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Sarah Shahmoradian, Ph.D.

Sarah Shahmoradian, Ph.D.

Assistant Professor

School
Medical School
Department
Center for Alzheimer's and Neurodegenerative Diseases | Biophysics | Peter O'Donnell Jr. Brain Institute
Graduate Programs
Molecular Biophysics
  • Biography

    Download Curriculum Vitae

    Sarah Shahmoradian, born and raised in Richmond, Virginia, received her Ph.D. in Molecular Physiology and Biophysics from Baylor College of Medicine in 2013, under mentorship of Wah Chiu, now at Stanford. She used cryo-electron microscopy (cryo-EM) and tomography (cryo-ET) to reveal structural mechanisms behind the aggregation and modulation of key proteins in neurodegeneration. Her research explained how the chaperonin TRiC/CCT inhibits Huntingtin protein aggregation, how specific protein domains influence these aggregates in Huntington's disease, and how pathological alpha-synuclein aggregates nucleate in a reductionist system of Parkinson's disease.

    As a Roche Postdoctoral Fellow in Henning Stahlberg's lab at the Biozentrum University of Basel, co-mentored by Matthias Lauer and Markus Britschgi at Roche Innovation Center Basel, Shahmoradian and her colleagues discovered that membranes and lipidic material are central to Lewy bodies and Lewy neurites in Parkinson's disease. These findings, validated through various biophysical and biochemical techniques, led to a major reevaluation of these pathological structures that emphasizes alpha-synuclein-lipid interactions. This research has informed the development of more accurate cellular models and strategies for small molecule design in imaging and therapy.

    Currently, the Shahmoradian lab uses advanced imaging techniques, including cryo-ET and correlative light and electron microscopy (CLEM), to investigate how proteins prone to aggregation and their interactions with lipids affect processes at the synapse and endoplasmic reticulum (ER) in health and disease. Her lab aims to understand the macromolecular basis of protein aggregation and membrane remodeling in neuronal diseases within functional neuronal systems. They also innovate by developing new interfaces and technologies to advance EM-based techniques.

  • Research Interest
    • Cryo-electron tomography
    • Micro and Nanoengineering
    • Neurodegeneration
    • Protein aggregation
  • Publications

    Star Featured Publications

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    TorsinA is essential for neuronal nuclear pore complex localization and maturation.
    Kim S, Phan S, Tran HT, Shaw TR, Shahmoradian SH, Ellisman MH, Veatch SL, Barmada SJ, Pappas SS, Dauer WT, Nat Cell Biol 2024 Aug
    Docking for Molecules That Bind in a Symmetric Stack with SymDOCK.
    Smith MS, Knight IS, Kormos RC, Pepe JG, Kunach P, Diamond MI, Shahmoradian SH, Irwin JJ, DeGrado WF, Shoichet BK, J Chem Inf Model 2024 Jan 64 2 425-434
    Docking for molecules that bind in a symmetric stack with SymDOCK.
    Smith MS, Knight IS, Kormos RC, Pepe JG, Kunach P, Diamond MI, Shahmoradian SH, Irwin JJ, DeGrado WF, Shoichet BK, bioRxiv 2023 Oct
    Cryo-EM structure of Alzheimer's disease tau filaments with PET ligand MK-6240.
    Kunach P, Vaquer-Alicea J, Smith MS, Hopewell R, Monistrol J, Moquin L, Therriault J, Tissot C, Rahmouni N, Massarweh G, Soucy JP, Guiot MC, Shoichet BK, Rosa-Neto P, Diamond MI, Shahmoradian SH, bioRxiv 2023 Sep
    Cryo-electron tomography provides topological insights into mutant huntingtin exon 1 and polyQ aggregates.
    Galaz-Montoya JG, Shahmoradian SH, Shen K, Frydman J, Chiu W, Commun Biol 2021 07 4 1 849
    A Compartmentalized Neuronal Cell-Culture Platform Compatible With Cryo-Fixation by High-Pressure Freezing for Ultrastructural Imaging.
    Tran HT, Lucas MS, Ishikawa T, Shahmoradian SH, Padeste C, Front Neurosci 2021 15 726763