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- Research ArticleResearch ArticleOpen Access
The SARS-CoV2 envelope differs from host cells, exposes procoagulant lipids, and is disrupted in vivo by oral rinses
Journal of Lipid ResearchVol. 63Issue 6100208Published online: April 14, 2022- Zack Saud
- Victoria J. Tyrrell
- Andreas Zaragkoulias
- Majd B. Protty
- Evelina Statkute
- Anzelika Rubina
- and others
Cited in Scopus: 9The lipid envelope of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an essential component of the virus; however, its molecular composition is undetermined. Addressing this knowledge gap could support the design of antiviral agents as well as further our understanding of viral-host protein interactions, infectivity, pathogenicity, and innate immune system clearance. Lipidomics revealed that the virus envelope comprised mainly phospholipids (PLs), with some cholesterol and sphingolipids, and with cholesterol/phospholipid ratio similar to lysosomes. - Research ArticleResearch ArticleOpen Access
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
Journal of Lipid ResearchVol. 63Issue 6100209Published online: April 20, 2022- Weilai Dong
- Karen H.Y. Wong
- Youbin Liu
- Michal Levy-Sakin
- Wei-Chien Hung
- Mo Li
- and others
Cited in Scopus: 0Low levels of high density lipoprotein-cholesterol (HDL-C) are associated with an elevated risk of arteriosclerotic coronary heart disease. Heritability of HDL-C levels is high. In this research discovery study, we used whole-exome sequencing to identify damaging gene variants that may play significant roles in determining HDL-C levels. We studied 204 individuals with a mean HDL-C level of 27.8 ± 6.4 mg/dl (range: 4–36 mg/dl). Data were analyzed by statistical gene burden testing and by filtering against candidate gene lists. - Research ArticleResearch ArticleOpen Access
Sulfatide with ceramide composed of phytosphingosine (t18:0) and 2-hydroxy FAs in renal intercalated cells
Journal of Lipid ResearchVol. 63Issue 6100210Published online: April 15, 2022- Keiko Nakashima
- Yukie Hirahara
- Taro Koike
- Susumu Tanaka
- Keizo Gamo
- Souichi Oe
- and others
Cited in Scopus: 2Diverse molecular species of sulfatide with differences in FA lengths, unsaturation degrees, and hydroxylation statuses are expressed in the kidneys. However, the physiological functions of specific sulfatide species in the kidneys are unclear. Here, we evaluated the distribution of specific sulfatide species in the kidneys and their physiological functions. Electron microscopic analysis of kidneys of Cst-deficient mice lacking sulfatide showed vacuolar accumulation in the cytoplasm of intercalated cells in the collecting duct, whereas the proximal and distal tubules were unchanged. - Research ArticleResearch ArticleOpen Access
Genetic dissection in mice reveals a dynamic crosstalk between the delivery pathways of vitamin A
Journal of Lipid ResearchVol. 63Issue 6100215Published online: April 19, 2022- Jean Moon
- Srinivasagan Ramkumar
- Johannes von Lintig
Cited in Scopus: 2Vitamin A is distributed within the body to support chromophore synthesis in the eyes and retinoid signaling in most other tissues. Two pathways exist for the delivery of vitamin A: the extrinsic pathway transports dietary vitamin A in lipoproteins from intestinal enterocytes to tissues, while the intrinsic pathway distributes vitamin A from hepatic stores bound to serum retinol binding protein (RBP). Previously, the intestine-specific homeodomain transcription factor (ISX) and the RBP receptor STRA6 were identified as gatekeepers of these pathways; however, it is not clear how mutations in the corresponding genes affect retinoid homeostasis. - Research ArticleResearch ArticleOpen Access
Sortilin enhances secretion of apolipoprotein(a) through effects on apolipoprotein B secretion and promotes uptake of lipoprotein(a)
Journal of Lipid ResearchVol. 63Issue 6100216Published online: April 22, 2022- Justin R. Clark
- Matthew Gemin
- Amer Youssef
- Santica M. Marcovina
- Annik Prat
- Nabil G. Seidah
- and others
Cited in Scopus: 2Elevated plasma lipoprotein(a) (Lp(a)) is an independent, causal risk factor for atherosclerotic cardiovascular disease and calcific aortic valve stenosis. Lp(a) is formed in or on hepatocytes from successive noncovalent and covalent interactions between apo(a) and apoB, although the subcellular location of these interactions and the nature of the apoB-containing particle involved remain unclear. Sortilin, encoded by the SORT1 gene, modulates apoB secretion and LDL clearance. We used a HepG2 cell model to study the secretion kinetics of apo(a) and apoB. - Research ArticleResearchOpen Access
Proteomic Analysis Uncovers Measles Virus Protein C Interaction With p65–iASPP Protein Complex
Molecular & Cellular ProteomicsVol. 20100049Published online: January 27, 2021- Alice Meignié
- Chantal Combredet
- Marc Santolini
- István A. Kovács
- Thibaut Douché
- Quentin Giai Gianetto
- and others
Cited in Scopus: 0In Brief Control of measles virus infection and measles-based oncolytic therapy are possible, thanks to the existence of a safe and efficient live attenuated vaccine. Molecular mechanisms that make this vaccine to be so efficient are yet to be determined. We show that the measles C protein is responsible for the establishment of complex networks of interactions with the host cell. We suggest that the C protein binding to the p65–iASPP protein complex controls the host cell death and innate immunity pathways. - Research ArticleResearchOpen Access
Dynamic Changes to the Skeletal Muscle Proteome and Ubiquitinome Induced by the E3 Ligase, ASB2β
Molecular & Cellular ProteomicsVol. 20100050Published online: January 28, 2021- Craig A. Goodman
- Jonathan R. Davey
- Adam Hagg
- Benjamin L. Parker
- Paul Gregorevic
Cited in Scopus: 9In Brief The E3 ubiquitin ligase ASB2β has been identified as a regulator of skeletal muscle mass. To gain insights into potential mechanisms of action, mouse muscles expressing a Flag-tagged ASB2β were investigated using quantitative proteomic methods. The results identified ASB2β-induced changes in the abundance and ubiquitination of proteins associated with mitochondria, the sarcomere, and the cytoskeleton. Additional in vitro studies identified novel putative ASB2β target substrates. The results highlight the complex relationship between protein abundance and ubiquitination in ASB2β-mediated muscle adaptation. - Research ArticleResearchOpen Access
New Proteomic Signatures to Distinguish Between Zika and Dengue Infections
Molecular & Cellular ProteomicsVol. 20100052Published online: February 11, 2021- Kristina Allgoewer
- Shuvadeep Maity
- Alice Zhao
- Lauren Lashua
- Moti Ramgopal
- Beni N. Balkaran
- and others
Cited in Scopus: 0In Brief Differentiation between the mosquito-borne Zika and dengue Flavivirus infections is clinically important for correct treatment, but remains challenging. We used mass spectrometry to quantify expression levels for 277 proteins measured in serum samples from 62 patients, providing a resource to the community. We identified 13 proteins with significant differential expression between the closely related types of infections. Most of the proteins link to pregnancy and brain function. We also identified expression signatures that mark ambiguous infections with respect to temporal differences. - Research ArticleResearchOpen Access
Protein Phosphorylation in Depolarized Synaptosomes: Dissecting Primary Effects of Calcium from Synaptic Vesicle Cycling
Molecular & Cellular ProteomicsVol. 20100061Published online: February 11, 2021- Ivan Silbern
- Kuan-Ting Pan
- Maksims Fiosins
- Stefan Bonn
- Silvio O. Rizzoli
- Eugenio F. Fornasiero
- and others
Cited in Scopus: 0In Brief Analysis of protein phosphorylation in isolated nerve terminals (synaptosomes) treated with C. botulinum neurotoxins (BoNT) to inhibit synaptic vesicle (SV) cycling reveals phosphorylation events that are primarily dependent on depolarization-induced Ca2+ influx and those that also require active SV-cycling machinery. In particular, SV-cycling-dependent phosphorylation sites on synaptobrevin (Vamp2), syntaxin-1 (Stx1a), and cannabinoid receptor-1 (Cnr1) are capable of changing the rate of exo- and endocytosis in cultured hippocampal neurons. - Research ArticleResearchOpen Access
Quantitative Proteomics and Phosphoproteomics Support a Role for Mut9-Like Kinases in Multiple Metabolic and Signaling Pathways in Arabidopsis
Molecular & Cellular ProteomicsVol. 20100063Published online: March 4, 2021- Margaret E. Wilson
- Shin-Cheng Tzeng
- Megan M. Augustin
- Matthew Meyer
- Xiaoyue Jiang
- Jae H. Choi
- and others
Cited in Scopus: 0In Brief The MUT9-like kinases are a family of plant-specific nuclear-localized kinases with roles in diverse signaling pathways, including light sensing, phytohormone perception, and the circadian clock. The proteome and phosphoproteome of compound mlk mutant seedlings have been determined under light and dark conditions. These experiments identify new roles for these kinases regulating secondary plant metabolism and stress responses, tested through metabolite analysis and assaying seedling sensitivity to DNA damaging agents. - Research ArticleResearchOpen Access
Proximity-dependent Mapping of the Androgen Receptor Identifies Kruppel-like Factor 4 as a Functional Partner
Molecular & Cellular ProteomicsVol. 20100064Published online: February 25, 2021- Lauriane Vélot
- Frédéric Lessard
- Félix-Antoine Bérubé-Simard
- Christophe Tav
- Bertrand Neveu
- Valentine Teyssier
- and others
Cited in Scopus: 0In Brief A proximity interaction network for the androgen receptor (AR) was obtained from androgen-responsive prostate cancer cells. A total of 267 candidates were identified, most associating following ligand stimulation, including Krüppel-like factor 4 (KLF4). KLF4 and AR were found to colocalize genome-wide on 4097 genes including PSA (KLK3), for which KLF4 acts as a repressor, without regulating the expression of AR. These results are instrumental to further dissect the molecular mechanisms underlying androgen signaling in prostate cells. - Technological Innovation and ResourcesTechnological Innovation and ResourcesOpen Access
Stable Isotope Labeling of Amino Acids in Flies (SILAF) Reveals Differential Phosphorylation of Mitochondrial Proteins Upon Loss of OXPHOS Subunits
Molecular & Cellular ProteomicsVol. 20100065Published online: February 25, 2021- Florian A. Rosenberger
- Ilian Atanassov
- David Moore
- Javier Calvo-Garrido
- Marco F. Moedas
- Anna Wedell
- and others
Cited in Scopus: 0In Brief We advanced a fully composed food source for Drosophila melanogaster into a highly efficient, versatile, and cheap labeling method, termed SILAF. The larval proteome incorporates more than 99% heavy lysine-6 label within 6 days, while the adult fly metabolism allows protein turnover studies. We obtained a phosphoproteome with site-specific occupancy in a fly model of mitochondrial metabolic disease, highlighting the regulation of two novel conserved phosphosites on subunits of the electron transport chain. - Research ArticleResearchOpen Access
Secretome and Comparative Proteomics of Yersinia pestis Identify Two Novel E3 Ubiquitin Ligases That Contribute to Plague Virulence
Molecular & Cellular ProteomicsVol. 20100066Published online: February 21, 2021- Shiyang Cao
- Yuling Chen
- Yanfeng Yan
- Songbiao Zhu
- Yafang Tan
- Tong Wang
- and others
Cited in Scopus: 2In Brief Rapid adaption to the environments is critical for microbes to establish infection. Quantitative proteome and secretome analyses of Y. pestis grown under conditions mimicking its two typical natural niches were performed to understand the adaption strategies of this deadly pathogen. We identified three secreted proteins that can be translocated into host cells and further demonstrated that two of them show strong E3 ubiquitin ligase activity and contribute significantly to the virulence of Y. pestis. - Research ArticleResearchOpen Access
Proteomic Profiling of Gastric Signet Ring Cell Carcinoma Tissues Reveals Characteristic Changes of the Complement Cascade Pathway
Molecular & Cellular ProteomicsVol. 20100068Published online: March 3, 2021- Yang Fan
- Bin Bai
- Yuting Liang
- Yan Ren
- Yanxia Liu
- Fenli Zhou
- and others
Cited in Scopus: 0In Brief This study took advantages of LCM and DIA-MS, generating a data set in the context of different subtypes of gastric tumors, globally and precisely. It was discovered for the first time that the complement cascade in SRCC tumors was specifically activated compared with AC. - Research ArticleResearch Special Issue: GlycoproteomicsOpen Access
Quantitative Proteomics Reveals that the OGT Interactome Is Remodeled in Response to Oxidative Stress
Molecular & Cellular ProteomicsVol. 20100069Published online: March 11, 2021- Marissa Martinez
- Santosh Renuse
- Simion Kreimer
- Robert O’Meally
- Peter Natov
- Anil K. Madugundu
- and others
Cited in Scopus: 0In Brief The goal of these studies was to provide insight into the regulation of the O-GlcNAc transferase (OGT) basally and in response to oxidative stress, as well as the role that O-GlcNAc plays in promoting cytoprotection. Using quantitative proteomics, the basal and injury-induced interactome of OGT has been defined and validated. Protein interactors are anticipated to regulate either the activity or substrate targeting of OGT, or to be substrates of OGT, thus affecting cytoprotection. - Research ArticleResearchOpen Access
Integrative Proteomic and Metabolomic Analysis Reveals Metabolic Phenotype in Mice With Cardiac-Specific Deletion of Natriuretic Peptide Receptor A
Molecular & Cellular ProteomicsVol. 20100072Published online: March 30, 2021- Pan Chang
- Yan Niu
- Xiaomeng Zhang
- Jing Zhang
- Xihui Wang
- Xi Shen
- and others
Cited in Scopus: 0In Brief Metabolomic analysis in mice revealed that natriuretic peptide receptor A (NPRA) is mainly involved in nucleotide biosynthesis and histidine metabolism in cardiac tissues, and in creatine metabolism, TCA cycle and pentose phosphate pathway in the plasma. Furthermore, proteomics revealed that Cox7c, Cox7b, ATP5J2, Uqcr10, and Myh7 play a vital role in the regulation of metabolic pathway. Together, deterioration of NPRA results in metabolic dysfunction involved with a protein and metabolite-interacting pathway. - Research ArticleResearchOpen Access
Integrated Redox Proteomic Analysis Highlights New Mechanisms of Sensitivity to Silver Nanoparticles
Molecular & Cellular ProteomicsVol. 20100073Published online: March 20, 2021- Reetta Holmila
- Hanzhi Wu
- Jingyun Lee
- Allen W. Tsang
- Ravi Singh
- Cristina M. Furdui
Cited in Scopus: 0In Brief Silver nanoparticles (AgNPs) are widely used nanomaterials, but the molecular mechanisms underlying their activity remain elusive. Here, we show using time course studies that AgNP-sensitive lung cells experience broader and more pronounced changes in protein abundance and protein oxidation impacting protein translation and modification, lipid metabolism, bioenergetics, and mitochondrial dynamics. The findings are further validated by imaging of mitochondria using confocal microscopy and transmission electron microscopy. - Research ArticleResearch Special Issue: GlycoproteomicsOpen Access
Domain Mapping of Chondroitin/Dermatan Sulfate Glycosaminoglycans Enables Structural Characterization of Proteoglycans
Molecular & Cellular ProteomicsVol. 20100074Published online: March 20, 2021- Andrea Persson
- Mahnaz Nikpour
- Egor Vorontsov
- Jonas Nilsson
- Göran Larson
Cited in Scopus: 0In Brief Glycosaminoglycans (GAGs) remain one of the most challenging posttranslational modifications to study, much due to their structural complexity and heterogeneity, and new methods for analysis are therefore required. We have developed a protocol for enrichment and structural characterization of GAGs of proteoglycans using nLC-MS/MS. We provide detailed information on the nonreducing end, internal, and linkage region GAG domains and use the data to determine an overall GAG structure of chromogranin-A of rat INS-1832/13 cells. - Research ArticleResearchOpen Access
Mapping Isoform Abundance and Interactome of the Endogenous TMPRSS2-ERG Fusion Protein by Orthogonal Immunoprecipitation–Mass Spectrometry Assays
Molecular & Cellular ProteomicsVol. 20100075Published online: March 22, 2021- Zhiqiang Fu
- Yasmine Rais
- Tarek A. Bismar
- M. Eric Hyndman
- X. Chris Le
- Andrei P. Drabovich
Cited in Scopus: 0In Brief Orthogonal immunoprecipitation-mass spectrometry assays quantified TMPRSS2-ERG fusion protein (∼27,000 copies/cell) and its four distinct isoforms, and revealed that T1E4-ERG isoform accounted for 52 ± 3% of the total ERG in VCaP cells and 50 ± 11% in FFPE prostate cancer tissues. Methionine-truncated and N-acetylated peptide TASSSSDYGQTSK unique for T1/E4 TMPRSS2-ERG fusion was identified. Unlike the N-terminal antibodies, C-terminal antibodies identified 29 ERG-interacting proteins, including mutually exclusive BRG1- and BRM-associated canonical SWI/SNF chromatin remodeling complexes. Clinical perspectives of assays were discussed. - Research ArticleResearch Special Issue: GlycoproteomicsOpen Access
In-depth Site-specific Analysis of N-glycoproteome in Human Cerebrospinal Fluid and Glycosylation Landscape Changes in Alzheimer's Disease
Molecular & Cellular ProteomicsVol. 20100081Published online: April 13, 2021- Zhengwei Chen
- Qinying Yu
- Qing Yu
- Jillian Johnson
- Richard Shipman
- Xiaofang Zhong
- and others
Cited in Scopus: 0In Brief An exploratory glycosylation-based biomarker study has been conducted for in-depth mapping of an overall glycosylation landscape and site-specific alteration in glycoproteome collected from cerebrospinal fluids (CSF) in healthy control and Alzheimer’s disease (AD) subjects. The comparison will shed light on the glycoproteome profile, dominant glycosylation differences and similarities, and some of the interesting glycoprotein candidates with specific glycosylation pattern alterations in AD. - Research ArticleResearchOpen Access
Feature Selection Methods for Protein Biomarker Discovery from Proteomics or Multiomics Data
Molecular & Cellular ProteomicsVol. 20100083Published online: April 19, 2021- Zhiao Shi
- Bo Wen
- Qiang Gao
- Bing Zhang
Cited in Scopus: 0In Brief Untargeted mass spectrometry–based proteomics provides a powerful platform for protein biomarker discovery, but clinical translation depends on the selection of a small number of proteins for verification and validation. We present feature selection methods for protein biomarker selection from proteomics or multiomics data. The algorithms show good performance, enable functional interpretation of the identified markers, and provide alternative choices for each identified marker to facilitate a robust transition to the verification and validation platforms. - Technological Innovation and ResourcesTechnological Innovation and ResourcesOpen Access
Enabling Photoactivated Cross-Linking Mass Spectrometric Analysis of Protein Complexes by Novel MS-Cleavable Cross-Linkers
Molecular & Cellular ProteomicsVol. 20100084Published online: April 26, 2021- Craig Gutierrez
- Leah J. Salituro
- Clinton Yu
- Xiaorong Wang
- Sadie F. DePeter
- Scott D. Rychnovsky
- and others
Cited in Scopus: 0In Brief Although photochemistry complements residue-specific chemistry through labeling amino acids nonspecifically, existing photo-cross-linking reagents are thus far inapplicable to multisubunit protein complexes owing to low yields and high complexities of photo-cross-linked products. The development of the three sulfoxide-containing MS-cleavable photoreactive SDASO cross-linkers permits MSn-based analytical workflow for accurate identification of photo-cross-linked peptides, enabling complex PPI profiling for the first time. This work has established a solid foundation for future applications of photo-cross-linking in complex XL-MS studies. - Research ArticleResearchOpen Access
Calculating Sample Size Requirements for Temporal Dynamics in Single-Cell Proteomics
Molecular & Cellular ProteomicsVol. 20100085Published online: April 26, 2021- Hannah Boekweg
- Amanda J. Guise
- Edward D. Plowey
- Ryan T. Kelly
- Samuel H. Payne
Cited in Scopus: 0In Brief Cellular development and disease progression are gradual transitions between phenotypic stages. Time-course measurements that explicitly measure this transition are important to discover proteome dynamics. Single-cell measurements are a powerful tool for understanding heterogeneity, especially during phenotypic transitions. Single-cell proteomics measurements are emerging as an available tool to characterize the cellular state. We created a statistical method that predicts the success of an experimental design for temporal dynamics. - Research ArticleResearchOpen Access
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane
Molecular & Cellular ProteomicsVol. 20100088Published online: April 29, 2021- Nikolai P. Skiba
- Martha A. Cady
- Laurie Molday
- John Y.S. Han
- Tylor R. Lewis
- William J. Spencer
- and others
Cited in Scopus: 0In Brief The plasma membrane which envelopes the light-sensitive outer segment organelle of vertebrate photoreceptor cells plays diverse roles in supporting photoreceptor function and health. Protein correlation profiling of this membrane revealed a surprisingly small number of unique protein components. Among them are TMEM67 and TMEM237, whose mutations are associated with various syndromic ciliopathies, and embigin found to be associated with the monocarboxylate transporter MCT1. The MCT1–embigin complex likely facilitates lactate transport through this cellular compartment. - Research ArticleResearch Special Issue: ImmunopeptidomicsOpen Access
HLA Class II Presentation Is Specifically Altered at Elevated Temperatures in the B-Lymphoblastic Cell Line JY
Molecular & Cellular ProteomicsVol. 20100089Published online: April 29, 2021- Laura C. Demmers
- Wei Wu
- Albert J.R. Heck
Cited in Scopus: 0In Brief Here the cellular response in a “fever-mimicking state” was investigated by sampling in parallel the proteome and the HLA class I and II ligandomes. Using quantitative proteomics and immunopeptidomics, we found that a proteomic “fever response” is initiated in B-cells after growing the cells for only 3 days at 40 °C and that it is largely mediated by adaptation in the HLA class II rather than HLA class I system.