Tomas Kirchhausen, Ph.D.

Tomas Kirchhausen, Ph.D.

Senior Investigator, Program in Cellular and Molecular Medicine (Boston Children's Hospital)
Springer Family Professor of Pediatrics (HMS)
Professor of Cell Biology (HMS)

The Kirchhausen Lab focuses on understanding processes that mediate and regulate cellular membrane remodeling, the biogenesis of organelles, and the ways by which viruses, biologicals and oligonucleotides are delivered to the cell interior. 

By direct observation of molecular events obtained using Lattice Light Sheet Microscopy and Lattice Light Sheet Microscopy optimized with Adaptive Optics (AO-LLSM), frontier optical-imaging modalities with high temporal resolution and spatial precision, we aim to bridge the gap between molecules and cells, either as independent entities in culture, as components of organoids, or as constituents of living tissues. The richness and magnitude of the big-data obtained over periods ranging from seconds to hours create new challenges for obtaining quantitative representations of the observed dynamics and for deriving accurate and comprehensive models for the underlying developmental mechanisms. With these type of dynamic studies we expect to integrate molecular snapshots obtained at molecular and atomic resolution using cryoEM with live-cell processes, in an effort to generate ‘molecular movies' allowing us to obtain frameworks for analyzing some of the molecular contacts and switches that participate in the regulation, availability, and intracellular traffic of the many molecules involved in signal transduction, immune responsiveness, lipid homeostasis, cell-cell recognition and organelle biogenesis. Such biological phenomena have importance for our understanding of many diseases including cancer, viral infection and pathogen invasion, Alzheimer's, as well as other neurological diseases.

Harvard Medical School

Dept. of Cell Biology, WAB-133

200 Longwood Avenue

Boston, MA 02115

Lab telephone: 617-713-8888

Lab fax: 617-713-8898

Possible role of deep tubular invaginations of the plasma membrane in MHC-I trafficking.
Authors: Authors: Massol RH, Larsen JE, Kirchhausen T.
Exp Cell Res
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Endocytosis is not required for the selective lipid uptake mediated by murine SR-BI.
Authors: Authors: Nieland TJ, Ehrlich M, Krieger M, Kirchhausen T.
Biochim Biophys Acta
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The transcription factor NFAT3 mediates neuronal survival.
Authors: Authors: Benedito AB, Lehtinen M, Massol R, Lopes UG, Kirchhausen T, Rao A, Bonni A.
J Biol Chem
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Single-molecule live-cell imaging of clathrin-based endocytosis.
Authors: Authors: Kirchhausen T, Boll W, van Oijen A, Ehrlich M.
Biochem Soc Symp
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Structure of an auxilin-bound clathrin coat and its implications for the mechanism of uncoating.
Authors: Authors: Fotin A, Cheng Y, Grigorieff N, Walz T, Harrison SC, Kirchhausen T.
Nature
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Molecular model for a complete clathrin lattice from electron cryomicroscopy.
Authors: Authors: Fotin A, Cheng Y, Sliz P, Grigorieff N, Harrison SC, Kirchhausen T, Walz T.
Nature
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Crystal structure of the clathrin adaptor protein 1 core.
Authors: Authors: Heldwein EE, Macia E, Wang J, Yin HL, Kirchhausen T, Harrison SC.
Proc Natl Acad Sci U S A
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Endocytosis by random initiation and stabilization of clathrin-coated pits.
Authors: Authors: Ehrlich M, Boll W, Van Oijen A, Hariharan R, Chandran K, Nibert ML, Kirchhausen T.
Cell
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The small chemical vacuolin-1 inhibits Ca(2+)-dependent lysosomal exocytosis but not cell resealing.
Authors: Authors: Cerny J, Feng Y, Yu A, Miyake K, Borgonovo B, Klumperman J, Meldolesi J, McNeil PL, Kirchhausen T.
EMBO Rep
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Cholera toxin toxicity does not require functional Arf6- and dynamin-dependent endocytic pathways.
Authors: Authors: Massol RH, Larsen JE, Fujinaga Y, Lencer WI, Kirchhausen T.
Mol Biol Cell
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