Biomimetic Chemical Sensors Using Nanoelectronic Readout of Olfactory Receptor Proteins

被引:126
作者
Goldsmith, Brett R. [1 ]
Mitala, Joseph J., Jr. [2 ,3 ]
Josue, Jesusa [4 ]
Castro, Ana [5 ]
Lerner, Mitchell B. [1 ]
Bayburt, Timothy H. [6 ]
Khamis, Samuel M. [7 ]
Jones, Ryan A. [7 ]
Brand, Joseph G. [4 ]
Sligar, Stephen G. [6 ]
Luetje, Charles W. [5 ]
Gelperin, Alan [4 ,8 ]
Rhodes, Paul A. [7 ,9 ]
Discher, Bohdana M. [2 ,3 ]
Johnson, A. T. Charlie [1 ,2 ]
机构
[1] Univ Penn, Dept Phys & Astron, Philadelphia, PA 19104 USA
[2] Univ Penn, Nano Bio Interface Ctr, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
[4] Monell Chem Senses Ctr, Philadelphia, PA 19104 USA
[5] Univ Miami, Dept Mol & Cellular Pharmacol, Miami, FL 33101 USA
[6] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
[7] Nanosense Inc, Redwood City, CA 94063 USA
[8] Princeton Univ, Princeton Neurosci Inst, Dept Mol Biol, Princeton, NJ 08544 USA
[9] Evolved Machines LLC, Palo Alto, CA 94301 USA
关键词
bioelectronics; vapor sensor; olfactory receptor proteins; field effect transistor; nanotube; PHOSPHOLIPID-BILAYER NANODISCS; WALLED CARBON NANOTUBES; MEMBRANE-PROTEINS; FUNCTIONALIZATION; MOUSE; RECONSTITUTION; PHEROMONES; EXPRESSION; MECHANISM; DEVICES;
D O I
10.1021/nn200489j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have designed and implemented a practical nanoelectronic interface to G-protein coupled receptors (GPCRs), a large family of membrane proteins whose roles in the detection of molecules outside eukaryotic cells make them important pharmaceutical targets. Specifically, we have coupled olfactory receptor proteins (ORs) with carbon nanotube transistors. The resulting devices transduce signals associated with odorant binding to ORs in the gas phase under ambient conditions and show responses that are in excellent agreement with results from established assays for OR ligand binding. The work represents significant progress on a path toward a bioelectronic nose that can be directly compared to biological olfactory systems as well as a general method for the study of GPCR function in multiple domains using electronic readout.
引用
收藏
页码:5408 / 5416
页数:9
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