Tom Rapoport

Tom Rapoport, Ph.D.

Don W. Fawcett Professor of Cell Biology (HMS)
HHMI Investigator
LHRRB 401

Tom Rapoport, Ph.D., joined the faculty at Harvard Medical School in 1995. He received his Ph.D. in Biochemistry from the Humboldt University in East-Berlin for work in enzymology. He then focused on mathematical modeling of metabolism, for which he received his second degree (Habilitation) from the same institution. Before moving to the US, he worked at the Central Institute of Molecular Biology of the Academy of Sciences of the GDR and later at the Max-Delbrueck Center for Molecular Medicine in Berlin-Buch. In 1997, he became a Howard Hughes Medical Institute Investigator.

The Rapoport Lab is interested in the mechanisms by which proteins are transported across membranes, how misfolded proteins are degraded, and how organelles form and maintain their characteristic shapes. Most of the projects center around the endoplasmic reticulum (ER). One project concerns the molecular mechanism by which proteins are translocated across the ER membrane or across the plasma membrane in bacteria and archaea. Much of the current work deals with ERAD (ER-associated protein degradation), a process in which misfolded proteins are retro-translocated across the ER membrane into the cytosol. Major questions concern the mechanism by which proteins move across the membrane and are extracted by the Cdc48 ATPase. Another project concerns the mechanism by which ER morphology, specifically the tubular ER network, is generated. More recently, the Rapoport lab has started to study how proteins are imported into peroxisomes, and how lung surfactant proteins generate lamellar bodies. The lab employs a variety of different techniques, including biochemical methods, such as reconstitutions with purified proteins, and structural biology methods, including X-ray crystallography and cryo-electron microscopy.

Harvard Medical School

Dept. of Cell Biology, LHRRB 401

240 Longwood Avenue

Boston, MA 02115

Lab phone: 617-432-1612

Dissociation of the dimeric SecA ATPase during protein translocation across the bacterial membrane.
Authors: Authors: Or E, Navon A, Rapoport T.
EMBO J
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A novel centrosome-associated protein with affinity for microtubules.
Authors: Authors: Stein PA, Toret CP, Salic AN, Rolls MM, Rapoport TA.
J Cell Sci
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Three-dimensional structure of the bacterial protein-translocation complex SecYEG.
Authors: Authors: Breyton C, Haase W, Rapoport TA, Kühlbrandt W, Collinson I.
Nature
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Profile: Tom Rapoport interviewed by Rabiya S. Tuma.
Authors: Authors: Rapoport T.
Trends Cell Biol
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Mathematical models of protein kinase signal transduction.
Authors: Authors: Heinrich R, Neel BG, Rapoport TA.
Mol Cell
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Targeting of rough endoplasmic reticulum membrane proteins and ribosomes in invertebrate neurons.
Authors: Authors: Rolls MM, Hall DH, Victor M, Stelzer EH, Rapoport TA.
Mol Biol Cell
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Retro-translocation of proteins from the endoplasmic reticulum into the cytosol.
Authors: Authors: Tsai B, Ye Y, Rapoport TA.
Nat Rev Mol Cell Biol
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The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol.
Authors: Authors: Ye Y, Meyer HH, Rapoport TA.
Nature
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Protein folding taking shape. Workshop on molecular chaperones.
Authors: Authors: Horwich AL, Fenton WA, Rapoport TA.
EMBO Rep
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Kinesin carries the signal.
Authors: Authors: Verhey KJ, Rapoport TA.
Trends Biochem Sci
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