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

Constriction and Dnm1p recruitment are distinct processes in mitochondrial fission.
Authors: Authors: Legesse-Miller A, Massol RH, Kirchhausen T.
Mol Biol Cell
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Discovery of chemical inhibitors of the selective transfer of lipids mediated by the HDL receptor SR-BI.
Authors: Authors: Nieland TJ, Penman M, Dori L, Krieger M, Kirchhausen T.
Proc Natl Acad Sci U S A
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T-cell engagement of dendritic cells rapidly rearranges MHC class II transport.
Authors: Authors: Boes M, Cerny J, Massol R, Op den Brouw M, Kirchhausen T, Chen J, Ploegh HL.
Nature
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The mu2 subunit of the clathrin adaptor AP-2 binds to FDNPVY and YppØ sorting signals at distinct sites.
Authors: Authors: Boll W, Rapoport I, Brunner C, Modis Y, Prehn S, Kirchhausen T.
Traffic
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L1 endocytosis is controlled by a phosphorylation-dephosphorylation cycle stimulated by outside-in signaling by L1.
Authors: Authors: Schaefer AW, Kamei Y, Kamiguchi H, Wong EV, Rapoport I, Kirchhausen T, Beach CM, Landreth G, Lemmon SK, Lemmon V.
J Cell Biol
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Clathrin adaptors really adapt.
Authors: Authors: Kirchhausen T.
Cell
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Single-handed recognition of a sorting traffic motif by the GGA proteins.
Authors: Authors: Kirchhausen T.
Nat Struct Biol
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Structure of the Sec23p/24p and Sec13p/31p complexes of COPII.
Authors: Authors: Lederkremer GZ, Cheng Y, Petre BM, Vogan E, Springer S, Schekman R, Walz T, Kirchhausen T.
Proc Natl Acad Sci U S A
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Use of biomimetic diversity-oriented synthesis to discover galanthamine-like molecules with biological properties beyond those of the natural product.
Authors: Authors: Pelish HE, Westwood NJ, Feng Y, Kirchhausen T, Shair MD.
J Am Chem Soc
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Three ways to make a vesicle.
Authors: Authors: Kirchhausen T.
Nat Rev Mol Cell Biol
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