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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Functional site-directed fluorometry is a method to study protein domain motions in real time. Modification of this technique for its application in native cells now allows the detection and tracking of single voltage-sensor motions from voltage-gated Ca2+ channels in murine isolated skeletal muscle fibers.

Abstract

Functional site-directed fluorometry has been the technique of choice to investigate the structure-function relationship of numerous membrane proteins, including voltage-gated ion channels. This approach has been used primarily in heterologous expression systems to simultaneously measure membrane currents, the electrical manifestation of the channels' activity, and fluorescence measurements, reporting local domain rearrangements. Functional site-directed fluorometry combines electrophysiology, molecular biology, chemistry, and fluorescence into a single wide-ranging technique that permits the study of real-time structural rearrangements and function through fluorescence and electrophysiology, respectively. Typically, this approach requires an engineered voltage-gated membrane channel that contains a cysteine that can be tested by a thiol-reactive fluorescent dye. Until recently, the thiol-reactive chemistry used for the site-directed fluorescent labeling of proteins was carried out exclusively in Xenopus oocytes and cell lines, restricting the scope of the approach to primary non-excitable cells. This report describes the applicability of functional site-directed fluorometry in adult skeletal muscle cells to study the early steps of excitation-contraction coupling, the process by which muscle fiber electrical depolarization is linked to the activation of muscle contraction. The present protocol describes the methodologies to design and transfect cysteine-engineered voltage-gated Ca2+ channels (CaV1.1) into muscle fibers of the flexor digitorum brevis of adult mice using in vivo electroporation and the subsequent steps required for functional site-directed fluorometry measurements. This approach can be adapted to study other ion channels and proteins. The use of functional site-directed fluorometry of mammalian muscle is particularly relevant to studying basic mechanisms of excitability.

Introduction

The ability to track ion channel conformational rearrangements in response to a known electrical stimulus in a living cell is a source of valuable information for molecular physiology1. Voltage-gated ion channels are membrane proteins that sense changes in transmembrane voltage, and their function is also affected by voltage changes2. The development of voltage clamp techniques in the last century allowed physiologists to study, in real-time, ionic currents carried by voltage-gated ion channels in response to membrane depolarization3. The use of voltage clamp technology has been crucial in underst....

Protocol

This protocol was approved by the University of Maryland Institutional Animal Care and Use Committee. The following protocol has been divided into multiple subsections, consisting of (1) molecular construct design and cysteine reacting dye selection, (2) in vivo electroporation, (3) muscle dissection and fiber isolation, (4) acquisition setup description, (5) assessment of enhanced green fluorescent protein (EGFP) positive fiber electrical activity and cysteine staining, and (6) signal acquisition and processing.......

Representative Results

When propagating action potentials are triggered in response to repetitive field stimulation, it is possible to track specific voltage sensor motion in response to a specific frequency of depolarization. As shown in Figure 6A, the motion of VSD-II-tagged helices can be tracked in response to each of two successive depolarizations applied at 10 Hz (i.e., spaced by 100 ms). Signal bleaching can be corrected by subtracting baseline to the trace (Figure 6B). Further.......

Discussion

Here, a step-by-step protocol to conduct FSDF in muscle fibers for the study of individual voltage sensor motions from the CaV1.1 channel is described. Even though the number of steps and the diversity of approaches that are combined in this technique may appear complex, most of these techniques are often routinely used in biophysicist/cell biologist laboratories. Thus, the apparent complexity resides mainly in the combination of all the various approaches in a single integrated technique. Often when carrying .......

Acknowledgements

We thank Dr. J. Vergara (University of California, Los Angeles) for sharing the EGFP-CaV1.1 (rabbit) wild-type plasmid. We thank the Yale Department of Physiology Electronics Laboratory and especially Henrik Abildgaard for the design and construction of the photodiode with track and hold circuit. This work was supported by the National Institutes of Health grants R01-AR075726 and R01-NS103777

....

Materials

NameCompanyCatalog NumberComments
HyaluronidaseSIGMA ALDRICHH3884-50mg
0.5 mL Eppendorf tubeMillipore SigmaEP022363719-500EA
1 mL syringeMillipore SigmaZ683531-100EAtuberculine slip tip
1/2” long 29-gauge sterile insulin needle and syringeBecton Dikinson324702
35 mm non coated plastic plateFalcon, Corning353001
60 mm non coated plastic plateFalcon, Corning351007
Alcoholic whipPDIB60307
Alexa-533 cube LPChroma49907Ex: 530/30x; BS: 532; Em: 550lp
Arc lampSutter InstrumetsLB-LS 672
Artificial tears creamAkornNDC 59399-162-35
Borosilicate glass Pasteur pipet 5 3/4"VWR14672-200
BTS (N-benzyl-p-toluene sulphonamide)SIGMA ALDRICH203895
collagenase type ISIGMA ALDRICHC0130-1g
Cotton tipVWRVWR-76048-960-BG
Double electrode array  (for electroporation)BTX harvard apparatus45-012010mm 2 needle array tips
EGFP cubeChroma39002ATEx: 480/30x; BS 505; Em: 535/40m
Electroporation apparatus deviceBTX harvard apparatusECM 830
EPC10HEKA Elektronik GmbH  (Harvard Bioscience)895000
FBSBiotechne,  R&D SystemsRND-S11150HFetal Bovine Serum - Premium, Heat Inactivated
glass coverslip 35 mm dishMatTek Life ScienceP35G-1.5-14-C
IsofluraneFluriso (Isoflurane) Liquid for Inhalation502017-250ml
Isothermal heating padBraintree scientific inc39DP
LamininThermo FisherINV-23017015Laminin Mouse Protein, Natural
Latex bulbVWR82024-554
LED 530 nmSutter Instrumets5A-530
Low binding protein 0.2 μm sterile filterPallFG4579acrodisk  syringe filter 0.2um supor membrane low protein binding non pyrogenic
MEMInvitrogenINV-11380037
MTS-5-TAMRABiotium89410-784MTS-5-TAMRA
OriginPro Analysis SoftwareOriginLab CorporationOriginPro 2022 (64-bit) SR1
PhotodiodeCustom MadeNA
PlanApo 60x oil  1.4 N.A/∞/0.17OlympusBFPC2
Platinum wire 0.5 mm, 99.9 % metals basisSIGMA267228-1GTo manufacyte field stimulation electrode
Pulse GeneratorWPIPulsemaster A300
Shutter drive controllerUniblitz100-2B
ShuttterUniblitzVS2582T0-100
S-MEMInvitrogenINV-11380037
Sterile bench padVWRDSI-B1623
Sterile salineSIGMA ALDRICHS8776
Sylgard 184 Silicone Elastomer kitDow Corning1419447-1198
Vaporizer for AnesthesiaParkland ScientificV3000PK
Voltage generatorCustom MadeNA

References

  1. Catterall, W. A., Wisedchaisri, G., Zheng, N. The chemical basis for electrical signaling. Nature Chemical Biology. 13 (5), 455-463 (2017).
  2. Armstrong, C. M., Hille, B. Voltage-gated ion channels and electrical excitability.

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