This proposal requests continued support for the MIT/Harvard Center for Magnetic Resonance (CMR) located at the Francis Bitter Magnet Laboratory, MIT (Grant RR-009995-22). During the coming five year grant period we plan significant upgrades of existing equipment, acquisition of new instrumentation, and research initiatives in several new areas: (1) The 19 spectrometers currently operating in the facility will continue to be improved with new transmitters, receivers, pulse programmers, computers, etc. (2) The facility will expand with the addition of four instruments: (a) a 250 GHz EPR/ENDOR spectrometer, (b) a 375 MHz DNP spectrometer, and (c) a 750 MHz/89 mm magnet and console will be completed, and (d) we plan to pursue acquisition of a 900 MHZ magnet and console. (3) New and continuing areas of interest in the core research program include: (a) RF gradient enhanced spectroscopy, (b) high resolution solution NMR spectroscopy of proteins and protein/nucleic acid complexes, (c) imaging of solids, (d) structural studies of solids via dipolar recoupling techniques, (e) structural studies of large proteins including enzyme/substrate inhibitor complexes, beta- amyloid, bacteriorhodopsin, and halorhodopsin, (f) CW and pulsed dynamic nuclear polarization, and (g) high frequency CW and pulsed EPR and ENDOR studies of paramagnetic enzymes and enzyme inhibitor complex, (4) The collaborative research effort will grow significantly and will include Solution NMR investigations of (a) drug induced DNA degradation (Stubbe), (b) human sarcomas (Singer), (c) intermediates in protein folding (KEMP), (D) combinatorial carbohydrate libraries (Seeberger), (3) ferrodoxins (Pochapsky), (f) protein dynamics (Kern), and (g) structural studies of a number of proteins (Wagner). Imaging studies will include development of a number of new techniques and investigation of new systems. (5) The service component of the facility remains an important function as is evident by the 14 proposals from outside investigators who have or plan to use the facility frequently. (6) Plans for training and dissemination include course work in magnetic resonance seminars, and publication in scholarly journals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Biotechnology Resource Grants (P41)
Project #
8P41EB002026-28
Application #
6639840
Study Section
Special Emphasis Panel (ZRG3-BMT (03))
Program Officer
Mclaughlin, Alan Charles
Project Start
1976-05-01
Project End
2004-04-30
Budget Start
2003-05-01
Budget End
2004-04-30
Support Year
28
Fiscal Year
2003
Total Cost
$1,136,380
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Internal Medicine/Medicine
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Chhabra, Sandeep; Fischer, Patrick; Takeuchi, Koh et al. (2018) 15N detection harnesses the slow relaxation property of nitrogen: Delivering enhanced resolution for intrinsically disordered proteins. Proc Natl Acad Sci U S A 115:E1710-E1719
Mallis, Robert J; Arthanari, Haribabu; Lang, Matthew J et al. (2018) NMR-directed design of pre-TCR? and pMHC molecules implies a distinct geometry for pre-TCR relative to ??TCR recognition of pMHC. J Biol Chem 293:754-766
Hagn, Franz; Nasr, Mahmoud L; Wagner, Gerhard (2018) Assembly of phospholipid nanodiscs of controlled size for structural studies of membrane proteins by NMR. Nat Protoc 13:79-98
Fu, Qingshan; Shaik, Md Munan; Cai, Yongfei et al. (2018) Structure of the membrane proximal external region of HIV-1 envelope glycoprotein. Proc Natl Acad Sci U S A 115:E8892-E8899
Hjortness, Michael K; Riccardi, Laura; Hongdusit, Akarawin et al. (2018) Abietane-Type Diterpenoids Inhibit Protein Tyrosine Phosphatases by Stabilizing an Inactive Enzyme Conformation. Biochemistry 57:5886-5896
Coote, Paul W; Robson, Scott A; Dubey, Abhinav et al. (2018) Optimal control theory enables homonuclear decoupling without Bloch-Siegert shifts in NMR spectroscopy. Nat Commun 9:3014
Wittmann, J J; Can, T V; Eckardt, M et al. (2018) High-precision measurement of the electron spin g factor of trapped atomic nitrogen in the endohedral fullerene N@C60. J Magn Reson 290:12-17
Ji, X; Can, T V; Mentink-Vigier, F et al. (2018) Overhauser effects in non-conducting solids at 1.2?K. J Magn Reson 286:138-142
Iadanza, Matthew G; Silvers, Robert; Boardman, Joshua et al. (2018) The structure of a ?2-microglobulin fibril suggests a molecular basis for its amyloid polymorphism. Nat Commun 9:4517
Liao, Shu Y; Lee, Myungwoon; Hong, Mei (2018) Interplay between membrane curvature and protein conformational equilibrium investigated by solid-state NMR. J Struct Biol :

Showing the most recent 10 out of 281 publications