Multidrug resistance (MDR)-associated transporters contribute to the persistence of many types of cancers during chemotherapy. Three decades of research to inhibit MDR-associated transporters have, so far, produced only limited benefits for cancer treatment. This proposal aims to develop functional assays that will make it possible to characterize better, and hence target effectively, MDR-associated transporters from cancer cells. This research will proceed in three steps. First, it will develop chip-based assay platforms for functional biophysical characterization of multidrug resistance-associated transporters. These assays will be combined with electrophysiology and single molecule fluorescence detection. Second, it will investigate, under well-controlled conditions, the effect of parameters that affect the transport rate, such as the transmembrane potential, the lipid composition, the concentration of ATP and co-transported molecules (e.g. glutathione) to understand better the function of MDR-associated transporters and possible ways to modulate this function. And third, it will develop assays that can monitor the transport rate of individual reconstituted MDR-associated transport proteins in planar lipid bilayers by taking advantage of extremely small volumes (picoliters) in microfabricated recording chips and by combining electrophysiology with single molecule optical detection. We will use these assays to characterize MDR-associated transporters on the single-protein-level in analogy to single ion channel patch clamp recordings. Finally we aim to investigate the activation state and the effect of activation (e.g. by phosphorylation) on the single transporter efflux rates.
Yusko, Erik C; Bruhn, Brandon R; Eggenberger, Olivia M et al. (2017) Real-time shape approximation and fingerprinting of single proteins using a nanopore. Nat Nanotechnol 12:360-367 |
Horger, Kim S; Liu, Haiyan; Rao, Divya K et al. (2015) Hydrogel-assisted functional reconstitution of human P-glycoprotein (ABCB1) in giant liposomes. Biochim Biophys Acta 1848:643-53 |
Rao, Divya K; Liu, Haiyan; Ambudkar, Suresh V et al. (2014) A combination of curcumin with either gramicidin or ouabain selectively kills cells that express the multidrug resistance-linked ABCG2 transporter. J Biol Chem 289:31397-410 |
Majd, Sheereen; Yusko, Erik C; Yang, Jerry et al. (2013) A model for the interfacial kinetics of phospholipase D activity on long-chain lipids. Biophys J 105:146-53 |
Langecker, Martin; Arnaut, Vera; Martin, Thomas G et al. (2012) Synthetic lipid membrane channels formed by designed DNA nanostructures. Science 338:932-6 |
Fan, Zhenzhen; Liu, Haiyan; Mayer, Michael et al. (2012) Spatiotemporally controlled single cell sonoporation. Proc Natl Acad Sci U S A 109:16486-91 |
Yusko, Erik C; Prangkio, Panchika; Sept, David et al. (2012) Single-particle characterization of Aýý oligomers in solution. ACS Nano 6:5909-19 |
Yusko, Erik C; Johnson, Jay M; Majd, Sheereen et al. (2011) Controlling protein translocation through nanopores with bio-inspired fluid walls. Nat Nanotechnol 6:253-60 |
Majd, Sheereen; Yusko, Erik C; Billeh, Yazan N et al. (2010) Applications of biological pores in nanomedicine, sensing, and nanoelectronics. Curr Opin Biotechnol 21:439-76 |
Majd, Sheereen; Yusko, Erik C; MacBriar, Alexander D et al. (2009) Gramicidin pores report the activity of membrane-active enzymes. J Am Chem Soc 131:16119-26 |
Showing the most recent 10 out of 12 publications