Measuring Cosmic Rays with the RadMap Telescope on the International Space Station

The RadMap Telescope is a new radiation-monitoring instrument operating in the U.S. Orbital Segment (USOS) of the International Space Station (ISS). The instrument was commissioned in May 2023 and will rotate through four locations inside American, European, and Japanese modules over a period of about six months. In some locations, it will take data alongside operational, validated detectors for a cross-check of measurements. RadMap’s central detector is a finely segmented tracking calorimeter that records detailed depth-dose data relevant to studies of the radiation exposure of the ISS crew. It is also able to record particle-dependent energy spectra of cosmic-ray nuclei with energies up to several hundred MeV per nucleon. A unique feature of the detector is its ability to track nuclei with omnidirectional sensitivity at an angular resolution of two degrees. In this contribution, we present the design and capabilities of the RadMap Telescope and give an overview of the instrument’s commissioning on the ISS

Geometric and Electronic Structures of the NiI and Methyl−NiIII Intermediates of Methyl-Coenzyme M Reductase†

ABSTRACT: Methyl-coenzyme M reductase (MCR) catalyzes the terminal step in the formation of biological methane from methyl-coenzyme M (Me-SCoM) and coenzyme B (CoBSH). The active site in MCR contains a Ni-F430 cofactor, which can exist in different oxidation states. The catalytic mechanism of methane formation has remained elusive despite intense spectroscopic and theoretical investigations. On the basis of spectroscopic and crystallographic data, the first step of the mechanism is proposed to involve a nucleophilic attack of the NiI active state (MCRred1) on Me-SCoM to form a NiIII-methyl intermediate, while computational studies indicate that the first step involves the attack of NiI on the sulfur of Me-SCoM, forming a CH3 radical and a NiII-thiolate species. In this study, a combination of Ni K-edge X-ray absorption spectroscopic (XAS) studies and density functional theory (DFT) calculations have been performed on the NiI (MCRred1), NiII (MCRred1-silent), and NiIII-methyl (MCRMe) states of MCR to elucidate the geometric and electronic structures of the different redox states. Ni K-edge EXAFS data are used to reveal a five-coordinate active site with an open upper axial coordination site in MCRred1. Ni K-pre-edge and EXAFS data and time-dependent DFT calculations unambiguously demonstrate the presence of a long Ni-C bond (∼2.04 Å) in the NiIII-methyl state of MCR. The formation and stability of this species support mechanism I, and the Ni-C bond length suggests a homolytic cleavage of the NiIII-methyl bon