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

Cdc42 is required for PIP(2)-induced actin polymerization and early development but not for cell viability.
Authors: Authors: Chen F, Ma L, Parrini MC, Mao X, Lopez M, Wu C, Marks PW, Davidson L, Kwiatkowski DJ, Kirchhausen T, Orkin SH, Rosen FS, Mayer BJ, Kirschner MW, Alt FW.
Curr Biol
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Multivalent binding of nonnative substrate proteins by the chaperonin GroEL.
Authors: Authors: Farr GW, Furtak K, Rowland MB, Ranson NA, Saibil HR, Kirchhausen T, Horwich AL.
Cell
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Peptide-in-groove interactions link target proteins to the beta-propeller of clathrin.
Authors: Authors: ter Haar E, Harrison SC, Kirchhausen T.
Proc Natl Acad Sci U S A
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Clathrin.
Authors: Authors: Kirchhausen T.
Annu Rev Biochem
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Studies on the inhibition of endosome fusion by GTPgammaS-bound ARF.
Authors: Authors: Jones AT, Spiro DJ, Kirchhausen T, Melançon P, Wessling-Resnick M.
J Cell Sci
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Cytolytic T lymphocyte-associated antigen-4 and the TCR zeta/CD3 complex, but not CD28, interact with clathrin adaptor complexes AP-1 and AP-2.
Authors: Authors: Schneider H, Martin M, Agarraberes FA, Yin L, Rapoport I, Kirchhausen T, Rudd CE.
J Immunol
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Functional organization of clathrin in coats: combining electron cryomicroscopy and X-ray crystallography.
Authors: Authors: Musacchio A, Smith CJ, Roseman AM, Harrison SC, Kirchhausen T, Pearse BM.
Mol Cell
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The interaction between N-WASP and the Arp2/3 complex links Cdc42-dependent signals to actin assembly.
Authors: Authors: Rohatgi R, Ma L, Miki H, Lopez M, Kirchhausen T, Takenawa T, Kirschner MW.
Cell
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Cell biology. Boa constrictor or rattlesnake?
Authors: Authors: Kirchhausen T.
Nature
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Adaptors for clathrin-mediated traffic.
Authors: Authors: Kirchhausen T.
Annu Rev Cell Dev Biol
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