We are continuing to develop a digital feedback tracking system which, in conjunction with our second generation optical trapping rig, will allow us to study the diffusion and directed motion of cell membrane proteins. With this system we will be able to distinguish random diffusion from directed motion, investigate the nature of anomalous diffusion on cell membranes, and gain information on the viscous drag of the membrane and glycocalyx on cell surface proteins. Initial experiments will take place using IgE proteins on RBL cells; later investigations may involve LDL-receptor molecules, NCAMs, or MHC class 1 molecules.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR004224-09
Application #
5224754
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
9
Fiscal Year
1996
Total Cost
Indirect Cost
Migone, Fernando F; Cowan, Robert G; Williams, Rebecca M et al. (2016) In vivo imaging reveals an essential role of vasoconstriction in rupture of the ovarian follicle at ovulation. Proc Natl Acad Sci U S A 113:2294-9
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McMullen, Jesse D; Zipfel, Warren R (2010) A multiphoton objective design with incorporated beam splitter for enhanced fluorescence collection. Opt Express 18:5390-8

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