Stephen Blacklow

Stephen Blacklow, MD, PhD

Gustavus Adolphus Pfeiffer Professor of Biological Chemistry and Molecular Pharmacology, Harvard Medical School

Dr. Blacklow is currently the Gustavus Adolphus Pfeiffer Professor and Chair of the Department of Biological Chemistry and Molecular Pharmacology at Harvard Medical School, and a member of the Department of Cancer Biology at the Dana Farber Cancer Institute.

Research led by Dr. Blacklow’s team has shown how cell surface receptors can convey a developmental signal directly from one contacting cell surface to the next and then from the membrane to the nucleus. He has elucidated key molecular events in Notch signal transduction, a conserved cell-cell communication system that influences cell fate decisions in all metazoan organisms, and that is frequently hijacked as an oncogenic driver in human leukemia. His research on the Notch pathway has led to the development of new investigational therapies for hematologic malignancies such as T cell acute lymphocytic leukemia (ALL).

Dr. Blacklow was a recipient of the National Cancer Institute’s prestigious Outstanding Investigator Award in 2017, and elected to the Association of American Physicians in 2018. Dr. Blacklow directed the MD-PhD Program in Basic and Translational Sciences at Harvard Medical School and has served on Advisory Committees for pre-clinical departments, graduate programs, and MD-PhD programs at several major research universities and institutions, including Stanford, the University of Pennsylvania, and the Memorial Sloan Kettering Cancer Center.

Dr. Blacklow received his MD and PhD degrees from Harvard University in 1991, completed his residency in Clinical Pathology at Brigham and Women’s Hospital, and carried out postdoctoral research at the Whitehead Institute with Dr. Peter S. Kim.

A Spatiotemporal Map of Co-Receptor Signaling Networks Underlying B Cell Activation
Authors: Authors: Katherine J Susa , Gary A Bradshaw, Robyn J Eisert, Charlotte M Schilling, Marian Kalocsay, Stephen C Blacklow, Andrew C Kruse
CellPress
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Tetraspanins: structure, dynamics, and principles of partner-protein recognition
Authors: Authors: Katherine J. Susa, Andrew C. Kruse, and Stephen C. Blacklow
CellPress
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Dual Allosteric Inhibition of SHP2 Phosphatase.
Authors: Authors: Fodor M, Price E, Wang P, Lu H, Argintaru A, Chen Z, Glick M, Hao HX, Kato M, Koenig R, LaRochelle JR, Liu G, McNeill E, Majumdar D, Nishiguchi GA, Perez LB, Paris G, Quinn CM, Ramsey T, Sendzik M, Shultz MD, Williams SL, Stams T, Blacklow SC, Acker MG, LaMarche MJ.
ACS Chem Biol
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Structure and function of the Mind bomb E3 ligase in the context of Notch signal transduction.
Authors: Authors: Guo B, McMillan BJ, Blacklow SC.
Curr Opin Struct Biol
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Intrinsic selectivity of Notch 1 for Delta-like 4 over Delta-like 1.
Authors: Authors: Andrawes MB, Xu X, Liu H, Ficarro SB, Marto JA, Aster JC, Blacklow SC.
J Biol Chem
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Notch dimerization is required for leukemogenesis and T-cell development.
Authors: Authors: Liu H, Chi AW, Arnett KL, Chiang MY, Xu L, Shestova O, Wang H, Li YM, Bhandoola A, Aster JC, Blacklow SC, Pear WS.
Genes Dev
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Notch directly regulates Gata3 expression during T helper 2 cell differentiation.
Authors: Authors: Fang TC, Yashiro-Ohtani Y, Del Bianco C, Knoblock DM, Blacklow SC, Pear WS.
Immunity
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Notch subunit heterodimerization and prevention of ligand-independent proteolytic activation depend, respectively, on a novel domain and the LNR repeats.
Authors: Authors: Sanchez-Irizarry C, Carpenter AC, Weng AP, Pear WS, Aster JC, Blacklow SC.
Mol Cell Biol
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An intramolecular spin of the LDL receptor beta propeller.
Authors: Authors: Jeon H, Blacklow SC.
Structure
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The folding and structural integrity of the first LIN-12 module of human Notch1 are calcium-dependent.
Authors: Authors: Aster JC, Simms WB, Zavala-Ruiz Z, Patriub V, North CL, Blacklow SC.
Biochemistry
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