The Boston University Mass Spectrometry Resource for Biology and Medicine serves as the successor to the MIT Resource. The BUSM Resource will assume many of the assets of the MIT Resource in terms of both personnel and equipment and take on its responsibilities. C.E. Costello and V.N. Reinhold, Harvard School of Public health, have joined their research efforts and serve as Director and Associate Director, respectively, of the new Resource. This combination of former MIT and Harvard School of Public health laboratories provides a strong base for the BUSM MS Resource, and makes efficient use of research funds by bringing together complementary experience and equipment and avoiding potential redundancies. The goals of the BUSM MS Resource are: 1) advancement of mass spectrometric methods and instrumentation to meet established needs in biochemistry and medicine, 2) identification of new areas appropriate for MS in the health sciences, 3) development of new MS-based approaches to meet the requirements of these fields, 4) application of cutting-edge MS to the solution of critical questions in the life sciences, 5) training of students, postdoctoral fellows and practicing scientists in mass spectrometry, and 6) education of the local, national and international community about modern mass spectrometry to encourage its wide and appropriate use. Goals (1) and (3) constitute Technological Research and Development, (4) represents Collaborative and User interactions and (5) includes Training and Dissemination. The focus of activity will be the development and utilization of sensitive and structural-information-rich methods to address fundamental issues in glycobiology at both the research and clinical level; close interactions with colleagues in many disciplines will be encouraged. Mass spectrometric approaches will primarily include electrospray and matrix-assisted laser desorption as ionization methods. The application of Fourier transform ion cyclotron resonance MS to biochemical problems will be explored and its results compared to 4-sector, triple quadrupole and time-of-flight mass analysis. Collaborative and User projects will involve life science investigators throughout the US and abroad.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR010888-03
Application #
2736195
Study Section
Special Emphasis Panel (ZRG3-SSS-6 (12))
Project Start
1996-07-01
Project End
2001-06-30
Budget Start
1998-07-01
Budget End
1999-06-30
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Boston University
Department
Psychiatry
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
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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
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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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