1.Proteomics and peptidomics analysis of Sepiae Endoconcha.
Rui LIU ; Shuang WEI ; Xin-Zhi WANG ; Jian-Ming CHENG ; Hao WU
China Journal of Chinese Materia Medica 2020;45(16):3883-3889
Shotgun based proteomics and peptidomics analysis were used to investigate the proteins and peptides in marine traditional Chinese medicine(TCM) Sepiae Endoconcha(cuttlebone). Peptides were extracted from cuttlebone by acidified methanol, and then strong cation exchange(SCX) resin was used to enrich those peptides. Also, proteins from cuttlebone were extracted and digested by trypsin. nano-LC Q Exactive Orbitrap mass spectrometry was used to analyze proteins and peptides from cuttlebone. As a result, a total of 16 proteins and 168 peptides were identified by protein database search, and 328 peptides were identified by De novo sequencing. The identified proteins were hemocyanin, enolase, myosin, actin, calmodulin, etc., and the identified peptides were derived from actin, histone, and tubulin. All these proteins and peptides were important components in cuttlebone, which would provide important theoretical and research basis for marine TCM cuttlebone investigations.
Cations
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Databases, Protein
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Mass Spectrometry
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Peptides
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Proteomics
2.Network pharmacological study of Schizonepetae Herba and Saposhnikoviae Radix in treatment of ulcerative colitis.
Ying QU ; Shu-Xin ZHANG ; Lu ZHOU ; Li-Yuan FU ; Zi-Hao LIU ; Shi-Ying LI ; Ting-Ting DAI ; Xiang-Yang YANG ; Hui-Ru JI ; Min-Ran CAO
China Journal of Chinese Materia Medica 2019;44(24):5465-5472
The aim of this paper was to screen the active targets of Schizonepetae Herba and Saposhnikoviae Radix in the treatment of ulcerative colitis by means of network pharmacology,and to investigate their mechanism of action. The effective components of Schizonepetae Herba and Saposhnikoviae Radix were screened out by traditional Chinese medicine systematic pharmacological( TCMSP)database,with oral bioavilability( OB) ≥30% and drug-like( DL) ≥18% selected as the thresholds. Target PPI network was built between the main components and their corresponding targets. One hundred and eighty-two human genes corresponding to the medicine target sites were obtained from Uniprot database; 3 874 genes corresponding to ulcerative colitis were obtained from Genecard database.A total of 115 intersection genes were screened from disease genes and medicine genes,and the PPI interaction analysis was conducted by using String tool. Disease-target PPI network was drawn by using Cytoscape software,and component-target-disease network was constructed. One hundred and eight nodes and 1 882 connections were found,and then Cytoscape software was used to merge the networks and filter the core network for gene GO function analysis and KEGG pathway enrichment analysis. The mechanism of Schizonepetae Herba and Saposhnikoviae Radix was then verified by animal experiment. Gene GO functional analysis suggested that biological process,molecular functions and cell components were involved,and it was found that ulcerative colitis might be related to transcription factor activity,and cytokine receptor binding,etc. Gene KEGG pathway enrichment analysis showed that the mechanism of ulcerative colitis might be associated with TNF and Toll-like receptors( TLRs) signaling pathway-mediated cytoinflammatory factors interleukin-1( IL-1) and interleukin-6( IL6). The possible mechanism of the effective components of Schizonepetae Herba and Saposhnikoviae Radix in treating ulcerative colitis might be related to intervening the cytokine receptor binding of TNF and TLRs signaling pathways,reducing the transcription of nuclear factor-kappaB( NF-κB),and inhibiting the secretion of intestinal inflammatory factors IL-1 and IL-6.
Animals
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Apiaceae/chemistry*
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Colitis, Ulcerative/drug therapy*
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Databases, Genetic
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Drugs, Chinese Herbal/therapeutic use*
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Humans
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Interleukins/metabolism*
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Lamiaceae/chemistry*
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Medicine, Chinese Traditional
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Phytotherapy
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Plant Roots/chemistry*
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Protein Interaction Mapping
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Signal Transduction
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Software
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Toll-Like Receptors/metabolism*
3.In silico analysis of putative drug and vaccine targets of the metabolic pathways of Actinobacillus pleuropneumoniae using a subtractive/comparative genomics approach
Biruk T BIRHANU ; Seung Jin LEE ; Na Hye PARK ; Ju Beom SONG ; Seung Chun PARK
Journal of Veterinary Science 2018;19(2):188-199
Actinobacillus pleuropneumoniae is a Gram-negative bacterium that resides in the respiratory tract of pigs and causes porcine respiratory disease complex, which leads to significant losses in the pig industry worldwide. The incidence of drug resistance in this bacterium is increasing; thus, identifying new protein/gene targets for drug and vaccine development is critical. In this study, we used an in silico approach, utilizing several databases including the Kyoto Encyclopedia of Genes and Genomes (KEGG), the Database of Essential Genes (DEG), DrugBank, and Swiss-Prot to identify non-homologous essential genes and prioritize these proteins for their druggability. The results showed 20 metabolic pathways that were unique and contained 273 non-homologous proteins, of which 122 were essential. Of the 122 essential proteins, there were 95 cytoplasmic proteins and 11 transmembrane proteins, which are potentially suitable for drug and vaccine targets, respectively. Among these, 25 had at least one hit in DrugBank, and three had similarity to metabolic proteins from Mycoplasma hyopneumoniae, another pathogen causing porcine respiratory disease complex; thus, they could serve as common therapeutic targets. In conclusion, we identified glyoxylate and dicarboxylate pathways as potential targets for antimicrobial therapy and tetra-acyldisaccharide 4′-kinase and 3-deoxy-D-manno-octulosonic-acid transferase as vaccine candidates against A. pleuropneumoniae.
Actinobacillus pleuropneumoniae
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Actinobacillus
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Computer Simulation
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Cytoplasm
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Databases, Protein
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Drug Resistance
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Genes, Essential
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Genome
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Genomics
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Incidence
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Metabolic Networks and Pathways
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Mycoplasma hyopneumoniae
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Pleuropneumonia
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Respiratory System
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Swine
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Transferases
4.Network pharmacology study of Xiaoxuming Decoction based on vasodilatory and vasoconstrictory related GPCR targets.
Wen-Dan LU ; Li LI ; Yan-Jia SHEN ; Rui ZHOU ; Ran YANG ; Xiao-Cong PANG ; Guan-Hua DU
China Journal of Chinese Materia Medica 2018;43(23):4698-4708
In this study, bioinformatics methods such as molecular docking and network pharmacology were adopted to establish Xiaoxuming Decoction (XXMD) "compound-vasodilatory and vasoconstrictory related G protein-coupled receptors (GPCR) targets" network, then the vascular function regulatory effective components and the potential targets of XXMD were analyzed. Based on the XXMD herb sources, the chemical structures of the compounds were retrieved from the national scientific data sharing platform for population and health pharmaceutical information center, TCMSP database and the latest research literatures. The chemical molecular library was established after class prediction and screening for medicinal and metabolic properties. Then, five kinds of vasodilatory and vasoconstrictory related GPCR crystal structure including 5-HT receptors (5-HT1AR, 5-HT1BR), AT1R, β2-AR, hUTR and ETB were retrieved from RCSB Protein Data Bank database or constructed by homology modeling of Discovery Studio 4.1 built-in modeling tools. After virtual screening by Libdock molecular docking, the highest rated 50 compounds of each target were collected and analyzed. The collected data were further used to construct and analyze the network by Cytoscape 3.4.0. The results showed that most of the chemical composition effects were associated with different vasodilatory and vasoconstrictory related GPCR targets, while a few effective components could be applied to multiple GPCR targets at the same time, therefore forming synergies and vasorelaxant effects of XXMD.
Databases, Protein
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Drugs, Chinese Herbal
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Models, Chemical
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Molecular Docking Simulation
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Receptors, G-Protein-Coupled
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metabolism
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Vasodilation
5.PTMD: A Database of Human Disease-associated Post-translational Modifications.
Haodong XU ; Yongbo WANG ; Shaofeng LIN ; Wankun DENG ; Di PENG ; Qinghua CUI ; Yu XUE
Genomics, Proteomics & Bioinformatics 2018;16(4):244-251
Various posttranslational modifications (PTMs) participate in nearly all aspects of biological processes by regulating protein functions, and aberrant states of PTMs are frequently implicated in human diseases. Therefore, an integral resource of PTM-disease associations (PDAs) would be a great help for both academic research and clinical use. In this work, we reported PTMD, a well-curated database containing PTMs that are associated with human diseases. We manually collected 1950 known PDAs in 749 proteins for 23 types of PTMs and 275 types of diseases from the literature. Database analyses show that phosphorylation has the largest number of disease associations, whereas neurologic diseases have the largest number of PTM associations. We classified all known PDAs into six classes according to the PTM status in diseases and demonstrated that the upregulation and presence of PTM events account for a predominant proportion of disease-associated PTM events. By reconstructing a disease-gene network, we observed that breast cancers have the largest number of associated PTMs and AKT1 has the largest number of PTMs connected to diseases. Finally, the PTMD database was developed with detailed annotations and can be a useful resource for further analyzing the relations between PTMs and human diseases. PTMD is freely accessible at http://ptmd.biocuckoo.org.
Databases, Protein
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Disease
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genetics
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Gene Regulatory Networks
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Humans
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Phosphorylation
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Protein Processing, Post-Translational
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Proteins
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metabolism
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Search Engine
6.TSNAdb: A Database for Tumor-specific Neoantigens from Immunogenomics Data Analysis.
Jingcheng WU ; Wenyi ZHAO ; Binbin ZHOU ; Zhixi SU ; Xun GU ; Zhan ZHOU ; Shuqing CHEN
Genomics, Proteomics & Bioinformatics 2018;16(4):276-282
Tumor-specific neoantigens have attracted much attention since they can be used as biomarkers to predict therapeutic effects of immune checkpoint blockade therapy and as potential targets for cancer immunotherapy. In this study, we developed a comprehensive tumor-specific neoantigen database (TSNAdb v1.0), based on pan-cancer immunogenomic analyses of somatic mutation data and human leukocyte antigen (HLA) allele information for 16 tumor types with 7748 tumor samples from The Cancer Genome Atlas (TCGA) and The Cancer Immunome Atlas (TCIA). We predicted binding affinities between mutant/wild-type peptides and HLA class I molecules by NetMHCpan v2.8/v4.0, and presented detailed information of 3,707,562/1,146,961 potential neoantigens generated by somatic mutations of all tumor samples. Moreover, we employed recurrent mutations in combination with highly frequent HLA alleles to predict potential shared neoantigens across tumor patients, which would facilitate the discovery of putative targets for neoantigen-based cancer immunotherapy. TSNAdb is freely available at http://biopharm.zju.edu.cn/tsnadb.
Antigens, Neoplasm
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metabolism
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Data Analysis
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Databases, Genetic
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Humans
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Immunotherapy
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Mutation
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genetics
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Neoplasms
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genetics
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immunology
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Tumor Suppressor Protein p53
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genetics
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Urinary Bladder Neoplasms
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genetics
7.Trends and Patterns of Hepatocellular Carcinoma Treatment in Korea.
Young Mi HONG ; Ki Tae YOON ; Mong CHO ; Dae Hwan KANG ; Hyung Wook KIM ; Cheol Woong CHOI ; Su Bum PARK ; Jeong HEO ; Hyun Young WOO ; Won LIM
Journal of Korean Medical Science 2016;31(3):403-409
Multiple therapeutic modalities are available for hepatocellular carcinoma (HCC) treatment. We aimed to evaluate the trends for HCC treatment in Korea. Recent trends and patterns in treatment modalities were assessed in HCC patients who first registered for the Health Insurance Review Assessment Service between 2008 and 2012. From 2009 to 2012, 57,690 patients were diagnosed with HCC. Transcatheter arterial chemoembolization (TACE) was the most common treatment modality for initial treatment. Curative treatment modalities like hepatic resection, liver transplantation, and local ablation therapy increased gradually. The 3 most common treatment modalities (hepatic resection, local ablation therapy, TACE) used after initial treatment in 2009 were studied. Following initial hepatic resection, 44.5% of patients required re-treatment. TACE was the most common modality (in 48.3% of cases), while 15.0% of patients received local ablation therapy. After local ablation therapy, 55.4% of patients were re-treated, wherein 45.0% of patients received TACE and 31.5% received local ablation therapy. Following initial TACE, 73.9% patients were re-treated, most commonly with TACE (57.7%) followed by local ablation therapy (12.8%). While there were no significant differences between the initial and re-treatment modalities, various multiple treatments followed the initial treatment. The treatment modalities were interchangeable.
Aged
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Carcinoma, Hepatocellular/epidemiology/pathology/*therapy
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Chemoembolization, Therapeutic
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Combined Modality Therapy/trends
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Cross-Sectional Studies
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Databases, Factual
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Female
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Humans
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Insurance Claim Review
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Liver Neoplasms/epidemiology/pathology/*therapy
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Liver Transplantation
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Male
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Middle Aged
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Niacinamide/administration & dosage/analogs & derivatives
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Phenylurea Compounds/administration & dosage
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Prevalence
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Protein Kinase Inhibitors/administration & dosage
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Republic of Korea/epidemiology
8.Quaternion-based Characterization of Protein α Helix.
Journal of Biomedical Engineering 2016;33(1):155-160
This paper proposes a method based on quaternion for characterization a helix of proteins. The method defines the parameter called Quaternion Helix Axis Spherical Distance (QHASD) on the basis of mapping protein Cα frames' helical axis onto a unit sphere, and uses QHASD to characterize the a helix of the protein secondary structure. Application of this method has been verified based on the PDBselect database, with an a helix characterization accuracy of 91.7%. This method possesses significant advantages of high detection accuracy, low computation and clear geometric significance.
Algorithms
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Databases, Protein
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Models, Molecular
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Protein Structure, Secondary
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Proteins
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chemistry
10.Protein Interaction Network Construction and Biological Pathway Analysis Related to Atherosclerosis.
Quhuan LI ; Shanshan GU ; Na LI ; Zhenyang LI ; Wenlong LAI ; Yang ZENG
Journal of Biomedical Engineering 2015;32(6):1255-1260
Atherosclerosis is a complex disease characterized by lipid accumulation in the vascular wall and influenced by multiple genetic and environmental factors. To understand the mechanisms of molecular regulation related to atherosclerosis better, a protein interaction network was constructed in the present study. Genes were collected in nucleotide database and interactions were downloaded from Biomolecular Object Network Database (BOND). The interactional data were imported into the software Cytoscape to construct the interaction network, and then the degree characteristics of the network were analyzed for Hub proteins. Statistical significance pathways and diseases were figured out by inputting Hub proteins to KOBAS2. 0. The complete pathway network related to atherosclerosis was constructed. The results identified a series of key genes related to atherosclerosis, which would be the potential promising drug targets for effective prevention.
Atherosclerosis
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genetics
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Databases, Factual
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Humans
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Protein Interaction Mapping
;
methods
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Protein Interaction Maps
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Software

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