La investigación de Diane S. Lidke se centra en la aplicación de microscopía de fluorescencia y técnicas biofísicas al estudio de la transducción de señales celulares. El tema del trabajo del Dr. Lidke es visualizar y cuantificar la dinámica de las proteínas que regulan la señalización celular, tanto en estado normal como enfermo. El objetivo final es identificar los mecanismos moleculares que alteran la señalización en el cáncer y la respuesta inmune.
Research in the Lidke Laboratory integrates the disciplines of biophysics, bio-imaging and quantitative biology to gain new and fundamental understanding of the components and dynamics of cell signaling pathways. This involves the measurement of protein behavior in living cells to capture and quantify biochemical events that initiate signaling. The focus is on the study of the receptor tyrosine kinases and immunoreceptors, and how these are altered in disease or influenced by therapeutics.
Diane Lidke, Ph.D.
Professor & Vice-Chair for Research, Department of Pathology
Lidke recibió su licenciatura en Física en 1994. Obtuvo su doctorado en Ciencias Biofísicas y Física Médica de la Universidad de Minnesota en 2002. Su investigación postdoctoral fue en el laboratorio de Thomas Jovin en el Instituto Max Planck de Química Biofísica en Goettingen, Alemania. . Se unió al Departamento de Patología de la UNM en 2005.
N.L. Andrews, J.R. Pfeiffer, A.M. Martinez, D.M. Haaland, R.W. Davis, T. Kawakami, J.M. Oliver, B.S. Wilson and D.S. Lidke. Small, mobile FcRI aggregates are signaling competent. Immunity, 31: 469-479 (2009) PMC2828771
S.T. Low-Nam, K.A. Lidke, P.J. Cutler, R.C. Roovers, P.M.P. van Bergen en Henegouwen, B.S. Wilson, D.S. Lidke. ErbB1 dimerization is promoted by domain co-confinement and stabilized by ligand. Nature Structural & Molecular Biology, 18: 1244-1249 (2011) PMC3210321
S.L. Schwartz, C. Cleyrat, M. Olah, P. Relich, G. Phillips, W.S. Hlavacek, K.A. Lidke, B.S. Wilson and D.S. Lidke. Differential mast cell outcomes are sensitive to FcRI-Syk binding kinetics. Molecular Biology of the Cell - Quantitative Biology Special Issue 28: 3397-3414 (2017) PMC5687039**MBoC Highlight article
A.M. Brandsma*, S.L. Schwartz*, C.C. Valley, G.L.A. Blezer, G. Vidarsson, K.A. Lidke, T. ten Broeke, D.S. Lidke^, J.H.W. Leusen^. Mechanisms of inside-out signaling of the high affinity IgG-receptor FcRI. Science Signaling. 11: eaaq0891 (2018) PMID: 30042128 ^Lidke and Leusen are co-corresponding authors.
E. Salazar-Cavazos, C. Franco Nitta, E.D. Mitra, B.S. Wilson, K.A. Lidke, W.S. Hlavacek, Lidke, D.S. Multisite EGFR phosphorylation is regulated by adaptor protein abundances and dimer lifetimes. Molecular Biology of the Cell, 19:695-708 (2020) PMC7202077
Research in the Lidke Laboratory integrates the disciplines of biophysics, bio-imaging and quantitative biology to gain new and fundamental understanding of the components and dynamics of cell signaling pathways. This involves the measurement of protein behavior in living cells to capture and quantify biochemical events that initiate signaling. The focus is on the study of the receptor tyrosine kinases and immunoreceptors, and how these are altered in disease or influenced by therapeutics.
Diane Lidke, Ph.D.
Professor & Vice-Chair for Research, Department of Pathology
Lidke recibió su licenciatura en Física en 1994. Obtuvo su doctorado en Ciencias Biofísicas y Física Médica de la Universidad de Minnesota en 2002. Su investigación postdoctoral fue en el laboratorio de Thomas Jovin en el Instituto Max Planck de Química Biofísica en Goettingen, Alemania. . Se unió al Departamento de Patología de la UNM en 2005.
N.L. Andrews, J.R. Pfeiffer, A.M. Martinez, D.M. Haaland, R.W. Davis, T. Kawakami, J.M. Oliver, B.S. Wilson and D.S. Lidke. Small, mobile FcRI aggregates are signaling competent. Immunity, 31: 469-479 (2009) PMC2828771
S.T. Low-Nam, K.A. Lidke, P.J. Cutler, R.C. Roovers, P.M.P. van Bergen en Henegouwen, B.S. Wilson, D.S. Lidke. ErbB1 dimerization is promoted by domain co-confinement and stabilized by ligand. Nature Structural & Molecular Biology, 18: 1244-1249 (2011) PMC3210321
S.L. Schwartz, C. Cleyrat, M. Olah, P. Relich, G. Phillips, W.S. Hlavacek, K.A. Lidke, B.S. Wilson and D.S. Lidke. Differential mast cell outcomes are sensitive to FcRI-Syk binding kinetics. Molecular Biology of the Cell - Quantitative Biology Special Issue 28: 3397-3414 (2017) PMC5687039**MBoC Highlight article
A.M. Brandsma*, S.L. Schwartz*, C.C. Valley, G.L.A. Blezer, G. Vidarsson, K.A. Lidke, T. ten Broeke, D.S. Lidke^, J.H.W. Leusen^. Mechanisms of inside-out signaling of the high affinity IgG-receptor FcRI. Science Signaling. 11: eaaq0891 (2018) PMID: 30042128 ^Lidke and Leusen are co-corresponding authors.
E. Salazar-Cavazos, C. Franco Nitta, E.D. Mitra, B.S. Wilson, K.A. Lidke, W.S. Hlavacek, Lidke, D.S. Multisite EGFR phosphorylation is regulated by adaptor protein abundances and dimer lifetimes. Molecular Biology of the Cell, 19:695-708 (2020) PMC7202077
Diane S. Lidke. Doctor.
Departamento de patología
Centro de investigación del cáncer, sala 203
Escuela de Medicina de la Universidad de Nuevo México
Albuquerque, Nuevo México 87131