apipelinefortheidentificationofintactNglycopeptides(六)

Figure 4. Comparison of different decoy strategies. The estimated FDR of each decoy method is compared with the real FDR. “Decoy: + 11” means increasing the mass of each Y ion by 11 Da, and “Decoy: + [1, 30]” means increasing the mass of each Y ion by a random mass ranging from 1–30 Da. “Decoy: Reverse” is simply reversing the Y ions. The finite mixture model is employed for all these decoy meth......阅读全文

a-pipeline-for-the-identification-of-intact-Nglycopeptides(六)

  Figure 4. Comparison of different decoy strategies. The estimated FDR of each decoy method is compared with the real FDR. “Decoy: + 11” means in

a-pipeline-for-the-identification-of-intact-Nglycopeptides(七)

Complementary ion information provided by HCD- and CID-MS/MS. Both HCD- and CID-MS/MScould be used to optimize the glycopeptide identification. Rece

a-pipeline-for-the-identification-of-intact-Nglycopeptides(一)

pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCDand CID-MS/MS and MS3 Wen-Feng Zeng1,2,*, Ming-Qi Liu3,*, Yang Zhang3,

a-pipeline-for-the-identification-of-intact-Nglycopeptides(五)

Alignment between MS/MS and MS3 identifications. Glycans were identified after analyzing the HCD/CID-MS/MS spectrum pairs, but the sequences of pe

a-pipeline-for-the-identification-of-intact-Nglycopeptides(二)

Methods Materials. A uniform mixture of six standard glycoproteins was used as the starting material, including IgG (56834, catalog numeber), IgA

a-pipeline-for-the-identification-of-intact-Nglycopeptides(四)

Interpretation of MS3 data. MS3 data were converted to “.ms3” format by pXtract within pFind Studio (version 2.8)26,27, and then analyzed by pFind

a-pipeline-for-the-identification-of-intact-Nglycopeptides(三)

Figure 1. The overall workflow of pGlyco. First the sample is analyzed by HCD-MS/MS (NCE = 40%).Then the product-dependent CID-MS/MS and data-depend

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites六

N-glycosylation modification of proteins has reported to improve the health of living organisms through antibacterial activity [68], antioxidant a

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites四

Figure 2 Distribution of N-glycopeptides analyzed by different enriched methods and instruments of royal jelly proteins. A is the distribution of N-

An-Integrative-Procedure-for-Apoptosis-Identification-and-Measurement

IntroductionApoptosis is a normal physiological phenomenon put forward by Kerr [1]. It plays an important role in embryonic development, maintenance o

CarbohydrateSpecific-Adhesion-of-Intact-Cells-to-Resolved-Glycolipids-on-T

Carbohydrate-Specific Adhesion of Intact      Cells to Resolved Glycolipids on TLC PlatesRonald L. Schnaar~Professor, Johns Hopkins University Medical

Identification-and-expansion-of-the-tumorigenic-lung-cancer-stem-cell-...

Identification and expansion of the tumorigenic lung cancer stem cell populationLung cancer contains a rare population of CD133+ cancer stem-like ce

A-Yeast-Secretion-Trap-Assay-for-Identification-of-Secreted-Proteins-...

Secreted proteins from plants and phytopathogens play important roles in their interactions and contribute to elaborate mechanisms of attack, defe

An-Integrative-Procedure-for-Apoptosis-Identification-and-Measurement2

TroubleshootingCritical Steps(1) Don’t trypsinize cells for too long when collecting them.(2) Rotation speed should be no more than 1500 rpm during ce

Interleukin6-Induced-Acute-Phenotypic-Microenvironment-Promote...(三)

 Target analysis by Parallel reaction monitoring (PRM)The targeted quantification and verification were carried out in 94 serum samples with 5~6 mic

Identification-of-a-Mutant-Kinase/ATP-Analog-Pair2

Cellular Transfection and Immunoprecipitation  Before proceeding with the experiments outlined below, all kinase pocket mutants should be characterize

Identification-of-a-Mutant-Kinase/ATP-Analog-Pair1

Identification of a Mutant Kinase/ATP Analog PairScott T. Eblen, N. Vinay Kumar, and Michael J. WeberDepartment of Microbiology and Cancer Center, Uni

Comparative-assessment-of-glycosylation-of-recombinant-human-...(一)

Comparative assessment of glycosylation of recombinant human FSH and highly purified FSHHong Wang, Xi Chen, Xiaoxi Zhang, Wei Zhang, Yan Li, Hongrui Y

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites九

41. Schmidt O, Theopold U, Strand M: Innate immunity and its evasion and suppression by hymenopteran endoparasitoids. BioEssays 2001, 23(4):344–35

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites一

Comprehensive identification of novel proteins and N-glycosylation sites in royal jellyLan Zhang1,2†, Bin Han1†, Rongli Li1, Xiaoshan Lu1,3, Aiying Ni

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites八

References1. Fujita T, Kozuka-Hata H, Ao-Kondo H, Kunieda T, Oyama M, Kubo T: Proteomic analysis of the royal jelly and characterization of the fu

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites七

Data analysisTandem mass spectra were retrieved using Xcalibur (version 2.2, Thermo Fisher Scientific) and AnalystTF (version 1.6, AB SCIEX) softw

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites三

 Note: All of the identified proteins are from Apis mellifera. Accession is the unique number given to mark the entry of a protein in the database

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites二

ResultsIdentified novel royal jelly proteins  To expand the number of known proteins in the RJ proteome, RJ proteins were extracted and digested wit

Comprehensive-identification-of-novel-proteins-and-Nglycosylation-sites五

RJ provides efficient energetic fuels for the fast development of larvae and the egg-laying queen through the metabolism of sugars, lipids, and pr

GenomeWide-Identification-of-Transcription-FactorBinding-Sites-in...

Genome-Wide Identification of Transcription Factor-Binding Sites in Plants Using Chromatin Immunoprecipitation Followed by Microarray (ChIP-chip)

Pipeline血流导向装置治疗颅内大型动脉瘤诊疗分析

随着神经介入技术和器械的发展,中小型颅内动脉瘤的介入治疗效果确切,而大型或巨大型动脉瘤的介入治疗效果不满意,其中重要的原因是动脉瘤复发。近年来,随着载瘤动脉重建概念的提出,一种新型的血流导向装置Pipleline应运而生。有研究表明,血流导向装置主要用于治疗未破裂的宽颈动脉瘤、梭型动脉瘤及大型或巨大

Pipeline血流导向装置治疗大脑中动脉复杂动脉瘤的初步...

Pipeline血流导向装置治疗大脑中动脉复杂动脉瘤的初步经验大脑中动脉瘤是颅内动脉瘤的常见类型,采用开颅夹闭及弹簧圈栓塞(或支架辅助)多可获得满意疗效。对于大脑中动脉复杂动脉瘤,包括大型、巨大型、梭形、复发、宽颈动脉瘤及瘤颈钙化、动脉瘤或瘤颈有重要分支血管发出的动脉瘤等,采用支架辅助下弹簧圈栓塞难

血流导向装置Pipeline治疗以单侧眼睑下垂为首发表现的...

血流导向装置Pipeline治疗以单侧眼睑下垂为首发表现的颈内动脉巨大动脉瘤病例分析Pipeline血流导向装置(Pipeline embolization device,PED)主要用于血管腔内治疗成人颈内动脉岩骨段至垂体上动脉开口处近端的大型或巨大宽颈动脉瘤,对于超适应证范围的,如后循环动脉瘤、

Comparative-assessment-of-glycosylation-of-recombinant-human-...(二)

Experimental sectionChemicals and reagentsOne lot of PuregonR-HP of 50 IU/0.5mL and two lots of PuregonR-HP of 100 IU/0.5mL (rhFSH) (Organon, Oss, N