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Biology subjects

Tsuchida, M.

Publications and source records attributed to Tsuchida, M..

3 recordsLinked to original sources

Comprehensive molecular profiling of single-cell proteome via gel electrophoresis and 3D single-molecule imaging

Recent advances in shotgun proteomics and immunoassays have yielded powerful single-cell proteomics technologies. However, current methods lack the sensitivity required to comprehensively quantify protein abundances in individual cells. Here, we present single-cell PAGE-PISA, an ultra-sensitive proteome profiling strategy that combines gel electrophoresis with 3D single-molecule fluorescence imaging. Our approach labels all proteins in single cells with fluorescent dyes, separates them by electrophoresis, and counts with single-molecule resolution. This technique quantified over 107 protein copies from a single mammalian cell with the sensitivity to detect low-abundance proteins down to 104 copies per species. Single-cell PAGE-PISA successfully classified cells into distinct cell types based on their proteomic profiles. Furthermore, our single-cell proteome data strongly correlated with predicted developmental states during cardiomyocyte differentiation, providing complementary information to single-cell transcriptome data. Together, single-cell PAGE-PISA enables highly sensitive and quantitative proteome profiling at the single-cell level, capturing subtle proteomic differences that distinguish diverse cellular states.

biophysics↗

The viable but non-culturable (VBNC) state of Campylobacter jejuni lacks propagation ability in the mouse intestinal tract

Campylobacter jejuni is a foodborne pathogen found worldwide. It can exist in a viable but non-culturable (VBNC) state under environmental stresses and cannot be cultured in this state. Whether C. jejuni retains its pathogenicity or causes food poisoning by resuscitation from the VBNC state remains unclear. This research aimed to evaluate whether C. jejuni in the VBNC state should be accounted for in prevention strategies against Campylobacter food poisoning. The VBNC state of C. jejuni strain NCTC11168 was induced at 4{degrees}C under aerobic conditions. A mouse model (C57BL/6, 3-week-old male) was prepared by administering a defined zinc-deficient diet and antibiotics in drinking water. Each mouse was administered C. jejuni with approximately 107 colony-forming units of culturable cells, cells in the VBNC state, or Muller-Hinton broth as a control. In culturable cell-infected mice, an increase in the number of C. jejuni in stool was observed using colony counting and quantitative polymerase chain reaction. No culturable cells were present in VBNC cell-infected mice. Clinical signs, weight loss, or significant increase in lipocalin-2 and myeloperoxidase levels, as inflammatory biomarkers, were not observed in culturable cell- or VBNC cell-infected mice. Thus, culturable cells colonized the mouse intestinal tract, whereas cells in the VBNC state could not. In the VBNC state, C. jejuni may not pose a risk of food poisoning. Further investigations on the colonization and pathogenicity of C. jejuni in the VBNC state in the human intestinal tract are required.

microbiology↗

Modeling cell turning by mechanics at the cell rear

In this study, we explore a simulation of a mechanical model of the keratocyte lamellipodium as previously tested and calibrated for straight steady-state motility [1] and for the process of polarization and motility initiation [2]. In brief, this model uses the balance of three essential forces (myosin contraction, adhesive drag and actin network viscosity) to determine the cells mechanical behavior. Cell shape is set by the balance between the actin polymerization-driven protrusion at the cell boundary and myosin-driven retraction of the actin-myosin network. In the model, myosin acts to generate contractile stress applied to a viscous actin network with viscous resistance to actin flow created by adhesion to the substrate. Previous study [3] demonstrated that similar simple model with uniform constant adhesion predicts a rotating behavior of the cell; however, this behavior is idealized, and does not mimic observed features of the keratocytes turning behavior. Our goal is to explore what are the consequences of introducing mechanosensitive adhesions to the model.

biophysics↗