出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/01/24 05:15:44」(JST)
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The voltage clamp is is an experimental method used by electrophysiologists to measure the ion currents through the membranes of excitable cells, such as neurons, while holding the membrane voltage at a set level. A basic voltage clamp will iteratively measure the membrane potential, and then change the membrane potential (voltage) to a desired value by adding the necessary current. This "clamps" the cell membrane at a desired constant voltage, allowing the voltage clamp to record what currents are delivered. Because the currents applied to the cell must be equal to (and opposite in charge to) the current going across the cell membrane at the set voltage, the recorded currents indicate how the cell reacts to changes in membrane potential.[1] Cell membranes of excitable cells contain many different kinds of ion channels, some of which are voltage-gated. The voltage clamp allows the membrane voltage to be manipulated independently of the ionic currents, allowing the current-voltage relationships of membrane channels to be studied.[2]
The concept of the voltage clamp is attributed to Kenneth Cole[3] and George Marmont[4] in the spring of 1947.[5] They inserted an internal electrode into the giant axon of a squid and began to apply a current. Cole discovered that it was possible to use two electrodes and a feedback circuit to keep the cell's membrane potential at a level set by the experimenter.
Cole developed the voltage clamp technique before the era of microelectrodes, so his two electrodes consisted of fine wires twisted around an insulating rod. Because this type of electrode could be inserted into only the largest cells, early electrophysiological experiments were conducted almost exclusively on squid axons.
Squids squirt jets of water when they need to move quickly, as when escaping a predator. To make this escape as fast as possible, they have an axon that can reach 1 mm in diameter (signals propagate more quickly down large axons). The squid giant axon was the first preparation that could be used to voltage clamp a transmembrane current, and it was the basis of Hodgkin and Huxley's pioneering experiments on the properties of the action potential.[5]
Alan Hodgkin realized that, to understand ion flux across the membrane, it was necessary to eliminate differences in membrane potential.[6] Using experiments with the voltage clamp, Hodgkin and Andrew Huxley published 5 papers in the summer of 1952 describing how ionic currents give rise to the action potential.[7] The final paper proposed the Hodgkin–Huxley model which mathematically describes the action potential. The use of voltage clamps in their experiments to study and model the action potential in detail has laid the foundation for electrophysiology; for which they shared the 1963 Nobel Prize in Physiology or Medicine.[6]
The voltage clamp is a current generator. Transmembrane voltage is recorded through a "voltage electrode", relative to ground, and a "current electrode" passes current into the cell. The experimenter sets a "holding voltage", or "command potential", and the voltage clamp uses negative feedback to maintain the cell at this voltage. The electrodes are connected to an amplifier, which measures membrane potential and feeds the signal into a feedback amplifier. This amplifier also gets an input from the signal generator that determines the command potential, and it subtracts the membrane potential from the command potential (Vcommand – Vm), magnifies any difference, and sends an output to the current electrode. Whenever the cell deviates from the holding voltage, the operational amplifier generates an "error signal", that is the difference between the command potential and the actual voltage of the cell. The feedback circuit passes current into the cell to reduce the error signal to zero. Thus, the clamp circuit produces a current equal and opposite to the ionic current.
The two-electrode voltage clamp (TEVC) technique is used to study properties of membrane proteins, especially ion channels.[8] Researchers use this method most commonly to investigate membrane structures expressed in Xenopus oocytes. The large size of these oocytes allows for easy handling and manipulability.[9] When a solution is applied to the cell, ion channels open up, which affects the flow of ions through the membrane. By taking a reading of the changes in ion current, scientists can determine how cells are affected by a neurotransmitter, antibiotic, etc. This provides clues about the mechanisms of certain proteins or channels.
The TEVC method utilizes two low-resistance pipettes, one sensing voltage and the other injecting current. The microelectrodes are filled with conductive solution and injected into the cell membrane to artificially control membrane potential. The membrane acts as a dielectric as well as a resistor, while the fluids on either side of the membrane function as capacitors.[9] The microelectrodes compare the membrane potential against a command voltage, giving an accurate reproduction of the currents flowing across the membrane. Current readings can then be used to analyze the electrical response of the cell to different applications.
This technique is favored over single-microelectrode clamp or other voltage clamp techniques when conditions call for resolving large currents. The high current-passing capacity of the two-electrode clamp makes it possible to clamp large currents that are impossible to control with single-electrode patch techniques.[10] The two-electrode system is also desirable for its fast clamp settling time and low noise. However, TEVC is limited in use with regard to cell size. It is effective in larger-diameter oocytes, but more difficult to use with small cells. Additionally, TEVC method is limited in that the transmitter of current must be contained in the pipette. It is not possible to manipulate the intracellular fluid while clamping, which is possible using patch clamp techniques.[11] Another disadvantage involves "space clamp" issues. Cole's voltage clamp used a long wire that clamped the squid axon uniformly along its entire length. TEVC microelectrodes can provide only a spatial point source of current that may not uniformly affect all parts of an irregularly shaped cell.
The dual-cell voltage clamp technique is a specialized variation of the two electrode voltage clamp, and is only used in the study of gap junction channels.[12] Gap junctions are pores that directly link two cells through which ions and small metabolites flow freely. When two cells in which gap junction proteins are expressed either endogenously or via injection of mRNA, a junction channel will form between the cells. Since two cells are present in the system, two sets of electrodes are used. A recording electrode and a current injecting electrode are inserted into each cell, and each cell is clamped individually (each set of electrodes is attached to a separate apparatus, and integration of data is performed by computer). To record junctional conductance, the current is varied in the first cell while the recording electrode in the second cell records any changes in Vm for the second cell only. (The process can be reversed with the stimulus occurring in the second cell and recording occurring in the first cell.) Since no variation in current is being induced by the electrode in the recorded cell, any change in voltage must be induced by current crossing into the recorded cell, through the gap junction channels, from the cell in which the current was varied.[12]
This category describes a set of techniques in which one electrode is inserted into the cell. This single electrode carries out the functions of both current injection and recording.
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The "patch-clamp" technique allows the study of individual ion channels. It uses an electrode with a relatively large tip (> 1 micrometer) that has a smooth surface (rather than a sharp tip). This is a "patch-clamp electrode" (as distinct from a "sharp electrode" used to impale cells). This electrode is pressed against a cell membrane and suction is applied to pull the cell's membrane inside the electrode tip. The suction causes the cell to form a tight seal with the electrode (a "gigaohm seal", as the resistance is more than a gigaohm).
SEV-c has the advantage is that you can record from small cells that would be impossible to impale with two electrodes. However:
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A single-electrode voltage clamp — discontinuous, or SEVC-d, has some advantages over SEVC-c for whole-cell recording. In this, a different approach is taken for passing current and recording voltage. A SEVC-d amplifier operates on a "time-sharing" basis, so the electrode regularly and frequently switches between passing current and measuring voltage. In effect, there are two electrodes, but each is in operation for only half of the time it is on. The oscillation between the two functions of the single electrode is termed a duty cycle. During each cycle, the amplifier measures the membrane potential and compares it with the holding potential. An operational amplifier measures the difference, and generates an error signal. This current is a mirror image of the current generated by the cell. The amplifier outputs feature sample and hold circuits, so each briefly sampled voltage is then held on the output until the next measurement in the next cycle. To be specific, the amplifier measures voltage in the first few microseconds of the cycle, generates the error signal, and spends the rest of the cycle passing current to reduce that error. At the start of the next cycle, voltage is measured again, a new error signal generated, current passed etc. The experimenter sets the cycle length, and it is possible to sample with periods as low as about 15 microseconds, corresponding to a 67 kHz switching frequency. Switching frequencies lower than about 10 kHz are not sufficient when working with action potentials that are less than 1 millisecond wide. Note that not all discontinuous voltage-clamp amplifier support switching frequencies higher than 10 kHz.[13]
For this to work, the cell capacitance must be higher than the electrode capacitance by at least an order of magnitude. Capacitance slows the kinetics (the rise and fall times) of currents. If the electrode capacitance is much less than that of the cell, then when current is passed through the electrode, the electrode voltage will change faster than the cell voltage. Thus, when current is injected and then turned off (at the end of a duty cycle), the electrode voltage will decay faster than the cell voltage. As soon as the electrode voltage asymptotes to the cell voltage, the voltage can be sampled (again) and the next amount of charge applied. Thus, the frequency of the duty cycle is limited to the speed at which the electrode voltage rises and decays while passing current. The lower the electrode capacitance the faster one can cycle.
SEVC-d has a major advantage over SEVC-c in allowing the experimenter to measure membrane potential, and, as it obviates passing current and measuring voltage at the same time, there is never a series resistance error. The main disadvantages are that the time resolution is limited and the amplifier is unstable. If it passes too much current, so that the goal voltage is over-shot, it reverses the polarity of the current in the next duty cycle. This causes it to undershoot the target voltage, so the next cycle reverses the polarity of the injected current again. This error can grow with each cycle until the amplifier oscillates out of control (“ringing”); this usually results in the destruction of the cell being recorded. The investigator wants a short duty cycle to improve temporal resolution; the amplifier has adjustable compensators that will make the electrode voltage decay faster, but, if these are set too high the amplifier will ring, so the investigator is always trying to “tune” the amplifier as close to the edge of uncontrolled oscillation as possible, in which case small changes in recording conditions can cause ringing. There are two solutions: to “back off” the amplifier settings into a safe range, or to be alert for signs that the amplifier is about to ring.
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