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Rapid Temperature Jump by Infrared Diode Laser Irradiation for Patch-Clamp Studies

Identifieur interne : 000265 ( Pmc/Corpus ); précédent : 000264; suivant : 000266

Rapid Temperature Jump by Infrared Diode Laser Irradiation for Patch-Clamp Studies

Auteurs : Jing Yao ; Beiying Liu ; Feng Qin

Source :

RBID : PMC:2711624

Abstract

Several thermal TRP ion channels have recently been identified. These channels are directly gated by temperature, but the mechanisms have remained elusive. Studies of their temperature gating have been impeded by lack of methods for rapid alteration of temperature in live cells. As a result, only measurements of steady-state properties have been possible. To solve the problem, we have developed an optical approach that uses recently available infrared diode lasers as heat sources. By restricting laser irradiation around a single cell, our approach can produce constant temperature jumps over 50°C in submilliseconds. Experiments with several heat-gated ion channels (TRPV1–3) show its applicability for rapid temperature perturbation in both single cells and membrane patches. Compared with other laser heating approaches such as those by Raman-shifting of the Nd:YAG fundamentals, our approach has the advantage of being cost effective and applicable to live cells while providing an adequate resolution for time-resolved detection of channel activation.


Url:
DOI: 10.1016/j.bpj.2009.02.016
PubMed: 19413966
PubMed Central: 2711624

Links to Exploration step

PMC:2711624

Le document en format XML

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<p>Several thermal TRP ion channels have recently been identified. These channels are directly gated by temperature, but the mechanisms have remained elusive. Studies of their temperature gating have been impeded by lack of methods for rapid alteration of temperature in live cells. As a result, only measurements of steady-state properties have been possible. To solve the problem, we have developed an optical approach that uses recently available infrared diode lasers as heat sources. By restricting laser irradiation around a single cell, our approach can produce constant temperature jumps over 50°C in submilliseconds. Experiments with several heat-gated ion channels (TRPV1–3) show its applicability for rapid temperature perturbation in both single cells and membrane patches. Compared with other laser heating approaches such as those by Raman-shifting of the Nd:YAG fundamentals, our approach has the advantage of being cost effective and applicable to live cells while providing an adequate resolution for time-resolved detection of channel activation.</p>
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<article-title>Rapid Temperature Jump by Infrared Diode Laser Irradiation for Patch-Clamp Studies</article-title>
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<email>qin@buffalo.edu</email>
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<aff>Department of Physiology and Biophysical Sciences, State University of New York at Buffalo, Buffalo, New York 14214</aff>
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Corresponding author
<email>qin@buffalo.edu</email>
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<issue>9</issue>
<fpage>3611</fpage>
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<date date-type="received">
<day>16</day>
<month>1</month>
<year>2009</year>
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<day>11</day>
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<copyright-statement>© 2009 by the Biophysical Society.</copyright-statement>
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<abstract>
<p>Several thermal TRP ion channels have recently been identified. These channels are directly gated by temperature, but the mechanisms have remained elusive. Studies of their temperature gating have been impeded by lack of methods for rapid alteration of temperature in live cells. As a result, only measurements of steady-state properties have been possible. To solve the problem, we have developed an optical approach that uses recently available infrared diode lasers as heat sources. By restricting laser irradiation around a single cell, our approach can produce constant temperature jumps over 50°C in submilliseconds. Experiments with several heat-gated ion channels (TRPV1–3) show its applicability for rapid temperature perturbation in both single cells and membrane patches. Compared with other laser heating approaches such as those by Raman-shifting of the Nd:YAG fundamentals, our approach has the advantage of being cost effective and applicable to live cells while providing an adequate resolution for time-resolved detection of channel activation.</p>
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