(from the application): In TRD1, we propose three subprojects that will result in substantial additions to our hardware and software. Collectively, these subprojects will enhance techniques and methods developed at the LFD. TRD1 with its three subprojects is not a mere update or maintenance of instrumentation. On the contrary, each of the subprojects is novel and has its own merits and they are necessary for our DBP's and collaborations.
Specific Aims : During the last five years, fluorescence microscopy has experienced a revolution due to several factors. These factors include better understanding of the physics of optics for achieving super resolution, availability of new types of sensitive detectors, use of computers as an integral part of the microscope, development of light sheet techniques, multi foci multiphoton excitation and the availability of new fluorescent probes, both synthetically produced (quantum dots) and genetically encoded, that offer better brightness and photochemical stability. Consequently, fluorescence microscopy has evolved into a sophisticated technique. Today, there is a major effort to exploit these new capabilities to address urgent problems in cell biology. Imaging methods have become advanced to the point that single molecule detection inside the cell is feasible. One major challenge is the development of methodologies to extract information from the natural systems where all of the biological actions occur simultaneously. The three subprojects address different needs that are not generally found in current efforts for increasing the microscope performance but rather are targeting specific applications that are important for the LFD. These subprojects form a cohesive plan formulated to achieve new quantitative measurements in microscopy.

Public Health Relevance

The proposed technological developments are relevant to a growing number of problems in biomedical research that require real time detection and localization of molecular interactions in 3D in live cells and tissues at the single molecule level. The visualization analysis program developed in this application allows single cells analyses of metabolic indices of cells in the context of tissues, a significant advance in tissue analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Biotechnology Resource Grants (P41)
Project #
2P41GM103540-31
Application #
9073014
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Sammak, Paul J
Project Start
1997-08-01
Project End
2021-06-30
Budget Start
2016-07-25
Budget End
2017-06-30
Support Year
31
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Biomedical Engineering
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92617
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