The chemistrode: A droplet-based microfluidic device for stimulation and recording with high temporal, spatial, and chemical resolution
Abstract
Microelectrodes enable localized electrical stimulation and recording, and they have revolutionized our understanding of the spatiotemporal dynamics of systems that generate or respond to electrical signals. However, such comprehensive understanding of systems that rely on molecular signals—e.g., chemical communication in multicellular neural, developmental, or immune systems—remains elusive because of the inability to deliver, capture, and interpret complex chemical information. To overcome this challenge, we developed the ''chemistrode,'' a plug-based microfluidic device that enables stimulation, recording, and analysis of molecular signals with high spatial and temporal resolution. Stimulation with and recording of pulses as short as 50 ms was demonstrated. A pair of chemistrodes fabricated by multilayer soft lithography recorded independent signals from 2 locations separated by 15 μm. Like an electrode, the chemistrode does not need to be built into an experimental system—it is simply brought into contact with a chemical or biological substrate, and, instead of electrical signals, molecular signals are exchanged. Recorded molecular signals can be injected with additional reagents and analyzed off-line by multiple, independent techniques in parallel (e.g., fluorescence correlation spectroscopy, MALDI-MS, and fluorescence microscopy). When recombined, these analyses provide a time-resolved chemical record of a system's response to stimulation. Insulin secretion from a single murine islet of Langerhans was measured at a frequency of 0.67 Hz by using the chemistrode. This article characterizes and tests the physical principles that govern the operation of the chemistrode to enable its application to probing local dynamics of chemically responsive matter in chemistry and biology.
Additional Information
© 2008 by The National Academy of Sciences of the USA. Published online before print October 30, 2008. We thank Vytas Bindokas for help with confocal microscopy and Jessica M. Price for contributions in writing and editing this manuscript. This work was supported by National Institutes of Health (NIH) Director's Pioneer Award 1DP1OD003584 and National Science Foundation (NSF) Collaborative Research in Chemistry Grant CHE-0526693 (to R.F.I.), NIH Grants DK48494, DK63493, and DK20595 (to L.H.P.) and the Blum–Kovler Foundation (L.H.P.). R.F.I. is a Cottrell Scholar of Research Corporation and a Camille Dreyfus Teacher–Scholar. A part of this work was performed at the Materials Research Science and Engineering Center microfluidic facility funded by the NSF. Author contributions: D.C., W.D., Y.L., W.L., A.K., L.H.P., and R.F.I. designed research; D.C., W.D., Y.L., W.L., and F.E.M. performed research; D.C., W.D., Y.L., W.L., A.K., L.H.P., and R.F.I. analyzed data; and D.C., W.D., Y.L., W.L., and R.F.I. wrote the paper. The authors declare no conflict of interest. This article is a PNAS Direct Submission. This article contains supporting information online at www.pnas.org/cgi/content/full/0807916105/DCSupplemental.Attached Files
Published - Ismagilov_PNAS_2008_105_16843_Chemistrode.pdf
Supplemental Material - Ismagilov_PNAS_2008_105_16843_Chemistrode_SI.pdf
Supplemental Material - SM1.mov
Supplemental Material - SM2.mov
Supplemental Material - SM3.mov
Supplemental Material - SM4.mov
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Additional details
- PMCID
- PMC2579341
- Eprint ID
- 40783
- Resolver ID
- CaltechAUTHORS:20130821-160717046
- NIH
- 1DP1 OD003584
- NSF
- CHE-0526693
- NIH
- DK48494
- NIH
- DK63493
- NIH
- DK20595
- Blum–Kovler Foundation
- Cottrell Scholar of Research Corporation
- Camille and Henry Dreyfus Foundation
- Created
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2013-08-27Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field