Japan and the World: Japan’s Contemporary Geopolitical Challenges – A Volume in Honor of the Memory and Intellectual Legacy of Asakawa Kan’ichi

Yale CEAS Occasional Publication Series - Volume 2https://elischolar.library.yale.edu/ceas_publication_series/1001/thumbnail.jp

A Novel Method for Screening Monoclonal Antibodies Reacting with Antigenic Determinants on Soluble Antigens; A Reversed Indirect-Enzyme Linked Immunosorbent Assay(RI-ELISA)

A novel screening method was established to select new monoclonal antibodies which react with unknown antigenic determinants on molecules bearing antigen determinants reactive with established monoclonal antibodies. This new method is a sandwich assay termed "reversed indirect-enzyme linked immunosorbent assay" (RI-ELISA). Goat antimouse immunoglobulin antibodies are used as the primary immobilized antibody in this assay. They allow the non-purified monoclonal antibodies contained in hybridoma culture supernatants to bind to the microtest plate for enzyme immunoassay (EIA plate) much more efficiently than in the usual sandwich assay where the non-purified monoclonal antibodies are adsorbed directly to the polystyrene surface. The antigen solution is then reacted with the monoclonal antibodies and thereafter enzyme labeled monoclonal antibody with known specificity is added. Therefore, if the hybridoma culture supernatant contains monoclonal antibodies which were bound to the EIA plate and react with antigenic determinants on the soluble molecules which have antigen determinants recognized by the enzyme labeled antibody, the enzyme labeled antibodies will bind to induce an enzymatic reaction. The most important technical consideration in the RI-ELISA is the inhibition of direct binding of the enzyme labeled monoclonal antibodies to free sites remaining in the immobilized goat anti-mouse immunoglobulins antibodies. This problem could be effectively overcome by using normal mouse serum as blocking substance. These studies indicate that the RI-ELISA may be a useful screening method for selecting new monoclonal antibodies which react with unknown antigenic determinants on soluble molecules

Paramyxovirus Sendai virus-like particle formation by expression of multiple viral proteins and acceleration of its release by C protein

AbstractEnvelope viruses maturate by macromolecule assembly and budding. To investigate these steps, we generated virus-like particles (VLPs) by co-expression of structural proteins of Sendai virus (SeV), a prototype of the family Paramyxoviridae. Simultaneous expression of matrix (M), nucleo- (N), fusion (F), and hemagglutinin-neuraminidase (HN) proteins resulted in the generation of VLPs that had morphology and density similar to those of authentic virus particles, although the efficiency of release from cells was significantly lower than that of the virus. By using this VLP formation as a model of virus budding, roles of individual proteins in budding were investigated. The M protein was a driving force of budding, and the F protein facilitated and the HN protein suppressed VLP release. Either of the glycoproteins, F or HN, as well as the N protein, significantly shifted density of VLPs to that of virus particles, suggesting that viral proteins bring about integrity of VLPs by protein–protein interactions. We further found that co-expression of a nonstructural protein, C, but not V, enhanced VLP release to a level comparable to that of virus particles, demonstrating that the C protein plays a role in virus budding

Ferromagnetism in a Hubbard model for an atomic quantum wire: a realization of flat-band magnetism from even-membered rings

We have examined a Hubbard model on a chain of squares, which was proposed by Yajima et al as a model of an atomic quantum wire As/Si(100), to show that the flat-band ferromagnetism according to a kind of Mielke-Tasaki mechanism should be realized for an appropriate band filling in such a non-frustrated lattice. Reflecting the fact that the flat band is not a bottom one, the ferromagnetism vanishes, rather than intensified, as the Hubbard U is increased. The exact diagonalization method is used to show that the critical value of U is in a realistic range. We also discussed the robustness of the magnetism against the degradation of the flatness of the band.Comment: misleading terms and expressions are corrected, 4 pages, RevTex, 5 figures in Postscript, to be published in Phys. Rev. B (rapid communication

Wide and Deep Exploration of Radio Galaxies with Subaru HSC (WERGS). III. Discovery of a z = 4.72 Radio Galaxy with Lyman Break Technique

We report a discovery of $z = 4.72$ radio galaxy, HSC J083913.17+011308.1, by using the Lyman break technique with the Hyper Suprime-Cam Subaru Strategic Survey (HSC-SSP) catalog for VLA FIRST radio sources. The number of known high-$z$ radio galaxies (HzRGs) at $z > 3$ is quite small to constrain the evolution of HzRGs so far. The deep and wide-area optical survey by HSC-SSP enables us to apply the Lyman break technique to a large search for HzRGs. For an HzRG candidate among pre-selected $r$-band dropouts with a radio detection, a follow-up optical spectroscopy with GMOS/Gemini has been performed. The obtained spectrum presents a clear Ly$\alpha$ emission line redshifted to $z=4.72$. The SED fitting analysis with the rest-frame UV and optical photometries suggests the massive nature of this HzRG with $\log{M_*/M_{\odot}} = 11.4$. The small equivalent width of Ly$\alpha$ and the moderately red UV colors indicate its dusty host galaxy, implying a chemically evolved and dusty system. The radio spectral index does not meet a criterion for an ultra-steep spectrum: $\alpha^{325}_{1400}$ of $-1.1$ and $\alpha^{150}_{1400}$ of $-0.9$, demonstrating that the HSC-SSP survey compensates for a sub-population of HzRGs which are missed in surveys focusing on an ultra-steep spectral index.Comment: 10 pages, 5 figures, accepted for publication in A

Subserosal Inflammatory Pseudotumor Causing Intussusception

We present an adult case of intussusception caused by subserosal inflammatory pseudotumor of the terminal ileum. Enteric intussusception was diagnosed by characteristic Xray finding, so called "beak-like" filling defect in the terminal ileum. An exploratory laparotomy revealed focal subserosal thickening in the terminal ileum, and partial ileocolectomy was performed. Microscopically, we identified a pseudotumor that extended through the muscularis propria into serosa. The pseudotumor was composed of fibrous stroma and chronic inflammatory cells with calcification

A Radio-to-millimeter Census of Star-forming Galaxies in Protocluster 4C~23.56 at z = 2.5 : Global and local gas kinematics

We present a study of the gas kinematics of star-forming galaxies associated with protocluster 4C 23.56 at $z=2.49$ using $0''.4$ resolution CO (4-3) data taken with ALMA. Eleven H$\alpha$ emitters (HAEs) are detected in CO (4-3), including six HAEs that were previously detected in CO (3-2) at a coarser angular resolution. The detections in both CO lines are broadly consistent in the line widths and the redshifts, confirming both detections. With an increase in the number of spectroscopic redshifts, we confirm that the protocluster is composed of two merging groups with a total halo mass of $\log{(M_{\rm cl}/M_{\odot})} =13.4-13.6$, suggesting that the protocluster would evolve into a Virgo-like cluster ($>10^{14} M_{\odot}$). We compare the CO line widths and the CO luminosities with galaxies in other (proto)clusters ($n_{\rm gal}=91$) and general fields ($n_{\rm gal}=80$) from other studies. The 4C23.56 protocluster galaxies have CO line widths and luminosities comparable to other protocluster galaxies on average. On the other hand, the CO line widths are on average broader by $\approx50\%$ compared to field galaxies, while the median CO luminosities are similar. The broader line widths can be attributed to both effects of unresolved gas-rich mergers and/or compact gas distribution, which is supported by our limited but decent angular resolution observations and the size estimate of three galaxies. Based on these results, we argue that gas-rich mergers may play a role in the retention of the specific angular momentum to a value similar to that of field populations during cluster assembly, though we need to verify this with a larger number of samples.Comment: 27 pages, 10 figures, 4 tables, ApJ in pres

Helicobacter pylori Seropositivity and Risk of Lung Cancer

Lung cancer is the leading cause of cancer mortality worldwide. Helicobacter pylori (H. pylori) is a risk factor for distal stomach cancer, and a few small studies have suggested that H. pylori may be a potential risk factor for lung cancer. To test this hypothesis, we conducted a study of 350 lung adenocarcinoma cases, 350 squamous cell carcinoma cases, and 700 controls nested within the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study (ATBC) cohort of male Finnish smokers. Controls were one-to-one matched by age and date of baseline serum draw. Using enzyme-linked immunosorbent assays to detect immunoglobulin G antibodies against H. pylori whole-cell and cytotoxin-associated gene (CagA) antigens, we calculated odds ratios (ORs) and 95% confidence intervals (95% CIs) for associations between H. pylori seropositivity and lung cancer risk using conditional logistic regression. H. pylori seropositivity was detected in 79.7% of cases and 78.5% of controls. After adjusting for pack-years and cigarettes smoked per day, H. pylori seropositivity was not associated with either adenocarcinoma (OR: 1.1, 95% CI: 0.75–1.6) or squamous cell carcinoma (OR: 1.1, 95% CI: 0.77–1.7). Results were similar for CagA-negative and CagA-positive H. pylori seropositivity. Despite earlier small studies suggesting that H. pylori may contribute to lung carcinogenesis, H. pylori seropositivity does not appear to be associated with lung cancer