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

Lab fax: 617-432-6591

NCOA4 maintains murine erythropoiesis via cell autonomous and non-autonomous mechanisms.
Authors: Authors: Santana-Codina N, Gableske S, Quiles del Rey M, Malachowska B, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1250277">Jedrychowski MP</a>, Biancur DE, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1235921">Schmidt PJ</a>, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1245794">Fleming MD</a>, Fendler W, Harper JW, Kimmelman AC, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1244106">Mancias JD</a>.
Haematologica
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TEX264 Is an Endoplasmic Reticulum-Resident ATG8-Interacting Protein Critical for ER Remodeling during Nutrient Stress.
Authors: Authors: An H, Ordureau A, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231877">Paulo JA</a>, Shoemaker CJ, Denic V, Harper JW.
Mol Cell
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Probing the Global Cellular Responses to Lipotoxicity Caused by Saturated Fatty Acids.
Authors: Authors: Piccolis M, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/123145867">Bond LM</a>, Kampmann M, Pulimeno P, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/77445740">Chitraju C</a>, Jayson CBK, Vaites LP, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/123145846">Boland S</a>, Lai ZW, Gabriel KR, Elliott SD, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231877">Paulo JA</a>, Harper JW, Weissman JS, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/29624596">Walther TC</a>, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/29624598">Farese RV</a>.
Mol Cell
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Excessive Cell Growth Causes Cytoplasm Dilution And Contributes to Senescence.
Authors: Authors: Neurohr GE, Terry RL, Lengefeld J, Bonney M, Brittingham GP, Moretto F, Miettinen TP, Vaites LP, Soares LM, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231877">Paulo JA</a>, Harper JW, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1234590">Buratowski S</a>, Manalis S, van Werven FJ, Holt LJ, Amon A.
Cell
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Mitotic regulators TPX2 and Aurora A protect DNA forks during replication stress by counteracting 53BP1 function.
Authors: Authors: Byrum AK, Carvajal-Maldonado D, Mudge MC, Valle-Garcia D, Majid MC, Patel R, Sowa ME, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1242109">Gygi SP</a>, Harper JW, Shi Y, Vindigni A, Mosammaparast N.
J Cell Biol
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Angelman syndrome-associated point mutations in the Zn2+-binding N-terminal (AZUL) domain of UBE3A ubiquitin ligase inhibit binding to the proteasome.
Authors: Authors: Kühnle S, Martínez-Noël G, Leclere F, Hayes SD, Harper JW, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1237682">Howley PM</a>.
J Biol Chem
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RAB7A phosphorylation by TBK1 promotes mitophagy via the PINK-PARKIN pathway.
Authors: Authors: Heo JM, Ordureau A, Swarup S, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231877">Paulo JA</a>, Shen K, Sabatini DM, Harper JW.
Sci Adv
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Dynamics of PARKIN-Dependent Mitochondrial Ubiquitylation in Induced Neurons and Model Systems Revealed by Digital Snapshot Proteomics.
Authors: Authors: Ordureau A, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1231877">Paulo JA</a>, Zhang W, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1230786">Ahfeldt T</a>, Zhang J, Cohn EF, Hou Z, Heo JM, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1230753">Rubin LL</a>, Sidhu SS, <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1242109">Gygi SP</a>, Harper JW.
Mol Cell
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Protein aggregates caught stalling.
Authors: Authors: <a href="https://connects.catalyst.harvard.edu/Profiles/profile/1258221">Pontano Vaites L</a>, Harper JW.
Nature
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Systematic analysis of ribophagy in human cells reveals bystander flux during selective autophagy.
Authors: Authors: An H, Harper JW.
Nat Cell Biol
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