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Emi Hattori

Bio: Emi Hattori is an academic researcher from University of Tsukuba. The author has contributed to research in topics: Single bond & Viral replication. The author has an hindex of 2, co-authored 3 publications receiving 44 citations.

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Journal ArticleDOI
TL;DR: In this article, the photoexcitation of the first generated open forms gives rise to other open forms which need a double-bond rotation for reversion to the closed form.
Abstract: Picosecond to submillisecond photochromic reactions of 2,4-diphenyl-2H-benzopyran and 2,2,4-triphenyl-2H-benzopyran have been investigated by time-resolved absorption spectroscopy. The C−O bond cleavage of the benzopyrans (closed forms) occurs via the first excited singlet state within 2 ps to produce vibrationally excited open forms in the ground electronic state. In the subnanosecond to submillisecond time domain, several decay components with almost the same spectral profiles are observed. These components are assigned to respective stereoisomers with respect to two double bonds and one single bond of the open enone forms. From the pump-laser power dependencies of the yields of the open forms, it is suggested that the photocleavage gives at first only the open forms revertible to the closed form by a single-bond rotation, and that the photoexcitation of the first generated open forms gives rise to other open forms which need a double-bond rotation for reversion to the closed form. The photochromic reac...

35 citations

Journal ArticleDOI
TL;DR: This study developed a method called “Fate-seq” to comprehensively identify the RNA sequences derived from RNA and DNA viruses, contributing RNA stability in the cells, which have the potential to enhance the stability of viral RNA genomes, thereby augmenting viral replication efficiency and virulence.

13 citations

Journal ArticleDOI
TL;DR: Results suggest that females make a comparative review of courting males before accepting a male and that conspecific song is a factor in criteria affecting female selectivity.
Abstract: Female mate choice plays an important role in sexual isolation. The present study examined sexual isolation using D. simulans and D. mauritiana in conditions where females had no opportunity to compare males versus where females were able to choose males. The sound produced by wing vibration in males (courtship song) affects female receptivity in Drosophila. Females of both species copulated with intact conspecific males more than intact heterospecific males and wingless conspecific and heterospecific males. Drosophila mauritiana females copulated only with intact conspecific males within 30-min observations period without comparing other males, suggesting that absolute criteria are used for decision-making to accept courting males. Females of D. simulans copulated with intact D. mauritiana males as well as wingless D. simulans or D. mauritiana males in no-choice conditions. In a choice situation, D. simulans females copulated with intact D. mauritiana males as well as wingless D. mauritiana males when the females were courted by both types of males, suggesting that D. simulans females accept intact D. mauritiana males as if they are mute. Females of D. simulans copulated with intact D. simulans males as well as intact D. mauritiana males when they were courted by males of either type, whereas they copulated with intact D. simulans males more than intact D. mauritiana males in true choice situations. These results suggest that females make a comparative review of courting males before accepting a male and that conspecific song is a factor in criteria affecting female selectivity.

1 citations


Cited by
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Journal ArticleDOI
TL;DR: The electrophilic cyclization of substituted propargylic aryl ethers by I2, ICl, and PhSeBr produces 3,4-disubstituted 2H-benzopyrans in excellent yields.
Abstract: The electrophilic cyclization of substituted propargylic aryl ethers by I2, ICl, and PhSeBr produces 3,4-disubstituted 2H-benzopyrans in excellent yields. This methodology results in vinylic halides or selenides under mild reaction conditions and tolerates a variety of functional groups, including methoxy, alcohol, aldehyde, and nitro groups.

140 citations

Journal ArticleDOI
TL;DR: In this paper, the authors compared African green monkeys inoculated with infectious SARS-CoV-2 or irradiated, inactivated virus to study the dynamics of virus replication throughout the respiratory tract.
Abstract: Detailed knowledge about the dynamics of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is important for uncovering the viral and host factors that contribute to coronavirus disease 2019 (COVID-19) pathogenesis. Old-World nonhuman primates recapitulate mild to moderate cases of COVID-19, thereby serving as important pathogenesis models. We compared African green monkeys inoculated with infectious SARS-CoV-2 or irradiated, inactivated virus to study the dynamics of virus replication throughout the respiratory tract. Genomic RNA from the animals inoculated with the irradiated virus was found to be highly stable, whereas subgenomic RNA, an indicator of viral replication, was found to degrade quickly. We combined this information with single-cell RNA sequencing of cells isolated from the lung and lung-draining mediastinal lymph nodes and developed new analysis methods for unbiased targeting of important cells in the host response to SARS-CoV-2 infection. Through detection of reads to the viral genome, we were able to determine that replication of the virus in the lungs appeared to occur mainly in pneumocytes, whereas macrophages drove the inflammatory response. Monocyte-derived macrophages recruited to the lungs, rather than tissue-resident alveolar macrophages, were most likely to be responsible for phagocytosis of infected cells and cellular debris early in infection, with their roles switching during clearance of infection. Together, our dataset provides a detailed view of the dynamics of virus replication and host responses over the course of mild COVID-19 and serves as a valuable resource to identify therapeutic targets.

108 citations

Journal ArticleDOI
TL;DR: The exploitation of helicity is demonstrated to develop a novel set of photoresponsive helicenes 2-4 that lead to colored intermediates exhibiting graded stability, and it is shown that the photochromism of 2- 4 in conjunction with response of 2Q-4Q to external stimuli permits development of molecular logic gates with INHIBIT function.
Abstract: Photolysis of regioisomeric helical chromenes 1 and 2 leads to colored reactive intermediates. While the latter generally decay quite rapidly, they are found to be longer lived in 1 and highly persistent in 2. The remarkable stability of the otherwise fleeting transient in 2 allowed isolation and structural characterization by X-ray crystallography. The structural analyses revealed that steric force inherent to the helical scaffold is the origin of stability as well as differentiation in the persistence of the intermediates of 1 and 2 (1Q and 2Q). The structure further shows that diphenylvinyl moiety in the TT isomer of 2Q gets splayed over the helical scaffold such that it is fraught with a huge steric strain to undergo required bond rotations to regenerate the precursor chromene. Otherwise, reversion of 2Q was found to occur at higher temperatures. Aazahelical chromenes 3 and 4 with varying magnitudes of helicity were designed in pursuit of o-quinonoid intermediates with graded activation barriers. Thei...

66 citations

Journal ArticleDOI
TL;DR: The results obtained in the nanosecond time domain show that the triplet marginally participates in the photoreaction for only one of the studied compounds (2,2-spiro-adamantyl-7,8-benzo(2H)chromene), in agreement with the model previously proposed to explain the wavelength dependence of the reaction and emission quantum yields in photostationary experiments.
Abstract: In this paper, the photodynamics of three chromenes (2,2-spiro-adamantyl-7,8-benzo(2H)chromene, 2,2-diphenyl(2H)chromene and 2,2-diphenyl-5,6-benzo(2H)chromene) has been investigated by nano- and femtosecond time resolved techniques in hydrocarbon solutions at room temperature. Using pump–probe techniques, ultrafast steps of molecular dynamics characterizing the photoresponse of chromenes have been investigated: the breakage of the C–O bond was found to occur within a few hundred femtoseconds producing a short-lived transient that converts to the cisoid-cis open form in less than one picosecond and then to the metastable transoid-cis structure within a few picoseconds. The effect of different excitation wavelengths on the formation rate of the first shortest-lived transient of 5,6DPBC is in agreement with the model previously proposed to explain the wavelength dependence of the reaction and emission quantum yields in photostationary experiments. The results obtained in the nanosecond time domain show that the triplet marginally participates in the photoreaction for only one of the studied compounds (2,2-spiro-adamantyl-7,8-benzo(2H)chromene).

55 citations

Journal ArticleDOI
TL;DR: Diarylbenzo-and naphthopyrans are one of the important and well-known classses of organic photochromic systems as discussed by the authors, and their photolysis leads to highly colored o -quinonoid intermediates.
Abstract: Diarylbenzo- and naphthopyrans are one of the important and well-known classses of organic photochromic systems. Their photolysis leads to highly colored o -quinonoid intermediates. The mechanistic details and spectrokinectic properties of the photogenerated colored intermediates have been extensively studied. Accordingly, stereoelectronic effects have been shown to play a crucial role in controlling properties such as spectrokinetics, fatigue resistance and colorability. Much research continues unabated to develop photochromic materials with properties that surpass the existing ones for application in ophthalmic lenses as well as optical data storage devices. In the realm of materials chemistry, the diarylpyran unit is presently exploited as an essential design element to produce functional materials. Given the facile synthetic access to molecular systems that respond to light as an external stimulus leading to widely distinct physicochemical properties, we believe that more exciting research based on diarylpyran photochemistry will germinate in materials chemistry and biology in the near future. This review with a coverage of the phenomenon since its inception to the present state of application for functional materials–through synthesis and mechanistic details–should serve as an invaluable resource to an uninhibited chemist to exploit the photochromism of diarylpyrans for diverse functions/applications.

53 citations