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

Direct interaction of the Wiskott-Aldrich syndrome protein with the GTPase Cdc42.
Authors: Authors: Kolluri R, Tolias KF, Carpenter CL, Rosen FS, Kirchhausen T.
Proc Natl Acad Sci U S A
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Wortmannin alters the transferrin receptor endocytic pathway in vivo and in vitro.
Authors: Authors: Spiro DJ, Boll W, Kirchhausen T, Wessling-Resnick M.
Mol Biol Cell
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A clathrin-binding site in the hinge of the beta 2 chain of mammalian AP-2 complexes.
Authors: Authors: Shih W, Gallusser A, Kirchhausen T.
J Biol Chem
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Role of the regulatory domain of the EGF-receptor cytoplasmic tail in selective binding of the clathrin-associated complex AP-2.
Authors: Authors: Boll W, Gallusser A, Kirchhausen T.
Curr Biol
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Interaction of tyrosine-based sorting signals with clathrin-associated proteins.
Authors: Authors: Ohno H, Stewart J, Fournier MC, Bosshart H, Rhee I, Miyatake S, Saito T, Gallusser A, Kirchhausen T, Bonifacino JS.
Science
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Saccharomyces cerevisiae Apl2p, a homologue of the mammalian clathrin AP beta subunit, plays a role in clathrin-dependent Golgi functions.
Authors: Authors: Rad MR, Phan HL, Kirchrath L, Tan PK, Kirchhausen T, Hollenberg CP, Payne GS.
J Cell Sci
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Molecular characterization of an apical early endosomal glycoprotein from developing rat intestinal epithelial cells.
Authors: Authors: Speelman BA, Allen K, Grounds TL, Neutra MR, Kirchhausen T, Wilson JM.
J Biol Chem
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Stoichiometric interaction of the epidermal growth factor receptor with the clathrin-associated protein complex AP-2.
Authors: Authors: Sorkin A, McKinsey T, Shih W, Kirchhausen T, Carpenter G.
J Biol Chem
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A late Golgi sorting function for Saccharomyces cerevisiae Apm1p, but not for Apm2p, a second yeast clathrin AP medium chain-related protein.
Authors: Authors: Stepp JD, Pellicena-Palle A, Hamilton S, Kirchhausen T, Lemmon SK.
Mol Biol Cell
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A rab protein is required for the assembly of SNARE complexes in the docking of transport vesicles.
Authors: Authors: Søgaard M, Tani K, Ye RR, Geromanos S, Tempst P, Kirchhausen T, Rothman JE, Söllner T.
Cell
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