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

Cell biology: balancing act.
Authors: Authors: Ordureau A, Harper JW.
Nature
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Quantitative proteomics identifies NCOA4 as the cargo receptor mediating ferritinophagy.
Authors: Authors: <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1244106">Mancias JD</a>, Wang X, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1242109">Gygi SP</a>, Harper JW, Kimmelman AC.
Nature
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TIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complex.
Authors: Authors: Guarani V, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231877">Paulo J</a>, Zhai B, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1243594">Huttlin EL</a>, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1242109">Gygi SP</a>, Harper JW.
Mol Cell Biol
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Spindle assembly factor protection.
Authors: Authors: Vaites LL, Harper JW.
Mol Cell
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The seven wonders of ubiquitin: a multi-interview: Personal insights into the ubiquitin field. Interview by Nonia Pariente.
Authors: Authors: Dikic I, Harper W, Hay R, Langer T, Rape M, Sixma T, Walczak H.
EMBO Rep
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Building and remodelling Cullin-RING E3 ubiquitin ligases.
Authors: Authors: Lydeard JR, Schulman BA, Harper JW.

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A novel Hap1-Tsc1 interaction regulates neuronal mTORC1 signaling and morphogenesis in the brain.
Authors: Authors: Mejia LA, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1237651">Litterman N</a>, Ikeuchi Y, de la Torre-Ubieta L, Bennett EJ, Zhang C, Harper JW, Bonni A.
J Neurosci
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The histone demethylase LSD1/KDM1A promotes the DNA damage response.
Authors: Authors: Mosammaparast N, Kim H, Laurent B, Zhao Y, Lim HJ, Majid MC, Dango S, Luo Y, Hempel K, Sowa ME, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1242109">Gygi SP</a>, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1246152">Steen H</a>, Harper JW, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1249530">Yankner B</a>, Shi Y.
J Cell Biol
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Parallel SCF adaptor capture proteomics reveals a role for SCFFBXL17 in NRF2 activation via BACH1 repressor turnover.
Authors: Authors: Tan MK, Lim HJ, Bennett EJ, Shi Y, Harper JW.
Mol Cell
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Increased body mass index is associated with earlier time to loss of response to infliximab in patients with inflammatory bowel disease.
Authors: Authors: Harper JW, Sinanan MN, Zisman TL.
Inflamm Bowel Dis
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