Publications by authors named "N Kitamoto"

Article Synopsis
  • Protein knockdown using the auxin-inducible degron (AID) technology helps study protein functions in live cells by rapidly depleting proteins, allowing for immediate observation of phenotypic changes.
  • The original AID system has issues, including unreliable protein degradation (leaky degradation) and a need for high auxin doses, complicating control over protein expression.
  • The new AID version 2 (AID2) improves upon these problems by using a modified mutant and a lower concentration ligand, resulting in faster and more precise protein degradation across human cells, yeast, and even mice.
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Background: Total hemoglobin (tHb) measurement is indispensable for determining the patient's condition (hemorrhagic vs. ischemic) and need for blood transfusion. Conductivity- and absorbance-based measurement methods are used for blood gas analysis of tHb.

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Background: Noninvasive blood-pressure measurement device and pulse oximeter are important for patient monitoring. When these are placed on the same side, cuff inflation sometimes causes measurement failure by pulse oximeter.

Objective: The present study aimed to compare the pulse oximeter alarm frequency and pulse-wave disappearance duration between noninvasive blood-pressure measurement using the deflation method and that using the linear inflation method.

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Benzyl isothiocyanate (BITC), a dietary isothiocyanate (ITC) derived from cruciferous vegetables, has anticancer properties. It is believed that the ITC moiety (-N═C═S) that reacts predominantly with thiol compounds plays a central role in triggering the activities resulting from these properties. Recent studies have demonstrated that ITCs also covalently modify amino moieties in a protein.

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Serotonin (5-hydroxytryptamine) is a putative substrate for myeloperoxidase, which may convert it into the reactive quinone tryptamine-4,5-dione (TD). In this study, we found that the viability of human SH-SY5Y neuroblastoma cells treated with 25 μM TD was increased to approximately 117%. On the other hand, the cell viability was significantly decreased by exposure to TD (150-200 μM), with an increase in intracellular reactive oxygen species (ROS).

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