Orbitrap Elite High-Resolution Mass Spectrometer for Proteomics and Metabolomics
Orbitrap Elite High-Resolution Mass Spectrometer for Proteomics and Metabolomics
批准号:
8334735
负责人:
David H Hawke
金额:
$87.74万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-04-22 至 2015-04-21
关键词:
AreaBiological MarkersCancer CenterCancer PatientCancer Research ProjectChargeClinicalComplementDiagnosisDrug TargetingFundingGoalsHousingHumanHybridsIonsLabelMalignant NeoplasmsMalignant neoplasm of brainMalignant neoplasm of ovaryMalignant neoplasm of prostateMass Spectrum AnalysisMedical centerMedicineMolecularOutcomePerformancePost-Translational Protein ProcessingProteinsProteomicsPublic HealthResolutionScanningSpeedStagingSystemTexasUnited StatesUnited States National Institutes of HealthUniversity of Texas M D Anderson Cancer CenterValidationbasecancer therapyimprovedinstrumentmalignant breast neoplasmmass spectrometermetabolomicsmolecular markeroutcome forecastprotein complexprotein metabolitestable isotopevalidation studies
中文摘要
描述(由申请人提供):我们将使用LTQ-Orbitrap Elite(线性离子阱-轨道离子阱混合质谱仪)来支持一系列基础,转化和临床
英文摘要
DESCRIPTION (provided by applicant): We will use the LTQ-Orbitrap Elite (a linear ion-trap-orbital ion-trap hybrid mass spectrometer) to support a range of basic, translational, and clinical
cancer research projects at the University of Texas M. D. Anderson Cancer Center (MDACC) and in collaborative studies in the Texas Medical Center (TMC). The Orbitrap Elite features include high mass resolution (>240,000), large space charge capacity, high mass accuracy (<3 ppm), a mass/charge range of up to 4000 m/z, and dynamic range greater than 103. The documented performance of the Orbitrap Elite exceeds that of most alternative instruments in three critical areas by at least one order of magnitude-resolution, mass accuracy, and scan speed. Those improvements make the Orbitrap the optimal mass spectrometer for proteomic and metabolomic platforms aimed at identification and validation of molecular markers. Its high-resolution, accurate mass capabilities previously could only be achieved with superconducting magnet systems. Importantly, those capabilities have made extraordinary contributions to the analysis of protein complexes, post-translational modifications, and biomarker discovery (identification of previously unidentified proteins and metabolites) as well as early-stage validation studies. The Orbitrap is especially suitable for studies employing stable isotope-dilution mass spectrometry or label-free quantification of proteins or metabolites. We expect that using the Orbitrap for molecular identification studies will imminently improve the diagnosis, treatment, and prognosis of human cancers, in keeping with the goal of the Kleberg Center for Molecular Markers (where the Proteomics Facility is housed) to improve the outcomes of cancer patients. We will use the proposed Orbitrap Elite in support of at least 7 NIH-funded R01, P01, and SPORE grantees and eventually many other NIH-funded projects at MDACC as well as in the TMC. Specifically, we plan to apply this new, improved mass spectrometer to the discovery of protein biomarkers in ongoing projects in breast, brain, ovarian, and prostate cancers. By identifying and validating such biomarkers and helping to identify new drug targets, the instrument will help us improve public health through improvements in the diagnosis and treatment of cancer. It will complement our functional proteomics-based personalized medicine initiatives in the Kleberg Center for Molecular Markers and eventually improve treatment of the large number of cancer patients treated each year at MDACC, the largest and top ranked cancer center in the United States.
期刊论文(9)
专著(0)
科研奖励(0)
会议论文
DOI:
10.15252/msb.20145504
发表时间:
2015-01-21
期刊:
Molecular systems biology
影响因子:
9.9
作者:
[Li X, Wang W, Wang J, Malovannaya A, Xi Y, Li W, Guerra R, Hawke DH, Qin J, Chen J]
通讯作者:
Chen J
DOI:
10.1186/s13073-021-00937-4
发表时间:
2021-08-28
期刊:
Genome medicine
影响因子:
12.3
作者:
[Li Y, Zhang Y, Hu Q, Egranov SD, Xing Z, Zhang Z, Liang K, Ye Y, Pan Y, Chatterjee SS, Mistretta B, Nguyen TK, Hawke DH, Gunaratne PH, Hung MC, Han L, Yang L, Lin C]
通讯作者:
Lin C
DOI:
10.1186/1471-2407-14-44
发表时间:
2014-01-27
期刊:
BMC cancer
影响因子:
3.8
作者:
[Kruger S, Abd Elmageed ZY, Hawke DH, Wörner PM, Jansen DA, Abdel-Mageed AB, Alt EU, Izadpanah R]
通讯作者:
Izadpanah R
海外基金