Mini Matrix System
5-Channel Single Electrode System
The multielectrode manipulator "Mini Matrix" was developed by Thomas RECORDING in 1998. This microdrive system is based on our patented rubber tube drive also used in our multielectrode manipulator "System Eckhorn".
The small and lightweight multielectrode manipulator "Mini Matrix" was designed to be mounted directly on a monkey head but also can be used with stereotaxic instruments available from Thomas RECORDING.
The 5-Channel Single Electrode System can use up to 5 single electrodes at the same time.
- Axial resolution better than 1μm, x-y-z-Positioning with xyz-manipulator and special holder
- Patented rubber-tube drive, no hysteresis, slick or free motion due to patented rubber tube drive (avoids drawbacks of cable, direct or hydraulic driven systems)
- Electrode travel range up to 24.000μm
- Variable speed range from 0...250μm/s, higher velocity on request
- Small and lightweight
- No electrode connection cables free in air! Complete metal shield around all microelectrodes
- Suitable for cortical and deep brain recordings
- Very close electrode spacing available (down to 80μm)
- Different electrode arrangements available (linear, concentric, etc.)
- Stable long-term recordings with thin microelectrodes for hours
- Integrated low noise preamplifier
With this fiber-electrode manipulator type Mini Matrix a broad range of even very thin shafted probes can be handled, including fiber and wire-electrodes with shaft diameters down to about 25 µm. The patented driving principle of the Mini Matrix offers an outstanding electrode positioning accuracy. Compared with hydraulic, cable controlled or direct motor driven microdrives, the patented fiber electrode manipulator "System Eckhorn" does not cause hysteresis errors of the electrode movement. Hysteresis error is generally a result of stiction and free motion of hydraulic, cable controlled or direct motor driven microdrives offered by our competitors. Our system has a higher degree of positioning accuracy due to its patented rubber tube driving mechanism being almost absolutely free of stiction and free motion.
Using Thomas Mini Matrix systems with patented rubber tube drive allows to record neural activity while the electrode is moving in the brain. So it is very easy to search active neurons in the brain.
The Thomas Mini Matrix systems have some advantages in comparison to other multielectrode microdrive systems for neurophysiological research presently available on the market:
- Vibration-free positioning of up to 5 quartz-platinum/tungsten microelectrodes in 1µm steps
- Patented rubber tube driving principle
- High positioning accuracy, due to lack of stiction and free motion
- Easy exchange and calibration of microelectrodes within minutes
- Advances up to 5 microelectrodes/tetrodes independently in 1µm steps up to 24.000µm (other electrode travel distances on request!)
- Xyz-manipulator travel-distance: z=0-30mm, x= ±10mm, y=±10mm
- Continuous low noise recording while the electrode scans the tissue at low velocity,
- No noise introduction in the recordings so that you can search active neurons in the brain
- No electrode connection cables free in air, no electrical noise pickup from environment (e.g. motors, radio stations)! Competitor drives pickup electrical interference from the environment so that you for example can hear radio station music or electrical artifacts from lab devices from the audio monitor loudspeaker instead of neural spikes!
- Electrode moving velocity adjustable (1-250µm/s), moving direction selectable
- Microdrive with xyz-manipulator is small and lightweight
- Low noise 5 channel preamplifier is integrated into the microdrive chassis, system is completely shielded to avoid electrical noise pickup from the environment, three preamplifier operation modes: record, electrode impedance test, electrical stimulation/lesioning
- System is completely delivered with motor control device, integrated preamplifier, software, xyz-manipulator, chamber holder, exchangeable head, handheld remote control, etc.
- Exchangeable manipulator head allows manifold electrode configurations and interelectrode spacings
- Electrode spacings from 80µm up to some millimeters possible due to exchangeable Mini Matrix heads
- The system is modular and adaptable to the end user´s requirements.
- The Mini Matrix is usable for cortical as well as deep brain recordings in all kinds of research applications
- User friendly computer controlled system with LAN (local area network) communication via TCP/IP protocol between motor control unit and personal computer. Software package is part of the system.
- Using very thin shaft Thomas microelectrodes (outer diameter 80µm) causes minimal tissue damage.
- Different neurophysiological methods are available for the Mini Matrix systems (e.g. optogenetics, microinjection)
The Mini Matrix system is available for small animal stereotaxic instruments (see figure 3 and 4) as well as for primate experiments (see figure 2).
Each Mini Matrix microdrive is equipped with an exchangeable Microdrive head. Each Mini Matrix head has up to 5 electrode guide tubes. There are different possibilities to arrange these 5 guide tubes, depending on the recording area. Basically we have exchangeable heads for cortical, deep brain or spinal cord recordings.
It is very easy to exchange a Mini Matrix head by another one with other electrode guide tube arrangement or electrode guide tube spacing. The following picture demonstrates the exchange procedure.
Heads for cortical recordings
There are four parameters of an exchangeable Mini Matrix head that can be customized:
- protrusion of the electrode guide tubes
- arrangement of the guide tube (e.g. linear, concentric, etc.)
- guide tube spacing (e.g. 305µm, 500µm. etc.)
- Sharpened of non-sharpened (standard) guide tubes for dura penetration
The standard guide tube protrusion for an exchangeable head for cortical recordings is x=8mm, which is optimal for most recording applications (e.g. rats, mice, rodents, etc.). If you are using deep primate recording chambers we can adapt the guide tube protrusion to the depth of the primate recording chamber.
Heads for deep brain recordings
For deep brain recording applications in small animals the normal electrode travel distance of a Mini Matrix system of 22-24 mm is enough to reach the deep brain target in rats, without introducing a cannula in the brain. For larger animals such as primates the use of a common guiding cannula with minimized outer diameter is required to bring up to 5 microelectrodes down to the recording target. Therefore we offer a special cannula technique for our Mini Matrix, invented by Dr. David Leopold (NIMH, USA). We call this technique the “Leopold Funnel Adapter”.
Please feel free to ask for your customized deep brain recording solution!
Heads for spinal cord recordings
Microdrive heads for spinal cord recording have a linear guide tube arrangement and interelectrode spacings from 305µm up to 10mm, depending on the researcher´s requirements.
Electrical Stimulation and Impedance Test
The MSD is equipped with a special low current impedance test unit that allows measuring the electrode tissue impedance of each microelectrode while the electrode is in the brain. The constant current is so low (5nA) that it does not stimulate nerve cells in the brain. The electrode impedance value is displayed on a moving coil instrument. We have used this kind of instrument instead of digital because moving coil instruments better display fluctuations in the impedance value which is important especially when electrodes penetrate tissue borders (e.g. primate dura mater).
The preamplifiers of our Mini Matrix systems are prepared for electrical stimulation and lesioning. You can pass a stimulus or lesioning current through each of the 5 microelectrodes. A Mode Selection & Impedance Test Device (MSD, see figure 12) is required as well as a microstimulation generator. Both devices are available from TREC on request.
Especially for microstimulation we offer special coated Thomas microelectrodes. The microstimulation electrode tips are coated with iridium oxide. This coating increases the charge transfer capacity of our electrodes dramatically which makes them very well suited for stimulation experiments.
Setting lesions with Thomas microelectrodes
At the end of a recording session you might want to mark the recording position of the recording electrode. In this case you can pass a lesion current through our standard microelectrode tip. It could be shown by Robert Shapley and colleagues, that small dc currents make good lesions in primate visual cortex without any electrode tip damage (see unpublished report).
Microinjection with the Mini Matrix
For making drug injection experiments with the Thomas Mini Matrix system we offer a special designed high pressure microinjection system. One of the 5 single microelectrodes of the Mini Matrix can be replaced by a microinjection cannula. The microinjection cannula (OD=120µm) has a tapered tip and is equipped with the patented Thomas rubber tube drive so that you can position the microinjection cannula tip together with the recording microelectrodes with high positioning accuracy (better than 1µm). The microinjection system consists of a special designed and computer controlled syringe pump that is connected to the microinjection cannula via a special thick wall tubing.
The precision micromotor of the microinjection pump is controlled by the same motor control unit and graphical user interface as the Thomas Mini Matrix. This guarantees a high precision and convenient experimental control of the injection/recording experiment.
Optogenetic equipment for the Mini Matrix
Thomas RECORDING offers a complete range of Mini Matrix accessories for optogenetic experiments. One of the 5 single microelectrodes or tetrodes is replaced by an optical fiber (OD=120µm). The optical fiber has a tapered tip and is equipped with the patented Thomas rubber tube drive so that you can position the optical fiber tip together with the recording microelectrodes with high positioning accuracy (better than 1µm). Figure 14 shows a Mini Matrix head with concentric guide tube arrangement and a single optical fiber in the center position. The recording microelectrodes are concentrically arrange around the optical fiber in the center of this arrangement.
In figure 15 one can see a Thomas Mini Matrix equipped with a LED-light source holder. In figure 16 an optical fiber is loaded to the Mini Matrix.
For further information concerning optogenetic equipment please see also our optogenetic webpage.
 Bessaih T., Higley M. J., Contreras D. Millisecond precision temporal encoding of stimulus features during cortically generated gamma oscillations in the rat somatosensory cortex. The Journal of Physiology 596(3): 515-534, February 2018, DOI: 10.1113/JP275245
 Yao T., Treue S., Krishna S. Saccade-synchronized rapid attention shifts in macaque visual cortical area MT. Nature Communications 9, Article number: 958 (2018), DOI: 10.1038/s41467-018-03398-3
 Martínez-Vázquez P., Gail A. Directed Interaction Between Monkey Premotor and Posterior Parietal Cortex During Motor-Goal Retrieval from Working Memory. Cerebral Cortex, 2018, 1-16, DOI: 10.1093/cercor/bhy035
 Piserchia V., Breveglieri R., Hadjidimitrakis K., Bertozzi F., Galletti C., Fattori P. Mixed Body/Hand Reference Frame for Reaching in 3D Space in Macaque Parietal Area PEc. Cerebral Cortex, Volume 27 Issue 3 Pages 1976-1990, March 2017, DOI: 10.1093/cercor/bhw039
 Hadjidimitrakis K., Bertozzi F., Breveglieri R., Galletti C., Fattori P. Temporal stability of reference frames in monkey area V6A during a reaching task in 3D space. Brain Struct Funct., 222(4): 1959-1970; May 2017, DOI: 10.1007/s00429-016-1319-5
 Falcone R., Cirillo R., Ferraina S., Genovesio A. Neural activity in macaque medial frontal cortex represents others’ choices. Scientific Reports 7, Article number: 12663, October 2017, DOI: 10.1038/s41598-017-12822-5
 Dominguez-Vargas A., Schneider L., Wilke M., Kagan I. Electrical Microstimulation of the Pulvinar Biases Saccade Choices and Reaction Times in a Time-Dependent Manner. Journal of Neuroscience, 37 (8), February 2017, DOI: 10.1523/JNEUROSCI.1984-16.2016
 Ma X., Ma C., Huang J., Zhang P., Xu J., He J. Decoding Lower Limb Muscle Activity and Kinematics from Cortical Neural Spike Trains during Monkey Performing Stand and Squat Movements. Front. Neurosci., February 2017, DOI: 10.3389/fnins.2017.00044
 Knyezva S., Selezneva E., Gorkin A., Aggelopoulos N. C., Brosch M. Neuronal Correlates of Auditory Streaming in Monkey Aduitory Cortex for Tone Sequences without Spectral Differences. Front. Integr. Neurosci. January 2018, DOI: 10.3389/fnint.2018.00004
 Michaels J. A., Scherberger H. Population coding of grasp and laterality-related information in the macaque fronto-parietal network. Scientific Reports 8 Article number: 1710, January 2018, DOI: 10.1038/s41598-018-20051-7
 Klein C., Evrard H. C., Shapcott K. A., Haverkamp S., Logothetis N. K., Schmid M. C. Cell-Targeted Optogenetics and Electrical Microstimulation Reveal the Primate Koniocellular Projection to Supra-granular Visual Cortex. Neuron Volume 90 Issue 1 Pages 143-151, April 2016, DOI: 10.1016/j.neuron.2016.02.036
 Esghaei M., Daliri M.R., Treue S. Local field potentials are induced by visually evoked spiking activity in macaque cortical area MT Scientific Reports 7, Article number 17110, December 2017, DOI: 10.1038/s41598-017-17372-4
 Huidobro N., De la Torre-Valdovinos B., Mendez A., Treviño M., Arias-Carrion O., Chavez F., Gutierrez R., Manjarrez E. Optogenetic noise-photostimulation on the brain increases somatosensory spike firing responses Neuroscience Letters (2018), Volume 664, pages 51-57, DOI: 10.1016/j.neulet.2017.11.004
 Middelton J. W., Simons D. J., Simmons J. W., Clarb R. S. B., Kochanek P. M., Shoykhet M. Long-Term Deficits in Cortical Circuit Function after Asphyxial Cardiac Arrest and Resuscitation in Developing Rats eNeuro (2017), 4(3) e0319-16.2017 1-18, DOI: 10.1523/ENEURO.0319-16.2017
 Bizley J. K., Walker K. M. M., King A. J., Schnupp J. W. H. Neural Ensemble Codes for Stimulus Periodicity in Auditory Cortex The Journal of Neuroscience, April 2010, 30(14):5078 –5091
 Anderson B., Harrison M., Sheinberg D. L. A multielectrode study of the inferotemporal cortex in the monkey: effects of grouping on spike rates and synchrony Neuroreport, March 2006, Vol 17 No 4
 Maier A., Wilke M., Aura C., Zhu C., Ye F. Q., Leopold D. A. Divergence of fMRI and neural signals in V1 during perceptual suppression in the awake monkey Nat Neurosci, October 2008, 11(10): 1193–1200
 Wang O., Webber R. M., Stanley G. B.Thalamic Synchrony and the Adaptive Gating of Information Flow to Cortex Nat Neurosci, December 2010 , 13(12): 1534–1541
 Adams D. L., Horton J. C. Monocular Cells Without Ocular Dominance Columns J Neurophysiol, 2006 , 96: 2253–2264
 Schoppik D., Nagel K.I., Lisberger S.G. Cortical Mechanisms of Smooth Eye Movements Revealed by Dynamic Covariations of Neural and Behavioral Responses Neuron, April 2008 , 58(2): 248–260
 Hohl S. S., Lisberger S.G. Representation of Perceptually Invisible Image Motion in Extrastriate Visual Area MT of Macaque Monkeys The Journal of Neuroscience, November 2011 , 31(46):16561–16569
 Law C., Gold J. I. Neural correlates of perceptual learning in a sensorymotor, but not a sensory, cortical area Nat Neurosci, 2008 April , 11(4): 505–513.
 Castellanos L. Grasping in Primates: Mechanics and Neural Basis
 Lee C. W., King C. E. , Wu S. C., A. Swindlehurst L., Nenadic Z. Signal Source Localization with Tetrodes: Experimental Verification 33rd Annual International Conference of the IEEE EMBS 2011
 Gamberini M., Dal Bò G., Breveglieri R., Briganti S., Passarelli L., Fattori P., Galletti C. Sensory properties of the caudal aspect of the macaque’s superior parietal lobule. Brain Structuce and Function, 2017, DOI: 10.1007/s00429-017-1593-x
 Rorie A. E., Gao J., McClelland J. L., Newsome W. T. Integration of Sensory and Reward Information during Perceptual Decision-Making in Lateral Intraparietal Cortex (LIP) of the Macaque Monkey PLoS ONE 5(2): e9308
 Gail A., Klaes C., Westendorff S. Implementation of Spatial Transformation Rules for Goal-Directed Reaching via Gain Modulation in Monkey Parietal and Premotor Cortex The Journal of Neuroscience, July 2009, 29(30):9490 –9499
 Westendorff S., Klaes C., Gail A. The Cortical Timeline for Deciding on Reach Motor Goals The Journal of Neuroscience, April 2010, 30(15):5426 –5436
 Gail A., Andersen R. A. Neural Dynamics in Monkey Parietal Reach Region Reflect Context-Specific Sensorimotor Transformations The Journal of Neuroscience, September 13, 2006, 26(37):9376 –9384
 Breveglieri R., Hadjidimitrakis K., Bosco A., Sabatini S. P., Galletti C., Fattori P. Eye Position Encoding in Three-Dimensional Space: Integration of Version and Vergence Signals in the Medial Posterior Parietal Cortex The Journal of Neuroscience, January 4, 2012 , 32(1):159 –169
 Gold J.I. , Law C., Connolly P., Bennur S. The Relative Influences of Priors and Sensory Evidence on an Oculomotor Decision Variable During Perceptual Learning J Neurophysiol, August 2008, 100:2653-2668
 Katzner S., Busse L., Treue S. Attention to the color of a moving stimulus modulates motion-signal processing in macaque area MT: evidence for a unified attentional system Frontiers in System Neurosience, October 2009, Volume 3 Article 12
 Bryant J. L., Roy S., Heck D. H. A technique for stereotaxic recordings of neuronal activity in awake, head restrained mice J Neurosci Methods, March 30; 178(1): 75-79
 Monoconduit L., Lopez-Avila A., Molat J.-L., Chalus M., Villanueva L. Corticofugal Output from the Primary Somatosensory Cortex Selectively Modulates Innocuous and Noxious Inputs in the Rat Spinothalamic System Journal of Neuroscience, Aug 2006; 26: 8441-8450
 Sundberg K.A., Fallah M., Reynolds J.H. A Motion-Dependent Distortion of Retinotopy in Area V4 Neuron 2006 49: 447-457
 Barraclough D.J., Conroy M.L. & Lee D. Prefrontal cortex and decision making in a mixed-strategy game Nature Neuroscience, Vol.7, No.4, April 2004
 Bruno R.M., Khatri V., Land P.W., Simons D.J. Thalamocortical Angular Tuning Domains within Individual Barrels of Rat Somatosensory Cortex Journal of Neuroscience, October 22, 2003, 23(29):9565-9574, 9565
 Eckhorn R., Thomas U. A new method for the insertion of multiple microprobes into neural and muscular tissue, including fiber electrdoes, fine wires, needles and microsensors Journal of Neuroscience Methods, 49 (1993) 175-179
 Mountcastle V.B., Reitboeck H.J., Poggio G.F., Steinmetz M.A. Adaptation of the Reitboeck method of multiple microelectrode recording to the neocortex of the waking monkey Journal of Neuroscience Methods, 36 (1991) 77-84