is a convenient host for the expression of proteins, but the heterologous production of large membrane protein complexes often is hampered by the lack of specific accessory genes required for membrane insertion or cofactor assembly. In this study we introduce the non-pathogenic and fast-growing as a suitable expression host for membrane-bound proteins from . We achieved production of the primary Na pump, the NADH:quinone oxidoreductase (NQR), from in an active state, as indicated by increased overall NADH:quinone oxidoreduction activity of membranes from the transformed , and the sensitivity toward Ag, a specific inhibitor of the NQR. Complete assembly of NQR expressed in was demonstrated by BN PAGE followed by activity staining. The secondary transport system Mrp from , another membrane-bound multisubunit complex, was also produced in in a functional state, as demonstrated by Li transport. is a promising expression host for the production of membrane protein complexes from Gram-negative pathogens.
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http://dx.doi.org/10.3389/fmicb.2018.02537 | DOI Listing |
Oncotarget
January 2025
Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Recently, combination checkpoint therapy of cancer has been recognized as producing additive as opposed to synergistic benefit due in part to positively correlated effects. The potential for uncorrelated or negatively correlated therapies to produce true synergistic benefits has been noted. Whereas the inhibitory receptors PD-1, CTLA-4, TIM-3, LAG-3, and TIGIT have been collectively characterized as exhaustion receptors, another inhibitory receptor KLRG1 was historically characterized as a senescent receptor and received relatively little attention as a potential checkpoint inhibitor target.
View Article and Find Full Text PDFJ Infect Dev Ctries
December 2024
Department of Immunology, School of Medicine and Dr. Jose Eleuterio Gonzalez University Hospital, Universidad Autónoma de Nuevo León, Monterrey, Mexico.
Co-inhibitory molecules, such as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and programmed cell death protein 1 (PD-1), known as immune checkpoints, regulate the activity of T and myeloid cells during chronic viral infections and are well-established for their roles in cancer therapy. However, their involvement in chronic bacterial infections, particularly those caused by pathogens endemic to developing countries, such as Mycobacterium tuberculosis (Mtb), remains incompletely understood. Cytokine microenvironment determines the expression of co-inhibitory molecules in tuberculosis: Results indicate that the cytokine IL-12, in the presence of Mtb antigens, can enhance the expression of co-inhibitory molecules while preserving the effector and memory phenotypes of CD4+ T cells.
View Article and Find Full Text PDFNeoplasma
December 2024
Department of Breast Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Triple-negative breast cancer (TNBC) is a highly aggressive subtype of breast malignancy. Although some patients benefit from immune checkpoint therapy, current treatment methods rely mainly on chemotherapy. It is imperative to develop predictors of efficacy and identify individuals who will be sensitive to particular treatment regimens.
View Article and Find Full Text PDFRegarding flotillin knockdown, drug resistance is reversed in colorectal cancer (CRC) cell lines; this is associated with the phosphoinositide 3-kinase/protein kinase B (PI3K/AKT) pathway, as our previous experimental results indicated. However, the exact mechanism underlying this pathway remains unclear. PI3K inhibitor and activator were added separately to clarify the role of the PI3K pathway in reversing drug resistance.
View Article and Find Full Text PDFInvertebr Syst
January 2025
Instituto de Biología, UNAM, Departamento de Zoología, Colección Nacional de Insectos, Apartado Postal 70-153, 04510, Ciudad de México, Mexico.
The superfamily Mantispoidea (Insecta: Neuroptera) includes the families Berothidae, Rhachiberothidae and Mantispidae. Among these taxa, the last two are collectively known as Raptorial Mantispoidea due to the presence of grasping forelegs for predatory habits. The Mantispidae classically included the subfamilies Symphrasinae, Drepanicinae, Calomantispinae and Mantispinae, yet recent research challenged this classification scheme as well as the monophyly of this family resulting in Symphrasinae being transferred to Rhachiberothidae.
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