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Research Focus
Molecular cell bioengineering: the application of
engineering approaches to develop quantitative understanding of
cell function in terms of fundamental molecular properties, and
to apply this understanding for improved design of cell-based technologies.
Our group focuses on elucidating important aspects of receptor-mediated
regulation of mammalian blood and tissue cell behavioral functions
such as proliferation, adhesion, migration, and macromolecular transport.
A central paradigm of our work is development and testing of mechanistic
models-- based on principles from engineering analysis and synthesis
-- for receptor regulation of cell function by exploiting techniques
of molecular biology to alter parameters characterizing receptor
or ligand properties in well-characterized cell systems. Quantitative
experimental assays are used to measure cell function and receptor/ligand
interaction parameters. Problems are motivated by health care technologies
of interest to pharmaceutical and biotechnological companies.
Selected Publications
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for a complete list of publications.
152. Sarkar, C.A., K. Lowenhaupt, T. Horan, T.C. Boone, B. Tidor,
and D.A. Lauffenburger, “Rational Cytokine Design for Increased
Lifetime and Enhanced Potency Using pH-Activated ‘Histidine
Switching’”, Nature Biotech. 20: 908-913 (2002).
153. Dewitt, A., T. Iida, H.-Y. Lam, V. Hill, H.S. Wiley, and D.A.
Lauffenburger, “Affinity Regulates Spatial Range of EGF Receptor
Autocrine Ligands”, Develop. Biol. 250: 305-316 (2002).
154. Sarkar, C.A. and D.A. Lauffenburger, “Cell-Level Pharmacokinetic
Model of GCSF: Implications for Ligand Lifetime and Potency in Vivo”,
Molec. Pharmacol. 63: 147-158 (2003).
155. Hendriks, B., L.K. Opresko, H.S. Wiley, and D.A. Lauffenburger,
“Co-Regulation of EGFR/HER2 Levels and Locations: Quantitative
Analysis of HER2 Overexpression Effects”, Cancer Res. 63:
1130-1137 (2003).
156. Ricci, M.S., C.A. Sarkar, E.M. Fallon, D.A. Lauffenburger,
and D.N. Brems, “pH Dependence of Structural Stability of
IL-2 and GCSF”, Protein Sci. 12: 1030-1038 (2003).
155. Sarkar, C.A., Lowenhaupt, K., Wang, P.J., Horan, T., and D.A.
Lauffenburger, “Parsing the Effects of Binding, Signaling,
and Trafficking on the Mitogenic Potency of GCSF Analogs”,
Biotech. Progr. 19: 955-964 (2003).
156. Hendriks, B., L.K. Opresko, H.S. Wiley, and D.A. Lauffenburger,
“Quantitative Analysis of HER2-Mediated Effects on HER2 and
EGFR Endocytosis: Distribution of Homo- and Hetero-dimers Depends
on Relative HER2 Levels”, J. Biol. Chem. 278: 23343-23351
(2003).
157. Cheng, C., D.A. Lauffenburger, and T. Morales, “Motile
Chondrocytes: Migration Properties and Synthesis of Collagen II”,
Osteoarthr. Cart. 11: 603-612 (2003).
158. Mamoune, A., J.-H. Luo, D.A. Lauffenburger, and A. Wells, “Calpain-2
as a Target for Limiting Prostate Cancer Invasion”, Cancer
Res. 63: 4632-4640 (2003).
159. Janes, K.A., J.G. Albeck, L.X. Peng, P.K. Sorger, D.A. Lauffenburger,
and M.B. Yaffe, “High-Throughput Multiplex Kinase Assay for
Monitoring Information Flow in Signaling Networks: Application to
Sepsis-Apoptosis”, Molec. Cell. Proteomics 2: 463-473 (2003).
160. Hendriks, B., H.S. Wiley, and D.A. Lauffenburger, “HER2-Mediated
Effects on EGFR Endosomal Sorting: Analysis of Biophyical Mechanisms”,
Biophys. J. 85: 2732-2745 (2003).
161. Viswanathan, S., T. Benatar, M. Mileikovsky, D.A. Lauffenburger,
A. Nagy, and P.W. Zandstra, “Supplementation-Dependent Differences
in the Rates of Embryonic Stem Cell Self-Renewal, Differentiation,
and Apoptosis”, Biotech. Bioeng. 84: 505-517 (2003).
162. Rao, B.J., A.T. Girvin, T. Ciardelli, D.A. Lauffenburger, and
K.D. Wittrup, “Interleukin-2 Mutants with Enhanced a-Receptor
Subunit Binding Affinity”, Protein Eng. 16: 1081-10877 (2003).
163. Maly, I., H.S. Wiley, and D.A. Lauffenburger, “Self-Organization
of Polarized Cell Signaling via Autocrine EGFR Circuits: Computational
Model Analysis”, Biophys. J. 86: 10-22 (2004).
164. Prudhomme, W., K. Duggar, G.Q. Daly, P.W. Zandstra, and D.A.
Lauffenburger, “Multi-Variate Proteomic Analysis of Murine
Embryonic Stem Cell Self-Renewal vs Differentiation Behavior”,
Proc. Natl. Acad. Sci. USA 101: 2900-2905 (2004).
165. Iwabu, A., K. Smith, F.D. Allen, D.A. Lauffenburger, and A.
Wells, “EGF Induces Fibroblast Contractility and Motility
via a PKCd-Dependent Pathway”, J. Biol. Chem. (2004, accepted).
166. Janes, K.A., J. R. Kelly, S. Gaudet, J.G.Albeck, P.K. Sorger,
and D.A. Lauffenburger, “Cue-Signal-Response Analysis of TNF-Induced
Apoptosis by Partial Least Squares Regression of Dynamic Multi-Variate
Signaling Network Measurements”, J. Comp. Biol. (2004, accepted).
167. Prudhomme, W., K.H. Duggar, and D.A. Lauffenburger, “Kinetic
Model for Deconvolution of Murine Embryonic Stem Cell Self-Renewal
and Differentiation Responses to Cytokines and Extracellular Matrix”,
Biotech. Bioeng. (2004, accepted).
168. Tschumperlin, D.J., G. Dai, I.V. Maly, L.H. Laiho, A.K. McVittie,
P.T. So, D.A. Lauffenburger, R.D. Kamm, and J.M. Drazen, “Mechanotransduction
via Growth Factor Shedding into a Compliant Extracellular Space”,
Nature (2004, accepted).
169. Hendriks, B.S., A. Wells, H.S. Wiley, and D.A. Lauffenburger,
“Relative Contributions of Receptor Interactions and Endocytic
Trafficking Processes in Governing ERK Activation via the EGFR-HER2
System”, J. Biol. Chem. (2004, submitted).
170. Lu, H., L.Y. Koo, D.A. Lauffenburger, L.G. Griffith, and K.F.
Jensen, “Microfluidic Shear Devices for Quantitative Analysis
of Cell Adhesion”, Analyt. Chem. (2004, submitted).
171. Rao, B.M., I. Driver, D.A. Lauffenburger, and K.D. Wittrup,
“IL-2 Variants Engineered for Increased IL-2Ra Affinity Exhibit
Increased Potency Arising from a Cell Surface Ligand Reservoir Effect”,
Molec. Pharmacol. (2004, submitted).
172. Zaman, M., R.D. Kamm, P.T. Matsudaira, and D.A. Lauffenburger,
“Computational Model for Cell Migration in 3-Dimensional Matrices”,
Biophys. J. (2004, submitted).
173. Maly, I., R.T. Lee, and D.A. Lauffenburger, “A Model
for Mechanotransduction in Cardiac Muscle: Effects of Extracellular
Matrix Deformation on Autocrine Signaling”, Ann. Biomed. Eng.
(2004, submitted).
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