, Andreas
and Schrader, Tobias E. and Hiromoto, Takeshi and Goto,
Masataka and Arimori, Takao and Hirano, Yu and Kusaka,
Katsuhiro and Tamada, Taro and Nakamura, Teruya},
title = {{N}eutron and time-resolved {X}-ray crystallography reveal
the substrate recognition and catalytic mechanism of human
{N}udix hydrolase {MTH}1},
journal = {Proceedings of the National Academy of Sciences of the
United States of America},
volume = {122},
number = {29},
issn = {0027-8424},
address = {Washington, DC},
publisher = {National Acad. of Sciences},
reportid = {FZJ-2025-04475},
pages = {e2510085122},
year = {2025},
abstract = {Human MutT homolog 1 (MTH1/NUDT1), which belongs to the
nucleoside diphosphate-linked moiety X (Nudix) hydrolase
family, hydrolyzes oxidized nucleotides such as 8-oxo-dGTP
and 2-oxo-dATP by its broad substrate specificity. MTH1 also
attracts attention as a target molecule in cancer treatment
and the broad substrate recognition of MTH1 is of biological
and medical interests. Previous studies suggested that MTH1
exhibits the broad substrate recognition by changing the
protonation state of Asp119 and Asp120 with much higher pKa.
However, the recognition mechanism is not fully understood
due to the difficulty of directly observing hydrogen atoms.
In addition, recent time-resolved X-ray study proposed that
the Nudix hydrolases catalyze the reactions through a new
three-metal-ion mechanism rather than the two-metal-ion
mechanism previously suggested. To understand the substrate
recognition and catalytic mechanism of human MTH1, we have
performed neutron and time-resolved X-ray crystallography.
Neutron crystallography has visualized the protonation
states of the active site residues, substrates, and water
molecules which are crucial for the substrate-binding and
catalysis, providing direct experimental evidence that the
change in the protonation state of Asp119 and Asp120 is
essential for the broad substrate recognition of MTH1.
Time-resolved X-ray crystallography has visualized a whole
reaction process catalyzed by MTH1 through three Mn2+ ions.
Combination of neutron and time-resolved X-ray
crystallography has proposed a three-metal-ion mechanism of
MTH1 including nucleophilic substitution by a water molecule
and its possible deprotonation pathway. The three-metal-ion
mechanism would be a general feature in the catalytic
reactions of the Nudix hydrolases.},
cin = {JCNS-FRM-II / MLZ / JCNS-4},
ddc = {500},
cid = {I:(DE-Juel1)JCNS-FRM-II-20110218 / I:(DE-588b)4597118-3 /
I:(DE-Juel1)JCNS-4-20201012},
pnm = {6G4 - Jülich Centre for Neutron Research (JCNS) (FZJ)
(POF4-6G4) / 632 - Materials – Quantum, Complex and
Functional Materials (POF4-632)},
pid = {G:(DE-HGF)POF4-6G4 / G:(DE-HGF)POF4-632},
experiment = {EXP:(DE-MLZ)BIODIFF-20140101},
typ = {PUB:(DE-HGF)16},
doi = {10.1073/pnas.2510085122},
url = {https://juser.fz-juelich.de/record/1047709},
}