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Journal articles on the topic 'C-trimer (CT)'

Author: Grafiati

Published: 11 March 2023

Last updated: 31 July 2025

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1

Summer, Dominik, Christine Rangger, Maximilian Klingler, et al. "Exploiting the Concept of Multivalency with 68Ga- and 89Zr-Labelled Fusarinine C-Minigastrin Bioconjugates for Targeting CCK2R Expression." Contrast Media & Molecular Imaging 2018 (2018): 1–12. http://dx.doi.org/10.1155/2018/3171794.

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Cholecystokinin-2 receptors (CCK2R) are overexpressed in a variety of malignant diseases and therefore have gained certain attention for peptide receptor radionuclide imaging. Among extensive approaches to improve pharmacokinetics and metabolic stability of minigastrin (MG) based radioligands, the concept of multivalency for enhanced tumour targeting has not been investigated extensively. We therefore utilized fusarinine C (FSC) as chelating scaffold for novel mono-, di-, and trimeric bioconjugates for targeting CCK2R expression. FSC-based imaging probes were radiolabelled with positron emitti

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2

Jarret, R. L., L. C. Merrick, T. Holms, J. Evans, and M. K. Aradhya. "Simple sequence repeats in watermelon (Citrullus lanatus (Thunb.) Matsum. &Nakai)." Genome 40, no. 4 (1997): 433–41. http://dx.doi.org/10.1139/g97-058.

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Simple sequence repeat length polymorphisms were utilized to examine genetic relatedness among accessions of watermelon (Citrullus lanatus (Thunb.) Matsum. &Nakai). A size-fractionated TaqI genomic library was screened for the occurrence of dimer and trimer simple sequence repeats (SSRs). A total of 96 (0.53%) SSR-bearing clones were identified and the inserts from 50 of these were sequenced. The dinucleotide repeats (CT)n and (GA)n accounted for 82% of the SSRs sequenced. PCR primer pairs flanking seven SSR loci were used to amplify SSRs from 32 morphologically variable watermelon genotyp

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3

Denomme, G. A. "An Adenine Trimer Precedes a C/G Polymorphism in the 3′-Amplimer Region of the Human Platelet Glycoprotein IIIa Intron 6 CT Repeat." Human Heredity 48, no. 2 (1998): 115–18. http://dx.doi.org/10.1159/000022790.

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4

Yartsev, V. M. "Complex conductivity of trimerized quasi-one-dimensional CT crystals: Arbitrary trimer." Synthetic Metals 35, no. 1-2 (1990): 29–38. http://dx.doi.org/10.1016/0379-6779(90)90021-c.

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5

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

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(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail

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6

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

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(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail

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7

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

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(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail

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8

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

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Abstract:

(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail

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9

Chan, Yee-Peng, Min Lu, Somnath Dutta, et al. "Biochemical, Conformational, and Immunogenic Analysis of Soluble Trimeric Forms of Henipavirus Fusion Glycoproteins." Journal of Virology 86, no. 21 (2012): 11457–71. https://doi.org/10.5281/zenodo.13477310.

Full text

Abstract:

(Uploaded by Plazi for the Bat Literature Project) ABSTRACT The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxoviruses discovered in the mid- to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect cells by a pH-independent membrane fusion mechanism facilitated by their attachment (G) and fusion (F) glycoproteins. Here, several soluble forms of henipavirus F (sF) were engineered and characterized. Recombinant sF was produced by deleting the transmembrane (TM) and cytoplasmic tail

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10

Ma, Gary S., Nicolas Aznar, Nicholas Kalogriopoulos, et al. "Therapeutic effects of cell-permeant peptides that activate G proteins downstream of growth factors." Proceedings of the National Academy of Sciences 112, no. 20 (2015): E2602—E2610. http://dx.doi.org/10.1073/pnas.1505543112.

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In eukaryotes, receptor tyrosine kinases (RTKs) and trimeric G proteins are two major signaling hubs. Signal transduction via trimeric G proteins has long been believed to be triggered exclusively by G protein-coupled receptors (GPCRs). This paradigm has recently been challenged by several studies on a multimodular signal transducer, Gα-Interacting Vesicle associated protein (GIV/Girdin). We recently demonstrated that GIV’s C terminus (CT) serves as a platform for dynamic association of ligand-activated RTKs with Gαi, and for noncanonical transactivation of G proteins. However, exogenous manip

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11

Elalouf, Amir, Hanan Maoz, and Amit Yaniv Rosenfeld. "Comprehensive Insights into the Molecular Basis of HIV Glycoproteins." Applied Sciences 14, no. 18 (2024): 8271. http://dx.doi.org/10.3390/app14188271.

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Human Immunodeficiency Virus (HIV) is a diploid, C-type enveloped retrovirus belonging to the Lentivirus genus, characterized by two positive-sense single-stranded RNA genomes, that transitioned from non-human primates to humans and has become globally widespread. In its advanced stages, HIV leads to Acquired Immune Deficiency Syndrome (AIDS), which severely weakens the immune system by depleting CD4+ helper T cells. Without treatment, HIV progressively impairs immune function, making the body susceptible to various opportunistic infections and complications, including cardiovascular, respirat

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12

Vasselli, James Robert, Sophia Frentzas, Andrew James Weickhardt та ін. "Trial in progress: A phase 1-2, first-in-human, open label, dose escalation and expansion study of AU-007, a monoclonal antibody that binds to IL-2 and inhibits IL-2Rα binding, in patients with advanced solid tumors." Journal of Clinical Oncology 40, № 16_suppl (2022): TPS2671. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.tps2671.

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TPS2671 Background: AU-007 is a computationally designed, monoclonal antibody that binds to IL-2 on its CD25 binding epitope. AU-007 bound IL-2 (A/IL-2) cannot bind to high affinity trimeric IL-2 receptors (IL-2R) consisting of CD25, CD122, and CD132 expressed on Tregs and vascular endothelium, but its binding to low affinity dimeric IL-2Rs (CD122 and CD132) expressed on T effector and NK cells is unhindered. Thus, AU-007 redirects endogenously produced or exogenous IL-2 (aldesleukin) towards activation of immune stimulating T effector and NK cells, while diminishing Treg activation and expans

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13

Ljubimov, Alexander V., Rameshwar Patil, Hui Ding, et al. "Abstract 575: Brain delivery of clinically suitable nanobioconjugates to inhibit glioblastoma growth through extracellular matrix-immune cell crosstalk." Cancer Research 83, no. 7_Supplement (2023): 575. http://dx.doi.org/10.1158/1538-7445.am2023-575.

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Abstract Introduction: Tumor growth, invasion, and escape from immune surveillance largely depend on cancer microenvironment. Laminins are trimeric proteins and essential components of glioblastoma (GBM) microenvironment/extracellular matrix (ECM). In brain glioma samples from 230 patients, we found a correlation between the overexpression of tumor ECM protein laminin-411 (α4β1γ1) and faster tumor recurrence with shorter patient survival. Laminin-411 is produced by endothelial cells, neutrophils, monocytes, platelets, lymphocytes, and glioma cells and can modulate the immune system. Novel nano

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14

Alfadhli, Ayna, CeAnn Romanaggi, Robin Lid Barklis, and Eric Barklis. "Second site reversion of HIV-1 envelope protein baseplate mutations maps to the matrix protein." Journal of Virology, January 9, 2024. http://dx.doi.org/10.1128/jvi.01742-23.

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ABSTRACT The HIV-1 Envelope (Env) protein cytoplasmic tail (CT) recently has been shown to assemble an unusual trimeric baseplate structure that locates beneath Env ectodomain trimers. Mutations at linchpin residues that help organize the baseplate impair virus replication in restrictive T cell lines but not in permissive cell lines. We have identified and characterized a second site suppressor of these baseplate mutations, located at residue 34 in the viral matrix (MA) protein, that rescues viral replication in restrictive cells. The suppressor mutation was dependent on the CT to exert its ac

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15

Alfadhli, Ayna, August O. Staubus, Philip R. Tedbury, Mariia Novikova, Eric O. Freed, and Eric Barklis. "Analysis of HIV-1 Matrix-Envelope Cytoplasmic Tail Interactions." Journal of Virology 93, no. 21 (2019). http://dx.doi.org/10.1128/jvi.01079-19.

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ABSTRACT The matrix (MA) domains of HIV-1 precursor Gag (PrGag) proteins direct PrGag proteins to plasma membrane (PM) assembly sites where envelope (Env) protein trimers are incorporated into virus particles. MA targeting to PM sites is facilitated by its binding to phosphatidylinositol-(4,5)-bisphosphate [PI(4,5)P2], and MA binding to cellular RNAs appears to serve a chaperone function that prevents MA from associating with intracellular membranes prior to arrival at the PI(4,5)P2-rich PM. Investigations have shown genetic evidence of an interaction between MA and the cytoplasmic tails (CTs)

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16

Roach, Crystal M., Edith J. Mayorga, Lance H. Baumgard, Jason W. Ross, and Aileen F. Keating. "Zearalenone exposure differentially affects the ovarian proteome in prepubertal gilts during thermal neutral and heat stress conditions." Journal of Animal Science, April 26, 2024. http://dx.doi.org/10.1093/jas/skae115.

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Abstract Zearalenone (ZEN), a nonsteroidal estrogenic mycotoxin, causes endocrine disruption and porcine reproductive dysfunction. Heat stress (HS) occurs when exogenous and metabolic heat accumulation exceeds heat dissipation. Independently, HS and ZEN both compromise swine reproduction; thus, the hypothesis investigated was two-pronged: that ZEN exposure would alter the ovarian proteome and that these effects would differ in thermal neutral and HS pigs. Pre-pubertal gilts (n = 38) were fed ad libitum and assigned to either thermal neutral (TN: 21.0 ± 0.1°C) or HS (12 h cyclic temperatures of

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17

Prchal, Jan, Jakub Sýs, Petra Junková, Jan Lipov, and Tomáš Ruml. "Interaction Interface of Mason-Pfizer Monkey Virus Matrix and Envelope Proteins." Journal of Virology 94, no. 20 (2020). http://dx.doi.org/10.1128/jvi.01146-20.

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ABSTRACT Retroviral envelope glycoprotein (Env) is essential for the specific recognition of the host cell and the initial phase of infection. As reported for human immunodeficiency virus (HIV), the recruitment of Env into a retroviral membrane envelope is mediated through its interaction with a Gag polyprotein precursor of structural proteins. This interaction, occurring between the matrix domain (MA) of Gag and the cytoplasmic tail (CT) of the transmembrane domain of Env, takes place at the host cell plasma membrane. To determine whether the MA of Mason-Pfizer monkey virus (M-PMV) also inter

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18

Maddox, Adam L., and Deepali Bhandari. "Secondary Structure Analysis of the C‐terminus of Ga‐interacting Vesicle Associated Protein Using Circular Dichroism Spectroscopy." FASEB Journal 31, S1 (2017). http://dx.doi.org/10.1096/fasebj.31.1_supplement.913.11.

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A vast majority of cell signaling is mediated through activation of hetero‐trimeric G proteins. Ga‐Interacting Vesicle associated protein (GIV) is a non‐receptor Guanine nucleotide exchange factor (GEF), which activates Gi family of heterotrimeric G proteins downstream of activated receptor tyrosine kinases (RTKs). GIV's GEF function is mediated by a stretch of highly conserved ~20 residues, which is followed by a putative SH2‐like domain in the C‐terminus of the protein. Previous studies have shown that the C‐terminal 211 amino acids of GIV (referred to as “GIV‐CT” henceforth) are capable of

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19

White, Ellen, Fan Wu, Elena Chertova, et al. "Truncating the gp41 Cytoplasmic Tail of Simian Immunodeficiency Virus Decreases Sensitivity to Neutralizing Antibodies without Increasing the Envelope Content of Virions." Journal of Virology 92, no. 3 (2017). http://dx.doi.org/10.1128/jvi.01688-17.

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ABSTRACTAn incomplete understanding of native human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) envelope glycoproteins (Envs) impedes the development of structural models of Env and vaccine design. This shortcoming is due in part to the low number of Env trimers on virus particles. For SIV, this low expression level can be counteracted by truncating the cytoplasmic tail (CT) of Env. CT truncation has been shown to increase Env incorporation into the virion and is commonly used in vaccine and imaging studies, but its effects on viral antigenicity have not been fully elu

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