Wade Harper, Ph.D.

Wade Harper, Ph.D.

Bert and Natalie Vallee Professor of Molecular Pathology (HMS)
Professor of Cell Biology (HMS)
Chair of the Department of Cell Biology (HMS)

Wade Harper, Ph.D., is the B and N Vallee Professor of Molecular Pathology, a Professor of Cell Biology, and the Chair of Cell Biology in the Blavatnik Institute at Harvard Medical School. He received his Ph.D. in Chemistry from Georgia Institute of Technology, prior to performing post-doctoral work in protein biochemistry of growth factors at Harvard Medical School. He joined the faculty in the Department of Biochemistry and Molecular Biology at Baylor College of Medicine in 1988 and subsequently moved to the Department of Pathology at Harvard Medical School (in 2003) and to the Department of Cell Biology in 2011.

The Harper Lab studies mechanisms underlying cellular homeostasis and signaling, with a focus on the ubiquitin system and the autophagy-lysosome system. The interest in the ubiquitin-proteasome system in the Harper Lab initially emerged through studies to understand how cell cycle regulators (cyclins and CDK inhibitors) are degraded to control cell cycle transitions, resulting in the discovery of cullin-RING ubiquitin ligases, and their roles in phosphorylation-dependent protein degradation. The Harper Lab currently uses quantitative proteomics, imaging, and biochemical approaches to elucidate underlying biochemical mechanisms controlling protein turnover, and applies these approaches to examine regulatory pathways relevant to various neurodegenerative disease, including Parkinson’s and Alzheimer’s diseases. A major focus currently is the PARKIN ubiquitin ligase, which controls turnover of damaged mitochondria via the autophagy pathway and is mutated in Parkinson’s Disease. The Harper Lab, together with the Gygi Lab at HMS, is also using proteomics to develop a large-scale human protein interaction network including the majority of proteins encoded by the human genome.

Harvard Medical School

Dept. of Cell Biology, C-462A

240 Longwood Avenue

Boston, MA 02115

Lab telephone: 617-432-6590

Two Distinct Types of E3 Ligases Work in Unison to Regulate Substrate Ubiquitylation.
Authors: Authors: Scott DC, Rhee DY, Duda DM, Kelsall IR, Olszewski JL, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231877">Paulo JA</a>, de Jong A, Ovaa H, Alpi AF, Harper JW, Schulman BA.
Cell
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Endosome-ER Contacts Control Actin Nucleation and Retromer Function through VAP-Dependent Regulation of PI4P.
Authors: Authors: Dong R, Saheki Y, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/32571414">Swarup S</a>, Lucast L, Harper JW, De Camilli P.
Cell
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Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation.
Authors: Authors: Münch C, Harper JW.
Nature
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A protein interaction map for cell-cell adhesion regulators identifies DUSP23 as a novel phosphatase for ß-catenin.
Authors: Authors: Gallegos LL, Ng MR, Sowa ME, Selfors LM, White A, Zervantonakis IK, Singh P, Dhakal S, Harper JW, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1233899">Brugge JS</a>.
Sci Rep
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Dual RING E3 Architectures Regulate Multiubiquitination and Ubiquitin Chain Elongation by APC/C.
Authors: Authors: Brown NG, VanderLinden R, Watson ER, Weissmann F, Ordureau A, Wu KP, Zhang W, Yu S, Mercredi PY, Harrison JS, Davidson IF, Qiao R, Lu Y, Dube P, Brunner MR, Grace CRR, Miller DJ, Haselbach D, Jarvis MA, Yamaguchi M, Yanishevski D, Petzold G, Sidhu SS, Kuhlman B, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231883">Kirschner MW</a>, Harper JW, Peters JM, Stark H, Schulman BA.
Cell
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System-Wide Modulation of HECT E3 Ligases with Selective Ubiquitin Variant Probes.
Authors: Authors: Zhang W, Wu KP, Sartori MA, Kamadurai HB, Ordureau A, Jiang C, Mercredi PY, Murchie R, Hu J, Persaud A, Mukherjee M, Li N, Doye A, Walker JR, Sheng Y, Hao Z, Li Y, Brown KR, Lemichez E, Chen J, Tong Y, Harper JW, Moffat J, Rotin D, Schulman BA, Sidhu SS.
Mol Cell
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The CASTOR Proteins Are Arginine Sensors for the mTORC1 Pathway.
Authors: Authors: Chantranupong L, Scaria SM, Saxton RA, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1250755">Gygi MP</a>, Shen K, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/116074521">Wyant GA</a>, Wang T, Harper JW, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1242109">Gygi SP</a>, Sabatini DM.
Cell
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Cytokinesis involves a nontranscriptional function of the Hippo pathway effector YAP.
Authors: Authors: Bui DA, Lee W, White AE, Harper JW, Schackmann RC, Overholtzer M, Selfors LM, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1233899">Brugge JS</a>.
Sci Signal
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Corrigendum: Systematic proteomics of the VCP-UBXD adaptor network identifies a role for UBXN10 in regulating ciliogenesis.
Authors: Authors: Raman M, Sergeev M, Garnaas M, Lydeard JR, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1243594">Huttlin EL</a>, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1237905">Goessling W</a>, Shah JV, Harper JW.
Nat Cell Biol
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The MAP kinase pathway coordinates crossover designation with disassembly of synaptonemal complex proteins during meiosis.
Authors: Authors: <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1230673">Nadarajan S</a>, Mohideen F, Tzur YB, Ferrandiz N, Crawley O, Montoya A, Faull P, Snijders AP, Cutillas PR, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1253633">Jambhekar A</a>, Blower MD, Martinez-Perez E, Harper JW, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1257301">Colaiacovo MP</a>.
Elife
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