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Da-Ting Lin, Ph.D.

 

Email: dlin13@jhu.edu

 

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dl

Education

 

Changes in synaptic strength and neuronal connectivity are thought to be important for higher brain functions such as learning and memory. The majority of fast excitatory synaptic transmission in the brain is mediated by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors (AMPARs). The dynamic equilibrium of AMPARs trafficking in and out of synapses plays a critical role in the determination of the strength of each synapse. Several neuronal proteins, such as 4.1N and SAP97, are known to bind to the C-terminus of AMPARs and these intracellular binding partners of AMPARs are likely to play important roles in regulating AMPAR synaptic trafficking. Receptor trafficking is a dynamic process, and directly visualizing different steps of receptor trafficking using optical imaging approach would allow one to better understand the underlying mechanisms that regulate these processes. As a graduate student I gained extensive experience with various optical imaging techniques in the laboratory of Dr. James D. Lechleiter. Since I joined Dr. Richard L. Huganir's laboratory in 2003 as a postdoc fellow, I have set up and applied various optical imaging techniques, in combination with molecular, cellular, biochemical, as well as electrophysiological techniques, to examine different aspects of AMPAR trafficking. The following are some of the optical imaging techniques I used in my research:

 

in vivo In vivo Two-Photon Imaging and Intrinsic Optical Signal Imaging
Probing function of individual dendritic spines with combined two-photon imaging and two-photon uncaging of MNI-caged-L-glutamate
Long-term imaging of neuronal development
Imaging AMPAR endocytosis and recycling
Imaging individual AMPAR insertion using TIR-FM
Examining AMPAR surface diffusion dynamics with sub-resolution single particle tracking using QDot labeling
   

AMPAR trafficking: synthesis, transport, insertion, diffusion, endocytosis, recycling, and degradation.

 

   

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