scholarly journals Tailored flavoproteins acting as light-driven spin machines pump nuclear hyperpolarization

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Yonghong Ding ◽  
Alexey S. Kiryutin ◽  
Ziyue Zhao ◽  
Qian-Zhao Xu ◽  
Kai-Hong Zhao ◽  
...  

Abstract The solid-state photo-chemically induced dynamic nuclear polarization (photo-CIDNP) effect generates non-Boltzmann nuclear spin magnetization, referred to as hyperpolarization, allowing for high gain of sensitivity in nuclear magnetic resonance (NMR). Well known to occur in photosynthetic reaction centers, the effect was also observed in a light-oxygen-voltage (LOV) domain of the blue-light receptor phototropin, in which the functional cysteine was removed to prevent photo-chemical reactions with the cofactor, a flavin mononucleotide (FMN). Upon illumination, the FMN abstracts an electron from a tryptophan to form a transient spin-correlated radical pair (SCRP) generating the photo-CIDNP effect. Here, we report on designed molecular spin-machines producing nuclear hyperpolarization upon illumination: a LOV domain of aureochrome1a from Phaeodactylum tricornutum, and a LOV domain named 4511 from Methylobacterium radiotolerans (Mr4511) which lacks an otherwise conserved tryptophan in its wild-type form. Insertion of the tryptophan at canonical and novel positions in Mr4511 yields photo-CIDNP effects observed by 15N and 1H liquid-state high-resolution NMR with a characteristic magnetic-field dependence indicating an involvement of anisotropic magnetic interactions and a slow-motion regime in the transient paramagnetic state. The heuristic biomimetic design opens new categories of experiments to analyze and apply the photo-CIDNP effect.

2019 ◽  
Vol 67 (43) ◽  
pp. 12037-12043 ◽  
Author(s):  
Sanghwan Ko ◽  
Bora Hwang ◽  
Jung-Hyun Na ◽  
Jisun Lee ◽  
Sang Taek Jung

2021 ◽  
Author(s):  
Xue Zhang ◽  
Christoph Wolf ◽  
Yu Wang ◽  
Hervé Aubin ◽  
Tobias Bilgeri ◽  
...  

Abstract Electron spin resonance (ESR) spectroscopy is a crucial tool to determine the chemical structure of materials. ESR spectra measured in molecular systems, however, are established on large ensembles of spins and usually require complicated structural analysis. Recently, scanning tunneling microscopy (STM) combined with ESR has been proven as a powerful tool to image and coherently control individual atomic spins on surfaces. Here, we extend this technique to demonstrate ESR on single organic molecules - iron phthalocyanine (FePc) - and investigate the magnetic interactions between a molecular spin and either another molecular or atomic spin. We show that the molecular spin density is not only localized at the central Fe atom, but also distributed to the outer ligands, yielding a strongly anisotropic exchange coupling. Our work opens the door for using molecules in nanoscale ESR studies and promises tuning magnetic interactions between non-localized spins via tailoring ligand field symmetry and strength.


2016 ◽  
Vol 55 (11) ◽  
pp. 5254-5265 ◽  
Author(s):  
Philipp Stock ◽  
Eva Deck ◽  
Silvia Hohnstein ◽  
Jana Korzekwa ◽  
Karsten Meyer ◽  
...  

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