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Jihong Bai

Jihong Bai

· Professor

University of Washington · Bioengineering

Active 1998–2024

h-index39
Citations5.1k
Papers9120 last 5y
Funding$9.5M1 active
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About

Jihong Bai is a professor affiliated with the Fred Hutch Cancer Center and the University of Washington, specializing in biological physics, structure, and design. His research focuses on understanding how neurons are integrated into functional circuits, with particular emphasis on synaptic activity that supports information delivery and storage in the brain. He employs a combination of genetic, biochemical, and electrophysiological techniques to explore synaptic modulation, with a specific interest in the protein machinery that controls exocytosis and endocytosis of synaptic vesicles. His work involves using time-resolved assays to study molecular actions in vitro and electrophysiological methods to monitor neuronal activity in vivo, aiming to uncover structural principles that enable proteins to shape intracellular membranes at synapses. His goal is to develop a molecular understanding of synaptic machinery that can lead to novel strategies for tuning neuronal communication and brain activity.

Research topics

  • Biology
  • Chemistry
  • Cell biology
  • Biochemistry
  • Computer Science
  • Neuroscience
  • Biophysics

Selected publications

  • Presynaptic autophagy is coupled to the synaptic vesicle cycle via ATG-9

    Neuron · 2022 · 104 citations

    • Neuroscience
    • Chemistry
    • Biology
  • A novel dual Ca2+ sensor system regulates Ca2+-dependent neurotransmitter release

    The Journal of Cell Biology · 2021 · 23 citations

    • Biophysics
    • Cell biology
    • Biology

    Ca2+-dependent neurotransmitter release requires synaptotagmins as Ca2+ sensors to trigger synaptic vesicle (SV) exocytosis via binding of their tandem C2 domains-C2A and C2B-to Ca2+. We have previously demonstrated that SNT-1, a mouse synaptotagmin-1 (Syt1) homologue, functions as the fast Ca2+ sensor in Caenorhabditis elegans. Here, we report a new Ca2+ sensor, SNT-3, which triggers delayed Ca2+-dependent neurotransmitter release. snt-1;snt-3 double mutants abolish evoked synaptic transmission, demonstrating that C. elegans NMJs use a dual Ca2+ sensor system. SNT-3 possesses canonical aspartate residues in both C2 domains, but lacks an N-terminal transmembrane (TM) domain. Biochemical evidence demonstrates that SNT-3 binds both Ca2+ and the plasma membrane. Functional analysis shows that SNT-3 is activated when SNT-1 function is impaired, triggering SV release that is loosely coupled to Ca2+ entry. Compared with SNT-1, which is tethered to SVs, SNT-3 is not associated with SV. Eliminating the SV tethering of SNT-1 by removing the TM domain or the whole N terminus rescues fast release kinetics, demonstrating that cytoplasmic SNT-1 is still functional and triggers fast neurotransmitter release, but also exhibits decreased evoked amplitude and release probability. These results suggest that the fast and slow properties of SV release are determined by the intrinsically different C2 domains in SNT-1 and SNT-3, rather than their N-termini-mediated membrane tethering. Our findings therefore reveal a novel dual Ca2+ sensor system in C. elegans and provide significant insights into Ca2+-regulated exocytosis.

  • Dopamine receptor DOP-1 engages a sleep pathway to modulate swimming in C. elegans

    iScience · 2021 · 14 citations

    Senior authorCorresponding
    • Computer Science
    • Neuroscience
    • Cell biology

    . The temporal transition between DOP-3 and DOP-1 pathways highlights the dynamic nature of neuromodulation for rhythmic movements that persist over time.

Recent grants

Frequent coauthors

  • Edwin R. Chapman

    Howard Hughes Medical Institute

    35 shared
  • Yongming Dong

    Fred Hutch Cancer Center

    24 shared
  • Ithai Rabinowitch

    Hebrew University of Jerusalem

    21 shared
  • Yan Liu

    Shandong Agricultural University

    17 shared
  • Vadim A. Klenchin

    University of Wisconsin–Madison

    16 shared
  • Ivan Rayment

    University of Wisconsin–Madison

    16 shared
  • Kumud R. Poudel

    Fred Hutch Cancer Center

    16 shared
  • Gerard Marriott

    University of California, Berkeley

    16 shared

Education

  • Ph.D., Biophysics

    University of Washington

    1995
  • M.S., Physics

    University of Science and Technology of China

    1990
  • B.S., Physics

    University of Science and Technology of China

    1987

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