Acquisition of a Hybrid Quadrupole, Ion Mobility Separation, Orthogonal Accelerat
Acquisition of a Hybrid Quadrupole, Ion Mobility Separation, Orthogonal Accelerat
批准号:
7591899
负责人:
Sheng Zhang
金额:
$50.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-05-01 至 2010-04-30
关键词:
AccelerationAchievementAmino Acid SequenceArtsBiological SciencesChargeComplementComplexCore FacilityDataData QualityEducationFacultyFundingGoalsGrantGrowthHigh Pressure Liquid ChromatographyHybridsLabelLigandsMass Spectrum AnalysisN.I.H. Research SupportPeptide MappingPeptide Sequence DeterminationPositioning AttributePost-Translational Protein ProcessingProcessProtein ConformationProteinsProteomicsPublic HealthRequest for ApplicationsResearchResearch InfrastructureResearch PersonnelResearch Project GrantsResolutionResourcesSamplingScanningShapesSpecificityStable Isotope LabelingStudentsTechnologyTertiary Protein StructureTimeTraining ProgramsUnited States National Institutes of HealthUniversitiesWatercollegecomparativedata acquisitiondomain mappinggenome sequencingimprovedinstrumentinstrumentationinterestion mobilitymass spectrometermolecular sizeprogramsprotein complexpublic health relevancesuccess
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This application requests support for the acquisition of a hybrid Quadrupole, Ion Mobility separation, orthogonal acceleration Time-of-Flight Tandem Mass Spectrometer (Synapt HDMS), interfaced with a fully integrated ultra-high performance liquid chromatography (nanoAcquityUPLC) platform from Waters Corporation. This state-of-the-art instrument will be utilized as a shared research resource in the Cornell Proteomics and Mass Spectrometry (MS) Facility and will be essential to 28 active NIH supported grants. There is a growing interest in proteomics and MS at Cornell, as is evidenced by the exponential growth in the number of samples processed by the facility over the past 3 years (Figure 2). The proposed instrument will complement the existing instrumentation in Cornell, particularly with respect to its applications for analysis of intact protein complexes, protein-protein/ligand interactions and probing protein conformation. This highly sensitive and accurate mass instrument will provide capabilities in protein domain mapping and peptide mapping resulting in confident identification of protein modifications and better de-novo sequencing of proteins for which there is no available genome sequence. This high resolution instrument will be critical to the success of quantitative proteomics studies using stable isotope labeling (SILAC and iTRAQ). The power of UPLC separation combining with MSE scan feature improves the dynamic range of the instrument enhancing the identification of low abundance proteins and enables label-free comparative proteomics. Furthermore, the instrument includes both ion mobility and Time Aligned Parallel (TAP) fragmentation features which will provide increased specificity and more confident structural characterization of proteins and other bio-molecules. The particular strengths of the proposed instrument are: i) Ion Mobility separation which provides a means to estimate molecular size, shape and charge in addition to mass; ii) TAP fragmentation for structural characterization; iii) High mass accuracy (< 2 ppm RMS via the LockSpray), high resolution (17,500) and wide dynamic range (4 orders of linearity) critical for improved data quality; iv) High duty cycle and fast TDC (4GHz) for fast data acquisition rates; v) Wide m/z range (100,000 m/z) for TOF analyzer capable of analysis > 1,000 kDa protein complexes; vi) UPLC-MS/MS with MSE mode for a parallel data acquisition enabling sensitive analysis of complex samples with a wide dynamic concentration of analytes. The proposed instrument will enhance the electrospray MS technologies available in the core facility. The acquisition of this instrument will have an enormous impact on more than two dozens of NIH-funded research projects, and will improve the research infrastructure of Cornell University and the education/training programs of students and researchers. It will accelerate and facilitate a wide range of research projects of Cornell faculty across six colleges relevant to life sciences research, and help to maintain Cornell's competitive position. PUBLIC HEALTH RELEVANCE: The relevance of this application to public health is established through the 28 odd NIH supported research programs that would benefit from the acquisition of this instrumentation. The instrumentation requested herein possesses technical abilities that far exceed those that are currently available to these researchers and thus would allow them to accomplish the goals of these funded projects through the gathering of more and better data. The improved quality and quantity of data gathered in connection with these projects is critical to the achievement of the public health goals for which each was granted priority funding.
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DOI:
10.1002/elps.201200656
发表时间:
2013-08
期刊:
Electrophoresis
影响因子:
2.9
作者:
[Thannhauser TW, Shen M, Sherwood R, Howe K, Fish T, Yang Y, Chen W, Zhang S]
通讯作者:
Zhang S
DOI:
10.1038/nchembio.1609
发表时间:
2014-10
期刊:
Nature chemical biology
影响因子:
14.8
作者:
[Ollis AA, Zhang S, Fisher AC, DeLisa MP]
通讯作者:
DeLisa MP
DOI:
10.1038/srep15237
发表时间:
2015-10-20
期刊:
Scientific reports
影响因子:
4.6
作者:
[Ollis AA, Chai Y, Natarajan A, Perregaux E, Jaroentomeechai T, Guarino C, Smith J, Zhang S, DeLisa MP]
通讯作者:
DeLisa MP
Comparative Phosphoproteomics Reveals an Important Role of MKK2 in Banana (Musa spp.) Cold Signal Network.
比较磷酸化蛋白质组学揭示 MKK2 在香蕉(Musa spp.)冷信号网络中的重要作用
DOI:
10.1038/srep40852
发表时间:
2017-01-20
期刊:
Scientific reports
影响因子:
4.6
作者:
[Gao J, Zhang S, He WD, Shao XH, Li CY, Wei YR, Deng GM, Kuang RB, Hu CH, Yi GJ, Yang QS]
通讯作者:
Yang QS
Use of a stable-isotope-labeled reporter peptide and antioxidants for reliable quantification of methionine oxidation in a monoclonal antibody by liquid chromatography/mass spectrometry.
使用稳定同位素标记的报告肽和抗氧化剂通过液相色谱/质谱法可靠地定量单克隆抗体中的蛋氨酸氧化。
DOI:
10.1002/rcm.7646
发表时间:
2016
期刊:
Rapid communications in mass spectrometry : RCM
影响因子:
--
作者:
[Kang,Pilsoo, Mezhebovsky,Tanya, Chen,Wei, McCardle,JamesA, Zhang,Sheng, Sullivan,EricP, Sass,PhilipM, Routhier,Eric]
通讯作者:
Routhier,Eric
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