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

Inhibition of dynamin completely blocks compensatory synaptic vesicle endocytosis.
Authors: Authors: Newton AJ, Kirchhausen T, Murthy VN.
Proc Natl Acad Sci U S A
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Macropinocytosis: regulated coordination of endocytic and exocytic membrane traffic events.
Authors: Authors: Falcone S, Cocucci E, Podini P, Kirchhausen T, Clementi E, Meldolesi J.
J Cell Sci
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A burst of auxilin recruitment determines the onset of clathrin-coated vesicle uncoating.
Authors: Authors: Massol RH, Boll W, Griffin AM, Kirchhausen T.
Proc Natl Acad Sci U S A
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The Cdc42 inhibitor secramine B prevents cAMP-induced K+ conductance in intestinal epithelial cells.
Authors: Authors: Pelish HE, Ciesla W, Tanaka N, Reddy K, Shair MD, Kirchhausen T, Lencer WI.
Biochem Pharmacol
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Dynasore, a cell-permeable inhibitor of dynamin.
Authors: Authors: Macia E, Ehrlich M, Massol R, Boucrot E, Brunner C, Kirchhausen T.
Dev Cell
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Synthesis of a 10,000-membered library of molecules resembling carpanone and discovery of vesicular traffic inhibitors.
Authors: Authors: Goess BC, Hannoush RN, Chan LK, Kirchhausen T, Shair MD.
J Am Chem Soc
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Secramine inhibits Cdc42-dependent functions in cells and Cdc42 activation in vitro.
Authors: Authors: Pelish HE, Peterson JR, Salvarezza SB, Rodriguez-Boulan E, Chen JL, Stamnes M, Macia E, Feng Y, Shair MD, Kirchhausen T.
Nat Chem Biol
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Perforin triggers a plasma membrane-repair response that facilitates CTL induction of apoptosis.
Authors: Authors: Keefe D, Shi L, Feske S, Massol R, Navarro F, Kirchhausen T, Lieberman J.
Immunity
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The small G-protein Arf6GTP recruits the AP-2 adaptor complex to membranes.
Authors: Authors: Paleotti O, Macia E, Luton F, Klein S, Partisani M, Chardin P, Kirchhausen T, Franco M.
J Biol Chem
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An emergency response team for membrane repair.
Authors: Authors: McNeil PL, Kirchhausen T.
Nat Rev Mol Cell Biol
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