15 research outputs found
Radically Different Thioredoxin Domain Arrangement of ERp46, an Efficient Disulfide Bond Introducer of the Mammalian PDI Family
SummaryThe mammalian endoplasmic reticulum (ER) contains a diverse oxidative protein folding network in which ERp46, a member of the protein disulfide isomerase (PDI) family, serves as an efficient disulfide bond introducer together with Peroxiredoxin-4 (Prx4). We revealed a radically different molecular architecture of ERp46, in which the N-terminal two thioredoxin (Trx) domains with positively charged patches near their peptide-binding site and the C-terminal Trx are linked by unusually long loops and arranged extendedly, forming an opened V-shape. Whereas PDI catalyzes native disulfide bond formation by the cooperative action of two mutually facing redox-active sites on folding intermediates bound to the central cleft, ERp46 Trx domains are separated, act independently, and engage in rapid but promiscuous disulfide bond formation during early oxidative protein folding. Thus, multiple PDI family members likely contribute to different stages of oxidative folding and work cooperatively to ensure the efficient production of multi-disulfide proteins in the ER
DOCK2 is involved in the host genetics and biology of severe COVID-19
「コロナ制圧タスクフォース」COVID-19疾患感受性遺伝子DOCK2の重症化機序を解明 --アジア最大のバイオレポジトリーでCOVID-19の治療標的を発見--. 京都大学プレスリリース. 2022-08-10.Identifying the host genetic factors underlying severe COVID-19 is an emerging challenge. Here we conducted a genome-wide association study (GWAS) involving 2, 393 cases of COVID-19 in a cohort of Japanese individuals collected during the initial waves of the pandemic, with 3, 289 unaffected controls. We identified a variant on chromosome 5 at 5q35 (rs60200309-A), close to the dedicator of cytokinesis 2 gene (DOCK2), which was associated with severe COVID-19 in patients less than 65 years of age. This risk allele was prevalent in East Asian individuals but rare in Europeans, highlighting the value of genome-wide association studies in non-European populations. RNA-sequencing analysis of 473 bulk peripheral blood samples identified decreased expression of DOCK2 associated with the risk allele in these younger patients. DOCK2 expression was suppressed in patients with severe cases of COVID-19. Single-cell RNA-sequencing analysis (n = 61 individuals) identified cell-type-specific downregulation of DOCK2 and a COVID-19-specific decreasing effect of the risk allele on DOCK2 expression in non-classical monocytes. Immunohistochemistry of lung specimens from patients with severe COVID-19 pneumonia showed suppressed DOCK2 expression. Moreover, inhibition of DOCK2 function with CPYPP increased the severity of pneumonia in a Syrian hamster model of SARS-CoV-2 infection, characterized by weight loss, lung oedema, enhanced viral loads, impaired macrophage recruitment and dysregulated type I interferon responses. We conclude that DOCK2 has an important role in the host immune response to SARS-CoV-2 infection and the development of severe COVID-19, and could be further explored as a potential biomarker and/or therapeutic target
The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force
「コロナ制圧タスクフォース」COVID-19患者由来の血液細胞における遺伝子発現の網羅的解析 --重症度に応じた遺伝子発現の変化には、ヒトゲノム配列の個人差が影響する--. 京都大学プレスリリース. 2022-08-23.Coronavirus disease 2019 (COVID-19) is a recently-emerged infectious disease that has caused millions of deaths, where comprehensive understanding of disease mechanisms is still unestablished. In particular, studies of gene expression dynamics and regulation landscape in COVID-19 infected individuals are limited. Here, we report on a thorough analysis of whole blood RNA-seq data from 465 genotyped samples from the Japan COVID-19 Task Force, including 359 severe and 106 non-severe COVID-19 cases. We discover 1169 putative causal expression quantitative trait loci (eQTLs) including 34 possible colocalizations with biobank fine-mapping results of hematopoietic traits in a Japanese population, 1549 putative causal splice QTLs (sQTLs; e.g. two independent sQTLs at TOR1AIP1), as well as biologically interpretable trans-eQTL examples (e.g., REST and STING1), all fine-mapped at single variant resolution. We perform differential gene expression analysis to elucidate 198 genes with increased expression in severe COVID-19 cases and enriched for innate immune-related functions. Finally, we evaluate the limited but non-zero effect of COVID-19 phenotype on eQTL discovery, and highlight the presence of COVID-19 severity-interaction eQTLs (ieQTLs; e.g., CLEC4C and MYBL2). Our study provides a comprehensive catalog of whole blood regulatory variants in Japanese, as well as a reference for transcriptional landscapes in response to COVID-19 infection
Acceleration of Disulfide-Coupled Protein Folding by Positively Charged Glutathione Derivatives
Gly Scan of Prouroguanylin to Investigate Essential Amino Acid Residues for the Intra-Molecular Chaperone Function
Stem-Forming Regions That Are Essential for the Amyloidogenesis of Prion Proteins
Prion diseases represent fatal neurodegenerative disorders
caused
by the aggregation of prion proteins. With regard to the formation
of the amyloidogenic cross-β-structure, the initial mechanism
in the conversion to a β-structure is critically important.
To explore the core regions forming a stem of the amyloid, we designed
and prepared a series of peptides comprised of two native sequences
linked by a turn-inducing dipeptide moiety and examined their ability
to produce amyloids. A sequence alignment of the peptides bearing
the ability to form amyloid structures revealed that paired strands
consisting of VNITI (residues 180–184) and VTTTT (residues
189–193) are the core regions responsible for initiating the
formation of cross-β-structures and for further ordered aggregation.
In addition, most of the causative mutations responsible for inherited
prion diseases were found to be located in these stem-forming regions
on helix H2 and their counterpart on helix H3. Moreover, the volume
effect of the nonstem domain, which contains ∼200 residues,
was deduced to be a determinant of the nature of the association such
as oligomerization, because the stem-forming domain is only a small
part of a prion protein. Taken together, we conclude that the mechanism
underlying the initial stage of amyloidogenesis is the exposure of
a newly formed intramolecular β-sheet to a solvent through the
partial transition of a native structure from an α-helix to
a β-structure. Our results also demonstrate that prion diseases
caused by major prion proteins except the prions of some fungi such
as yeast are inherent only in mammals, as evidenced by a comparison
of the corresponding sequences to the stem-forming regions among different
animals
Design diversity in artificial passive-active circulatory support systems
We have been developing several variations of circulatory assist systems based on nano or micro engineering technologies. One of the special features of the design of these new styles of circulatory assist devices will be a passive controllability according to the native physiological signal transmission and hemodynamic responses. In this study, we presented the design features and the research diversity for the development of passive-active circulatory support systems, such as artificial myocardial assist devices, circulatory valves, epi-cardial or vascular support systems for mechanical assistance in chronic or congenital heart failure patients. We employed a covalent type shape memory alloy fiber as the actuator for the implantable artificial internal organs for sophisticated ventricular or hemodynamic support devices.2 page(s