Fourier transform ion cyclotron resonance mass spectrometry (FTMS) developments and applications to the analysis of glycans, peptidoglycans, and proteoglycans are an important component of this research resource. There are two specific aims for this core project: 1. To design, build, test, and apply a vibrationally cooled matrix-assisted laser desorption/ionization Fourier transform ion cyclotron resonance mass spectrometer with a mass filtering quadrupole, and collision/accumulation linear ion trap in the front-end ion optics. 2. To build a small 4.7 T FTMS system for testing ICR cells, ion optics, and electronics. ? ? During the previous grant period, a high-pressure MALDI FT mass spectrometer was constructed and demonstrated to have significant advantages in cooling labile biomolecule ions that are desorbed in the MALDI experiment. The approach has been used extensively in collaborations, providing a good example of the desired """"""""push-pull"""""""" between technological development and collaboration. Although VC-MALDI-FTMS does cool the vibrational excitation and stabilize, it also cools the MALDI adducts formed from matrix and analyte molecules, causing the MS signal to be distributed over additional components, cluttering the spectra and increasing the space charge. In addition, although MALDI ions can be fragmented in this instrument by IRMPD and SORI-CAD, these ergodic methods select the lowest energy pathway, limiting the information content of the fragmentation and preventing cross-ring cleavages of oligosaccharides. ? ? Instrument development such as that proposed in this specific aim is hindered because testing new devices and electronics is slow owing to the extensive pump down that is needed in vacuum recycling. To this end, the construction of a """"""""test-bed"""""""" instrument is proposed. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
2P41RR010888-11
Application #
7242173
Study Section
Special Emphasis Panel (ZRG1-BCMB-H (40))
Program Officer
Sheeley, Douglas
Project Start
1996-07-01
Project End
2012-05-31
Budget Start
2007-08-03
Budget End
2008-05-31
Support Year
11
Fiscal Year
2007
Total Cost
$2,225,248
Indirect Cost
Name
Boston University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Lu, Yanyan; Jiang, Yan; Prokaeva, Tatiana et al. (2017) Oxidative Post-Translational Modifications of an Amyloidogenic Immunoglobulin Light Chain Protein. Int J Mass Spectrom 416:71-79
Sethi, Manveen K; Zaia, Joseph (2017) Extracellular matrix proteomics in schizophrenia and Alzheimer's disease. Anal Bioanal Chem 409:379-394
Hu, Han; Khatri, Kshitij; Zaia, Joseph (2017) Algorithms and design strategies towards automated glycoproteomics analysis. Mass Spectrom Rev 36:475-498
Ji, Yuhuan; Bachschmid, Markus M; Costello, Catherine E et al. (2016) S- to N-Palmitoyl Transfer During Proteomic Sample Preparation. J Am Soc Mass Spectrom 27:677-85
Hu, Han; Khatri, Kshitij; Klein, Joshua et al. (2016) A review of methods for interpretation of glycopeptide tandem mass spectral data. Glycoconj J 33:285-96
Pu, Yi; Ridgeway, Mark E; Glaskin, Rebecca S et al. (2016) Separation and Identification of Isomeric Glycans by Selected Accumulation-Trapped Ion Mobility Spectrometry-Electron Activated Dissociation Tandem Mass Spectrometry. Anal Chem 88:3440-3
Wang, Yun Hwa Walter; Meyer, Rosana D; Bondzie, Philip A et al. (2016) IGPR-1 Is Required for Endothelial Cell-Cell Adhesion and Barrier Function. J Mol Biol 428:5019-5033
Srinivasan, Srimathi; Chitalia, Vipul; Meyer, Rosana D et al. (2015) Hypoxia-induced expression of phosducin-like 3 regulates expression of VEGFR-2 and promotes angiogenesis. Angiogenesis 18:449-62
Yu, Xiang; Sargaeva, Nadezda P; Thompson, Christopher J et al. (2015) In-Source Decay Characterization of Isoaspartate and ?-Peptides. Int J Mass Spectrom 390:101-109
Steinhorn, Benjamin S; Loscalzo, Joseph; Michel, Thomas (2015) Nitroglycerin and Nitric Oxide--A Rondo of Themes in Cardiovascular Therapeutics. N Engl J Med 373:277-80

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