We request funds to purchase a Nikon A1R Confocal Microscope system to replace our 10 year-old Zeiss/BioRad Radiance system that Zeiss can no longer guarantee to support or repair. The new instrument will be housed within the Program in Membrane Biology (PMB) Microscopy Core at the Massachusetts General Hospital (MGH) in the multidisciplinary Simches Research Center building. The mandate of this MGH- approved Core facility is to provide access to a full range of techniques using microscopy and imaging to individual research groups, 3 NIH funded Centers and 3 Thematic Centers within the MGH community and beyond. Over the past few years, the Core has developed considerable expertise in static and live cell imaging techniques but has fallen behind in providing sophisticated fluorescence methodologies due to the age of our existing equipment and its lack of appropriate laser lines and other hardware options. The three major reasons for this application are: 1) To ensure that we can continue to provide routine confocal microscopy services to our extensive Core user base in the face of an old and potentially non-repairable existing system;2) To expand our Core capabilities to provide state-of-the-art fluorescence modalities including FRET, FRAP and molecular uncaging techniques to our user base;3) To improve our multiwavelength live cell imaging capabilities that are at the moment limited by the absence of appropriate laser lines and poor dual-color sensitivity on our existing 2003 vintage Perkin Elmer spinning disk live cell imaging system. Since the PMB Core was founded in 1986, it has become a central part of the MGH/HMS medical research community. Over 30 NIH-funded PIs and their numerous lab members within the HMS/MGH and in other institutions made significant user of the Core confocal in the past 12 months alone, and we have supported literally hundreds of peer-reviewed publications from our user base over the years. The Core has an ongoing quest to constantly improve and upgrade Core facilities in support of its user base. This has been achieved using funds from NIH SIG applications as well as considerable institutional support from the MGH leadership. Providing our Core user base with continued access to an up-to-date fluorescence imaging platform is essential to maintaining the MGH community at the cutting edge of NIH-funded, health-related research.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR031563-01
Application #
8051380
Study Section
Special Emphasis Panel (ZRG1-CB-J (31))
Program Officer
Levy, Abraham
Project Start
2011-04-01
Project End
2012-03-31
Budget Start
2011-04-01
Budget End
2012-03-31
Support Year
1
Fiscal Year
2011
Total Cost
$561,474
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Bourgeois, Soline; Bounoure, Lisa; Mouro-Chanteloup, Isabelle et al. (2018) The ammonia transporter RhCG modulates urinary acidification by interacting with the vacuolar proton-ATPases in renal intercalated cells. Kidney Int 93:390-402
Battistone, Maria A; Nair, Anil V; Barton, Claire R et al. (2018) Extracellular Adenosine Stimulates Vacuolar ATPase-Dependent Proton Secretion in Medullary Intercalated Cells. J Am Soc Nephrol 29:545-556
Cox, Kimberly H; Oliveira, Luciana M B; Plummer, Lacey et al. (2018) Modeling mutant/wild-type interactions to ascertain pathogenicity of PROKR2 missense variants in patients with isolated GnRH deficiency. Hum Mol Genet 27:338-350
Garza, Jacob C; Qi, Xiaoli; Gjeluci, Klaudio et al. (2018) Disruption of the psychiatric risk gene Ankyrin 3 enhances microtubule dynamics through GSK3/CRMP2 signaling. Transl Psychiatry 8:135
Canali, Susanna; Zumbrennen-Bullough, Kimberly B; Core, Amanda B et al. (2017) Endothelial cells produce bone morphogenetic protein 6 required for iron homeostasis in mice. Blood 129:405-414
Roy, Jeremy; Kim, Bongki; Hill, Eric et al. (2016) Tyrosine kinase-mediated axial motility of basal cells revealed by intravital imaging. Nat Commun 7:10666
Cheung, Pui W; Nomura, Naohiro; Nair, Anil V et al. (2016) EGF Receptor Inhibition by Erlotinib Increases Aquaporin 2-Mediated Renal Water Reabsorption. J Am Soc Nephrol 27:3105-3116
Trepiccione, Francesco; Gerber, Simon D; Grahammer, Florian et al. (2016) Renal Atp6ap2/(Pro)renin Receptor Is Required for Normal Vacuolar H+-ATPase Function but Not for the Renin-Angiotensin System. J Am Soc Nephrol 27:3320-3330