We are grateful for financial support from the European Molecular Biology Organization for a postdoctoral fellowship (to J.E.) and a grant from the NIH NHGRI (to J.J.K.). We appreciate the help of Professors Jingyue Ju and Sergey Kalachikov (Columbia University) for providing heptameric &#945;HL, and for inspiring discussions with Professor Joseph Reiner (Virginia Commonwealth University).

Note: The protocol below is specific to the Electronic BioSciences (EBS) Nanopatch DC System. However, it can be readily adapted to other electrophysiology apparatus used to measure the current through planar lipid bilayer membranes (standard lipid bilayer membrane chamber, U-tube geometry, pulled microcapillaries, etc.). The identification of commercial materials and their sources is given to describe the experimental results. In no case does this identification imply recommendation by the National Institute of Standards and Technology, nor does it imply that the materials are the best available.
1. Solution and Analyte Preparation
<ol>
	<li>Prepare all electrolyte solutions with 18 M&#937;-cm water from a Type-1 water purification system to remove trace organic species and then filter all electrolyte solutions through a 0.22 &#956;m vacuum filter immediately before ion channel recordings. 
	Note: The water quality is a critical factor for the stability and longevity of the membrane nanopore system.</li>
	<li>Wild Type &#945;HL.
	<ol>
		<li>Follow MSDS precautions when handling the &#945;HL toxin protein.</li>
		<li>Mix lyophilized wild-type monomeric S. aureus &#945;-Hemolysin (&#945;HL) powder with 18 M&#937;-cm water at 1 mg/mL. Distribute 10 to 30 &#956;L aliquots of the sample into cryo-safe centrifuge tubes, quickly flash freeze in liquid nitrogen and then store at -80 &#176;C. Alternatively, use purified preformed heptameric &#945;HL31.</li>
	</ol>
	</li>
	<li>Dissolve the lipid 1,2-Diphytanoyl-sn-Glycero-3-Phosphocholine (DPhyPC) to 0.2 mg/mL in n-decane in a 4 mL glass scintillation vial with a polytetrafluoroethyleneeflon-coated cap. Store the solution at 4 &#176;C for repeated use for up to one month.</li>
	<li>Prepare phosphotungstic acid solutions.
	<ol>
		<li>Follow MSDS precautions when handling the&#160;phosphotungstic acid&#160;powder and prepare a 2 mM phosphotungstic acid stock solution by dissolving 57.6 mg of H3PW12O40 into 10 mL of a 1 M NaCl and 10 mM NaH2PO4 solution, which constitutes the stock solution.</li>
		<li>Take 5 mL of this solution and adjust the pH to 5.5 with 3 M NaOH. Adjust the pH of the other 5 mL of the stock solution to 7.5 with 3 M NaOH. 
		Note: At pH 5.5, 12-phosphotungstic acid (PTA, H3PW12O40) decomposes primarily into the monovacant anion [PW11O39]7-.</li>
	</ol>
	</li>
</ol>
2. Test Cell Assembly
<ol>
	<li>Assemble the test cell per the manufacturer&#8217;s instructions.</li>
	<li>Soak one Ag/AgCl wire in bleach (sodium hypochlorite) for 10 minutes after abrading it with 600 grit sandpaper. Position the electrode inside the quartz nanopore membrane (QNM).</li>
	<li>Place a cylindrical AgCl pellet electrode embedded in a silver wire outside of the QNM.</li>
	<li>Once the test cell is set up, turn on the power supply and data acquisition program. Ensure that the DC current reading is 0 pA in the absence of solution in the test cell.</li>
	<li>Use a syringe connected to the test cell via a fluid line to add buffered electrolyte solution above the face of the QNM and to ensure that the ionic current saturates the amplifier. If it does not, the QNM may be clogged. Apply a pop voltage (&#177; 1 V) and/or a pressure greater than 300 mm Hg to clear it. If that works, reduce the voltage and pressure.</li>
</ol>
3. Lipid Bilayer Formation
<ol>
	<li>Fill the solution in the test cell so that the solution level is well above the face of the QNM. Then lower the solution level via syringe to below the face, such that the current decreases to zero.</li>
	<li>Dip a 10 &#956;L pipette tip into the lipid vial. Push on the back end of the pipette tip and tap it on the side of the vial to remove all visible lipid.</li>
	<li>Touch the pipette tip onto the air-water interface of the solution in the test cell when the solution level is above the QNM&#8217;s face and wait two to five minutes for the lipid to spread uniformly.</li>
	<li>Slowly lower the solution level below the face of the QNM until the current saturates, and then slowly raise the solution level past the face of the QNM to form a lipid bilayer membrane.
	<ol>
		<li>Once a bilayer appears to form (i.e., when the current goes to zero), try popping it several times by increasing the pressure and ensure that the QNM is not clogged. To reform the lipid bilayer membrane, lower the solution level below the face of the QNM and slowly raise it.</li>
	</ol>
	</li>
	<li>If the lipid bilayer membrane did not form the first time, lower the solution below the face and raise it again. If it does not form after 3 trials, add more&#160;lipids&#160;as described in 3.2 and 3.3.</li>
	<li>After forming a membrane, set the current offset to zero when the applied potential is zero.</li>
</ol>
4. &#945;HL Pore Formation
<ol>
	<li>Add 2.5 ng of purified preformed&#160;&#945;HL heptameric protein sample (or 250 ng of monomeric &#945;HL) to the test cell (volume &#8776; 200 &#956;L) to enable channel formation.</li>
	<li>Increase the pressure on the bilayer with a gas-tight syringe (Figure 1) after a bilayer is formed, to expand the membrane from the QNM, and facilitate nanopore insertion. Raise the applied back pressure typically between 40 to 200 mmHg, depending on each QNM. 
	Note: The EBS software has an automated insertion feature that applies a higher bias (typically 200 to 400 mV) to induce pore formation and then automatically reduces the desired voltage to the measurement bias once a single channel forms.</li>
	<li>After a nanopore forms, reduce the back-pressure to about 1&#8260;2 of the insertion pressure. If multiple channels are observed, remove them by significantly reducing the pressure.</li>
</ol>
5. Metallic Cluster Partitioning in the Nanopore
<ol>
	<li>To account for electrode imbalances, set the DC offset voltage such that when the applied potential is set to zero there is no measured current.</li>
	<li>Prior to adding the POM sample, perform a control experiment to ensure there are no contaminants (e.g., trace POMs from a previous experiment) in the reservoir. Specifically, acquire an ionic current trace under an applied potential of +120 mV to -120 mV in the absence of any POMs to verify that no spontaneous current blockades are present. 
	Note: Due to the asymmetric structure of the &#945;HL channel (Figure 1), the magnitute of the ionic current will differ for positive and negative applied potentials. The ratio of the measured current above this applied voltage is indicative of the orientation of the &#945;HL nanopore in the membrane.</li>
	<li>Add the POM sample by flushing the reservoir with metallic cluster solution at 1 to 5 &#956;M concentration. Alternatively, load the sample into the capillary prior to cell assembly to study the partitioning of POMs into the other end of the &#945;HL channel.</li>
	<li>Record the ionic current using the manufacturer&#8217;s software to detect transient current blockades caused by partitioning of individual POMs into the nanopore. Estimate the physical and chemical properties of the molecule from the ionic current blockade depth, event frequency, and the residence time distribution of the blockades.</li>
</ol>
6. Ion Channel Recordings and Data Analysis
<ol>
	<li>Acquire the ionic current time series measurements using a high-impedance, low-noise amplifier and data acquisition system. Perform the measurements at an applied voltage of -120 mV (relative to channel cis side) for each pH.</li>
	<li>Apply a low-pass 100 kHz 8-pole Bessel filter to the signal, which is subsequently digitized at 500 kHz (i.e., 2 &#956;s/point). Extract events from the time series and analyze events using the ADEPT algorithm in the MOSAIC software package32,33.</li>
</ol>

<ol>
	<li>Ettedgui, J., Kasianowicz, J. J., Balijepalli, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Single+molecule+discrimination+of+heteropolytungstates+and+their+Isomers+in+solution+with+a+nanometer-scale+pore.">Single molecule discrimination of heteropolytungstates and their Isomers in solution with a nanometer-scale pore.</a> Journal of the American Chemical Society. 138 (23), 7228-7231 (2016).</li><li>Bezrukov, S., Kasianowicz, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Current+noise+reveals+protonation+kinetics+and+number+of+ionizable+sites+in+an+open+protein+ion+channel.">Current noise reveals protonation kinetics and number of ionizable sites in an open protein ion channel.</a> Physical Review Letters. 70 (15), 2352-2355 (1993).</li><li>Kasianowicz, J. J., Bezrukov, S. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Protonation+dynamics+of+the+alpha-toxin+ion+channel+from+spectral+analysis+of+pH-dependent+current+fluctuations.">Protonation dynamics of the alpha-toxin ion channel from spectral analysis of pH-dependent current fluctuations.</a> Biophysj. 69 (1), 94-105 (1995).</li><li>Please, T. R., Ayub, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Solid-State+Nanopore.">Solid-State Nanopore.</a> Engineered Nanopores for Bioanalytical Applications. , 121-140 (2013).</li><li>Dekker, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Solid-state+nanopores.">Solid-state nanopores.</a> Nature Nanotechnology. 2 (4), 209-215 (2007).</li><li>Kasianowicz, J. J., Brandin, E., Branton, D., Deamer, D. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Characterization+of+individual+polynucleotide+molecules+using+a+membrane+channel.">Characterization of individual polynucleotide molecules using a membrane channel.</a> Proceedings of the National Academy of Sciences of the United States of America. 93 (24), 13770-13773 (1996).</li><li>Akeson, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microsecond+time-scale+discrimination+among+polycytidylic+acid,+polyadenylic+acid,+and+polyuridylic+acid+as+homopolymers+or+as+segments+within+single+RNA+molecules.">Microsecond time-scale discrimination among polycytidylic acid, polyadenylic acid, and polyuridylic acid as homopolymers or as segments within single RNA molecules.</a> Biophysical Journal. 77 (6), 3227-3233 (1999).</li><li>Singer, A., Meller, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nanopore-based+Sensing+of+Individual+Nucleic+Acid+Complexes.">Nanopore-based Sensing of Individual Nucleic Acid Complexes.</a> Israel Journal of Chemistry. 49 (3-4), 323-331 (2010).</li><li>Jin, Q., Fleming, A. M., Burrows, C. J., White, H. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Unzipping+kinetics+of+duplex+DNA+containing+oxidized+lesions+in+an+&#945;-hemolysin+nanopore.">Unzipping kinetics of duplex DNA containing oxidized lesions in an &#945;-hemolysin nanopore.</a> Journal of the American Chemical Society. 134 (26), 11006-11011 (2012).</li><li>Halverson, K. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Anthrax+biosensor,+protective+antigen+ion+channel+asymmetric+blockade.">Anthrax biosensor, protective antigen ion channel asymmetric blockade.</a> Journal of Biological Chemistry. 280 (40), 34056-34062 (2005).</li><li>Oukhaled, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Unfolding+of+proteins+and+long+transient+conformations+detected+by+single+nanopore+recording.">Unfolding of proteins and long transient conformations detected by single nanopore recording.</a> Physical Review Letters. 98 (15), 158101 (2007).</li><li>Reiner, J. E., Kasianowicz, J. J., Nablo, B. J., Robertson, J. W. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Theory+for+polymer+analysis+using+nanopore-based+single-molecule+mass+spectrometry.">Theory for polymer analysis using nanopore-based single-molecule mass spectrometry.</a> Proceedings of the National Academy of Sciences of the United States of America. 107 (27), 12080-12085 (2010).</li><li>Robertson, J. W. F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Single-molecule+mass+spectrometry+in+solution+using+a+solitary+nanopore.">Single-molecule mass spectrometry in solution using a solitary nanopore.</a> Proceedings of the National Academy of Sciences of the United States of America. 104 (20), 8207-8211 (2007).</li><li>Baaken, G., Ankri, N., Schuler, A. -. K., R&#252;he, J., Behrends, J. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nanopore-based+single-molecule+mass+spectrometry+on+a+lipid+membrane+microarray.">Nanopore-based single-molecule mass spectrometry on a lipid membrane microarray.</a> ACS Nano. 5 (10), 8080-8088 (2011).</li><li>Angevine, C. E., Chavis, A. E., Kothalawala, N., Dass, A., Reiner, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enhanced+single+molecule+mass+spectrometry+via+charged+metallic+clusters.">Enhanced single molecule mass spectrometry via charged metallic clusters.</a> Analytical Chemistry. 86 (22), 11077-11085 (2014).</li><li>Astier, Y., Uzun, O., Stellacci, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Electrophysiological+study+of+single+gold+nanoparticle/alpha-Hemolysin+complex+formation:+a+nanotool+to+slow+down+ssDNA+through+the+alpha-Hemolysin+nanopore.">Electrophysiological study of single gold nanoparticle/alpha-Hemolysin complex formation: a nanotool to slow down ssDNA through the alpha-Hemolysin nanopore.</a> Small. 5 (11), 1273-1278 (2009).</li><li>Chavis, A. E., Brady, K. T., Kothalawala, N., Reiner, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Voltage+and+blockade+state+optimization+of+cluster-enhanced+nanopore+spectrometry.">Voltage and blockade state optimization of cluster-enhanced nanopore spectrometry.</a> Analyst. 140 (22), 7718-7725 (2015).</li><li>Campos, E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sensing+single+mixed-monolayer+protected+gold+nanoparticles+by+the+&#945;-hemolysin+nanopore.">Sensing single mixed-monolayer protected gold nanoparticles by the &#945;-hemolysin nanopore.</a> Analytical Chemistry. 85 (21), 10149-10158 (2013).</li><li>Campos, E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+role+of+Lys147+in+the+interaction+between+MPSA-gold+nanoparticles+and+the+&#945;-hemolysin+nanopore.">The role of Lys147 in the interaction between MPSA-gold nanoparticles and the &#945;-hemolysin nanopore.</a> Langmuir. 28 (44), 15643-15650 (2012).</li><li>Baaken, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High-Resolution+Size-Discrimination+of+Single+Nonionic+Synthetic+Polymers+with+a+Highly+Charged+Biological+Nanopore.">High-Resolution Size-Discrimination of Single Nonionic Synthetic Polymers with a Highly Charged Biological Nanopore.</a> ACS Nano. 9 (6), 6443-6449 (2015).</li><li>Berzelius, J. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Beitrag+zur+n&#228;heren+Kenntniss+des+Molybd&#228;ns.">Beitrag zur n&#228;heren Kenntniss des Molybd&#228;ns.</a> Annalen Der Physik. 82 (1), 369-392 (1826).</li><li>Long, D. -. L., Burkholder, E., Cronin, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polyoxometalate+clusters,+nanostructures+and+materials:+from+self+assembly+to+designer+materials+and+devices.">Polyoxometalate clusters, nanostructures and materials: from self assembly to designer materials and devices.</a> Chemical Society Reviews. 36 (1), 105-121 (2007).</li><li>Muller, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polyoxovanadates:+High-nuclearity+spin+clusters+with+interesting+host-guest+systems+and+different+electron+populations.+Synthesis,+spin+organization,+magnetochemistry,+and+spectroscopic+studies.">Polyoxovanadates: High-nuclearity spin clusters with interesting host-guest systems and different electron populations. Synthesis, spin organization, magnetochemistry, and spectroscopic studies.</a> Inorganic Chemistry. 36 (23), 5239-5250 (1997).</li><li>Rausch, B., Symes, M. D., Chisholm, G., Cronin, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Decoupled+catalytic+hydrogen+evolution+from+a+molecular+metal+oxide+redox+mediator+in+water+splitting.">Decoupled catalytic hydrogen evolution from a molecular metal oxide redox mediator in water splitting.</a> Science. 345 (6202), 1326-1330 (2014).</li><li>Dolbecq, A., Dumas, E., Mayer, C. R., Mialane, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hybrid+organic-inorganic+polyoxometalate+compounds:+from+structural+diversity+to+applications.">Hybrid organic-inorganic polyoxometalate compounds: from structural diversity to applications.</a> Chemical Reviews. 110 (10), 6009-6048 (2010).</li><li>Busche, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Design+and+fabrication+of+memory+devices+based+on+nanoscale+polyoxometalate+clusters.">Design and fabrication of memory devices based on nanoscale polyoxometalate clusters.</a> Nature. 515 (7528), 545-549 (2014).</li><li>Pope, M., M&#252;ller, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Polyoxometalates: From Platonic Solids to Anti-Retroviral Activity. 10, (2012).</li><li>Rhule, J. T., Hill, C. L., Judd, D. A., Schinazi, R. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polyoxometalates+in+medicine.">Polyoxometalates in medicine.</a> Chemical Reviews. 98 (1), 327-358 (1998).</li><li>Gao, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transition-metal-substituted+polyoxometalate+derivatives+as+functional+anti-amyloid+agents+for+Alzheimer's+disease.">Transition-metal-substituted polyoxometalate derivatives as functional anti-amyloid agents for Alzheimer's disease.</a> Nature Communications. 5, 3422 (2014).</li><li>Pope, M. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Heteropoly and Isopoly Oxometalates. 8, (1983).</li><li>Braha, O., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Designed+protein+pores+as+components+for+biosensors.">Designed protein pores as components for biosensors.</a> Chemistry &amp; Biology. 4 (7), 497-505 (1997).</li><li>Forstater, J. H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=MOSAIC:+A+modular+single-molecule+analysis+interface+for+decoding+multistate+nanopore+data.">MOSAIC: A modular single-molecule analysis interface for decoding multistate nanopore data.</a> Analytical Chemistry. 88 (23), 11900-11907 (2016).</li><li>Balijepalli, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantifying+Short-Lived+Events+in+Multistate+Ionic+Current+Measurements.">Quantifying Short-Lived Events in Multistate Ionic Current Measurements.</a> ACS Nano. 8, 1547-1553 (2014).</li><li>Misakian, M. M., Kasianowicz, J. J. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Electrostatic+influence+on+ion+transport+through+the+alphaHL+channel.">Electrostatic influence on ion transport through the alphaHL channel.</a> Journal of Membrane Biology. 195 (3), 137-146 (2003).</li><li>Piguet, F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Identification+of+single+amino+acid+differences+in+uniformly+charged+homopolymeric+peptides+with+aerolysin+nanopore.">Identification of single amino acid differences in uniformly charged homopolymeric peptides with aerolysin nanopore.</a> Nature Communication. 9 (966), (2018).</li></ol>

Due to their anionic charge, POMs likely associate with organic counter cations through electrostatic interactions. Therefore, it is important to identify the proper solution conditions and the right electrolyte environments (especially cations in solution) to avoid complex formation with POMs. Particular care is required in the buffer choice. For example, the capture rate of POMs with tris(hydroxymethyl)aminomethane and citric acid-buffered solutions is significantly lower than that in phosphate buffered solution, likel...

Detecting biomolecular analytes at the single molecule level can be performed by using nanopores and measuring ionic current modulations. Typically, nanopores are divided into two categories based on their fabrication: biological (self-assembled from protein or DNA origami)1,2,3, or solid-state (e.g., manufactured with semiconductor processing tools)4,5. While solid-state nanopores were suggested as potentially more physically robust and can be used over a wide range of solution conditions, protein nanopores thus far offer greater sensitivity, more resistance to fouling, greater bandwidth, better chemical selectivity, and a greater signal to noise ratio.
A variety of protein ion channels, such as the one formed by Staphylococcus aureus &#945;-hemolysin (&#945;HL), can be used to detect single molecules, including ions (e.g., H+ and D+)2,3, polynucleotides (DNA and RNA)6,7,8, damaged DNA9, polypeptides10, proteins (folded and unfolded)11, polymers (polyethylene glycol and others)12,13,14, gold nanoparticles15,16,17,18,19, and other synthetic molecules20.
We recently demonstrated that the &#945;HL nanopore can also easily detect and characterize metallic clusters, polyoxometalates (POMs), at the single molecule level. POMs are discrete nanoscale anionic metal oxygen clusters that were discovered in 182621, and since then, many more types have been synthesized. The different sizes, structures, and elemental compositions of polyoxometalates that are now available led to a wide range of properties and applications including chemistry22,23, catalysis24, material science25,26, and biomedical research27,28,29.
POM synthesis is a self-assembly process typically carried out in water by mixing the stoichiometrically required amounts of monomeric metal salts. Once formed, POMs exhibit a great diversity of sizes and shapes. For example, the Keggin polyanion structure, XM12O40q- is composed of one heteroatom (X) surrounded by four oxygens to form a tetrahedron (q is the charge). The heteroatom is centrally located within a cage formed by 12 octahedral MO6 units (where M = transition metals in their high oxidation state), which are linked to one another by neighboring shared oxygen atoms. While tungsten polyoxometalates structure is stable in acidic conditions, hydroxide ions lead to the hydrolytic cleavage of metal-oxygen (M-O) bonds30. This complex process results in the loss of one or more MO6 octahedral subunits, leading to the formation of monovacant and trivacant species and eventually to the complete decomposition of the POMs. Our discussion here will be limited to the partial decomposition products of 12-phosphotungstic acid at pH 5.5 and 7.5.
The goal of this protocol is to detect discrete metal oxygen clusters at the single molecule limit using a biological nanopore-based electronic platform. This method allows the detection of metallic clusters in solution. Multiple species in solution can be discriminated with greater sensitivity than conventional analytical methods33. With it, subtle differences in POM structure can be elucidated, and at concentrations markedly lower than those required for NMR spectroscopy. Importantly, this approach even allows the discrimination of isomeric forms of Na8HPW9O341.

<table>
	<tbody>
		<tr>
			<td>Nanopatch DC System</td>
			<td>Electronic Biosciences, Inc., EBS</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Millipore LC-PAK</td>
			<td>Millipore vacuum filter</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>1,2-Diphytanoyl-sn- Glycero-3-Phosphocholine (DPhPC)</td>
			<td>Avanti Polar Lipids, Alabaster, AL</td>
			<td>850356P</td>
			<td></td>
		</tr>
		<tr>
			<td>Decane, ReagentPlus, &#8805;99%,</td>
			<td>Sigma-Aldrich</td>
			<td>D901</td>
			<td></td>
		</tr>
		<tr>
			<td>&#945;HL</td>
			<td>List Biological Laboratories, Campbell, CA</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Ag wire</td>
			<td>Alfa Aesar</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>2 mm Ag/AgCl disk electrode</td>
			<td>In Vivo Metric</td>
			<td>E202</td>
			<td></td>
		</tr>
		<tr>
			<td>High-impedance amplifier system</td>
			<td>Electronic Biosciences, San Diego, CA</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>quartz capillaries</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>custom polycarbonate test cell</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Data Processing and Analysis MOSAIC</td>
			<td>https://pages.nist.gov/mosaic/</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Phosphotungstic acid hydrate</td>
			<td>Sigma-Aldrich</td>
			<td>455970</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium Chloride</td>
			<td>Sigma-Aldrich</td>
			<td>S3014</td>
			<td></td>
		</tr>
		<tr>
			<td>sodium phosphate monobasic monohydrate</td>
			<td>Sigma-Aldrich</td>
			<td>71507</td>
			<td></td>
		</tr>
	</tbody>
</table>

high resolution physical characterization of single metallic nanoparticles

Individual molecules can be detected and characterized by measuring the degree by which they reduce the ionic current flowing through a single nanometer-scale pore. The signal is characteristic of the molecule&#39;s physicochemical properties and its interactions with the pore. We demonstrate that the nanopore formed by the bacterial protein exotoxin Staphylococcus aureus alpha hemolysin (&#945;HL) can detect polyoxometalates (POMs, anionic metal oxygen clusters), at the single molecule limit. Moreover, multiple degradation products of 12-phosphotungstic acid POM (PTA, H3PW12O40) in solution are simultaneously measured. The single molecule sensitivity of the nanopore method allows for POMs to be characterized at significantly lower concentrations than required for nuclear magnetic resonance (NMR) spectroscopy. This technique could serve as a new tool for chemists to study the molecular properties of polyoxometalates or other metallic clusters, to better understand POM synthetic processes, and possibly improve their yield. Hypothetically, the location of a given atom, or the rotation of a fragment in the molecule, and the metal oxidation state could be investigated with this method. In addition, this new technique has the advantage of allowing the real-time monitoring of molecules in solution.&#160;

Over the past two decades, membrane-bound protein nanometer-scale pores have been demonstrated as versatile single-molecule sensors. Nanopore-based measurements are relatively straightforward to execute.&#160; Two chambers&#160;filled with electrolyte solution are separated by a nanopore embedded in an electrically insulating lipid membrane. Either a patch-clamp amplifier or an external power supply provides an electrostatic potential across the nanopore via Ag/AgCl electrodes im...

Watch this Scientific Journal Video about High Resolution Physical Characterization of Single Metallic Nanoparticles at JoVE.com

High Resolution Physical Characterization of Single Metallic Nanoparticles

Here, we present a protocol to detect discrete metal oxygen clusters, polyoxometalates (POMs), at the single molecule limit using a biological nanopore-based electronic platform. The method provides a complementary approach to traditional analytical chemistry tools used in the study of these molecules.

Individual molecules can be detected and characterized by measuring the degree by which they reduce the ionic current flowing through a single ...

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Chemistry

5.7K Views.  National Institute of Standards and Technology. Here, we present a protocol to detect discrete metal oxygen clusters, polyoxometalates (POMs), at the single molecule limit using a biological nanopore-based electronic platform. The method provides a complementary approach to traditional analytical chemistry tools used in the study of these molecules.

Video: High Resolution Physical Characterization of Single Metallic Nanoparticles

Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry (UPLC-HRMS)

Here we present a workflow to analyze the metabolic profiles for biological samples of interest including; cells, serum, or tissue. The sample is first separated into polar and non-polar fractions by a liquid-liquid phase extraction, and partially purified to facilitate downstream analysis. Both aqueous (polar metabolites) and organic (non-polar metabolites) phases of the initial extraction are processed to survey a broad range of metabolites. Metabolites are separated by different liquid chromatography methods based upon their partition properties. In this method, we present microflow ultra-performance (UP)LC methods, but the protocol is scalable to higher flows and lower pressures. Introduction into the mass spectrometer can be through either general or compound optimized source conditions. Detection of a broad range of ions is carried out in full scan mode in both positive and negative mode over a broad m/z range using high resolution on a recently calibrated instrument. Label-free differential analysis is carried out on bioinformatics platforms. Applications of this approach include metabolic pathway screening, biomarker discovery, and drug development.

Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry UPLC-HRMS

Untargeted metabolomics provides a hypothesis generating snapshot of a metabolic profile. This protocol will demonstrate the extraction and analysis of metabolites from cells, serum, or tissue. A range of metabolites are surveyed using liquid-liquid phase extraction, microflow ultraperformance liquid chromatography/high-resolution mass spectrometry (UPLC-HRMS) coupled to differential analysis software.

Here we present a workflow to analyze the metabolic profiles for biological samples of interest including; cells, serum, or tissue. The sample is first ...

Preparation and Characterization of SDF-1&#945;-Chitosan-Dextran Sulfate Nanoparticles

Chitosan (CS) and dextran sulfate (DS) are charged polysaccharides (glycans), which form polyelectrolyte complex-based nanoparticles when mixed under appropriate conditions. The glycan nanoparticles are useful carriers for protein factors, which facilitate the in vivo delivery of the proteins and sustain their retention in the targeted tissue. The glycan polyelectrolyte complexes are also ideal for protein delivery, as the incorporation is carried out in aqueous solution, which reduces the likelihood of inactivation of the proteins. Proteins with a heparin-binding site adhere to dextran sulfate readily, and are, in turn, stabilized by the binding. These particles are also less inflammatory and toxic when delivered in vivo. In the protocol described below, SDF-1&#945; (Stromal cell-derived factor-1&#945;), a stem cell homing factor, is first mixed and incubated with dextran sulfate. Chitosan is added to the mixture to form polyelectrolyte complexes, followed by zinc sulfate to stabilize the complexes with zinc bridges. The resultant SDF-1&#945;-DS-CS particles are measured for size (diameter) and surface charge (zeta potential). The amount of the incorporated SDF-1&#945; is determined, followed by measurements of its in vitro release rate and its chemotactic activity in a particle-bound form.

The objective of this protocol is to incorporate SDF-1&#945;, a stem cell homing factor, into dextran sulfate-chitosan nanoparticles. The resultant particles are measured for their size and zeta potential, as well as the content, activity, and in vitro release rate of SDF-1&#945; from the nanoparticles.

Chitosan (CS) and dextran sulfate (DS) are charged polysaccharides (glycans), which form polyelectrolyte complex-based nanoparticles when mixed under ...

Synthesis, Characterization, and Functionalization of Hybrid Au/CdS and Au/ZnS Core/Shell Nanoparticles

Plasmonic nanoparticles are an attractive material for light harvesting applications due to their easily modified surface, high surface area and large extinction coefficients which can be tuned across the visible spectrum. Research into the plasmonic enhancement of optical transitions has become popular, due to the possibility of altering and in some cases improving photo-absorption or emission properties of nearby chromophores such as molecular dyes or quantum dots. The electric field of the plasmon can couple with the excitation dipole of a chromophore, perturbing the electronic states involved in the transition and leading to increased absorption and emission rates. These enhancements can also be negated at close distances by energy transfer mechanism, making the spatial arrangement of the two species critical. Ultimately, enhancement of light harvesting efficiency in plasmonic solar cells could lead to thinner and, therefore, lower cost devices. The development of hybrid core/shell particles could offer a solution to this issue. The addition of a dielectric spacer between a gold nanoparticles and a chromophore is the proposed method to control the exciton plasmon coupling strength and thereby balance losses with the plasmonic gains. A detailed procedure for the coating of gold nanoparticles with CdS and ZnS semiconductor shells is presented. The nanoparticles show high uniformity with size control in both the core gold particles and shell species allowing for a more accurate investigation into the plasmonic enhancement of external chromophores.

The synthesis of uniform gold nanoparticles coated with semiconductor shells of CdS or ZnS is performed. The semiconductor coating is conducted by first depositing a silver sulfide shell and exchanging the silver cations for zinc or cadmium cations.

Plasmonic nanoparticles are an attractive material for light harvesting applications due to their easily modified surface, high surface area and large ...

Synthesis and Characterization of Supramolecular Colloids

Control over colloidal assembly is of utmost importance for the development of functional colloidal materials with tailored structural and mechanical properties for applications in photonics, drug delivery and coating technology. Here we present a new family of colloidal building blocks, coined supramolecular colloids, whose self-assembly is controlled through surface-functionalization with a benzene-1,3,5-tricarboxamide (BTA) derived supramolecular moiety. Such BTAs interact via directional, strong, yet reversible hydrogen-bonds with other identical BTAs. Herein, a protocol is presented that describes how to couple these BTAs to colloids and how to quantify the number of coupling sites, which determines the multivalency of the supramolecular colloids. Light scattering measurements show that the refractive index of the colloids is almost matched with that of the solvent, which strongly reduces the van der Waals forces between the colloids. Before photo-activation, the colloids remain well dispersed, as the BTAs are equipped with a photo-labile group that blocks the formation of hydrogen-bonds. Controlled deprotection with UV-light activates the short-range hydrogen-bonds between the BTAs, which triggers the colloidal self-assembly. The evolution from the dispersed state to the clustered state is monitored by confocal microscopy. These results are further quantified by image analysis with simple routines using ImageJ and Matlab. This merger of supramolecular chemistry and colloidal science offers a direct route towards light- and thermo-responsive colloidal assembly encoded in the surface-grafted monolayer.

A protocol for the synthesis and characterization of colloids coated with supramolecular moieties is described. These supramolecular colloids undergo self-assembly upon the activation of the hydrogen-bonds between the surface-anchored molecules by UV-light.

Control over colloidal assembly is of utmost importance for the development of functional colloidal materials with tailored structural and mechanical ...

Rapid High-throughput Species Identification of Botanical Material Using Direct Analysis in Real Time High Resolution Mass Spectrometry

We demonstrate that direct analysis in real time-high resolution mass spectrometry can be used to produce mass spectral profiles of botanical material, and that these chemical fingerprints can be used for plant species identification. The mass spectral data can be acquired rapidly and in a high throughput manner without the need for sample extraction, derivatization or pH adjustment steps. The use of this technique bypasses challenges presented by more conventional techniques including lengthy chromatography analysis times and resource intensive methods. The high throughput capabilities of the direct analysis in real time-high resolution mass spectrometry protocol, coupled with multivariate statistical analysis processing of the data, provide not only class characterization of plants, but also yield species and varietal information. Here, the technique is demonstrated with two psychoactive plant products, Mitragyna speciosa (Kratom) and Datura (Jimsonweed), which were subjected to direct analysis in real time-high resolution mass spectrometry followed by statistical analysis processing of the mass spectral data. The application of these tools in tandem enabled the plant materials to be rapidly identified at the level of variety and species.

A method for species identification of botanical material by direct analysis in real time-high resolution mass spectrometry and multivariate statistical analysis is presented.

We demonstrate that direct analysis in real time-high resolution mass spectrometry can be used to produce mass spectral profiles of botanical material, ...

High Pressure Single Crystal Diffraction at PX^2

In this report we describe detailed procedures for carrying out single crystal X-ray diffraction experiments with a diamond anvil cell (DAC) at the GSECARS 13-BM-C beamline at the Advanced Photon Source. The DAC program at 13-BM-C is part of the Partnership for Extreme Xtallography (PX^2) project. BX-90 type DACs with conical-type diamond anvils and backing plates are recommended for these experiments. The sample chamber should be loaded with noble gas to maintain a hydrostatic pressure environment. The sample is aligned to the rotation center of the diffraction goniometer. The MARCCD area detector is calibrated with a powder diffraction pattern from LaB6. The sample diffraction peaks are analyzed with the ATREX software program, and are then indexed with the RSV software program. RSV is used to refine the UB matrix of the single crystal, and with this information and the peak prediction function, more diffraction peaks can be located. Representative single crystal diffraction data from an omphacite (Ca0.51Na0.48)(Mg0.44Al0.44Fe2+0.14Fe3+0.02)Si2O6 sample were collected. Analysis of the data gave a monoclinic lattice with P2/n space group at 0.35 GPa, and the lattice parameters were found to be: a = 9.496 &#177;0.006 &#197;, b = 8.761 &#177;0.004 &#197;, c = 5.248 &#177;0.001 &#197;, &#946; = 105.06 &#177;0.03&#186;, &#945; = &#947; = 90&#186;.

In this report, we describe detailed procedures for carrying out single crystal X-ray diffraction experiments with a diamond anvil cell at the GSECARS 13-BM-C beamline at the Advanced Photon Source. ATREX and RSV programs are used to analyze the data.

In this report we describe detailed procedures for carrying out single crystal X-ray diffraction experiments with a diamond anvil cell (DAC) at the ...

In Situ Detection and Single Cell Quantification of Metal Oxide Nanoparticles Using Nuclear Microprobe Analysis

Micro-analytical techniques based on chemical element imaging enable the localization and quantification of chemical composition at the cellular level. They offer new possibilities for the characterization of living systems and are particularly appropriate for detecting, localizing and quantifying the presence of metal oxide nanoparticles both in biological specimens and the environment. Indeed, these techniques all meet relevant requirements in terms of (i) sensitivity (from 1 up to 10 &#181;g.g-1 of dry mass), (ii) micrometer range spatial resolution, and (iii) multi-element detection. Given these characteristics, microbeam chemical element imaging can powerfully complement routine imaging techniques such as optical and fluorescence microscopy. This protocol describes how to perform a nuclear microprobe analysis on cultured cells (U2OS) exposed to titanium dioxide nanoparticles. Cells must grow on and be exposed directly in a specially designed sample holder used on the optical microscope and in the nuclear microprobe analysis stages. Plunge-freeze cryogenic fixation of the samples preserves both the cellular organization and the chemical element distribution. Simultaneous nuclear microprobe analysis (scanning transmission ion microscopy, Rutherford backscattering spectrometry and particle induced X-ray emission) performed on the sample provides information about the cellular density, the local distribution of the chemical elements, as well as the cellular content of nanoparticles. There is a growing need for such analytical tools within biology, especially in the emerging context of Nanotoxicology and Nanomedicine for which our comprehension of the interactions between nanoparticles and biological samples must be deepened. In particular, as nuclear microprobe analysis does not require nanoparticles to be labelled, nanoparticle abundances are quantifiable down to the individual cell level in a cell population, independently of their surface state.

In Situ Detection and Single Cell Quantification of Metal Oxide Nanoparticles Using Nuclear Microprobe Analysis

We describe a procedure for the detection of chemical elements present in situ in human cells as well as their in vitro quantification. The method is well-suited to any cell type and is particularly useful for quantitative chemical analyses in single cells following in vitro metal oxide nanoparticles exposure.

Micro-analytical techniques based on chemical element imaging enable the localization and quantification of chemical composition at the cellular level. ...

Real-time Breath Analysis by Using Secondary Nanoelectrospray Ionization Coupled to High Resolution Mass Spectrometry

Exhaled volatile organic compounds (VOCs) have aroused considerable interest, since they can serve as biomarkers for disease diagnosis and environmental exposure in a non-invasive manner. In this work, we present a protocol to characterize the exhaled VOCs in real time by using secondary nanoelectrospray ionization coupled to high resolution mass spectrometry (Sec-nanoESI-HRMS). The homemade Sec-nanoESI source was readily set up based on a commercial nanoESI source. Hundreds of peaks were observed in the background-subtracted mass spectra of exhaled breath, and the mass accuracy values are -4.0-13.5 ppm and -20.3-1.3 ppm in the positive and negative ion detection modes, respectively. The peaks were assigned with accurate elemental composition according to the accurate mass and isotopic pattern. Less than 30 s is used for one exhalation measurement, and it takes approximately 7 min for six replicated measurements.

A protocol for characterizing chemical composition of exhaled breath in real time by using secondary nanoelectrospray ionization coupled to high resolution mass spectrometry is demonstrated.

Exhaled volatile organic compounds (VOCs) have aroused considerable interest, since they can serve as biomarkers for disease diagnosis and environmental ...

Synthesis and Characterization of Amphiphilic Gold Nanoparticles

Gold nanoparticles covered with a mixture of 1-octanethiol (OT) and 11-mercapto-1-undecane sulfonic acid (MUS) have been extensively studied because of their interactions with cell membranes, lipid bilayers, and viruses. The hydrophilic ligands make these particles colloidally stable in aqueous solutions and the combination with hydrophobic ligands creates an amphiphilic particle that can be loaded with hydrophobic drugs, fuse with the lipid membranes, and resist nonspecific protein adsorption. Many of these properties depend on nanoparticle size and the composition of the ligand shell. It is, therefore, crucial to have a reproducible synthetic method and reliable characterization techniques that allow the determination of nanoparticle properties and the ligand shell composition. Here, a one-phase chemical reduction, followed by a thorough purification to synthesize these nanoparticles with diameters below 5 nm, is presented. The ratio between the two ligands on the surface of the nanoparticle can be tuned through their stoichiometric ratio used during synthesis. We demonstrate how various routine techniques, such as transmission electron microscopy (TEM), nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), and ultraviolet-visible (UV-Vis) spectrometry, are combined to comprehensively characterize the physicochemical parameters of the nanoparticles.

Amphiphilic gold nanoparticles can be used in many biological applications. A protocol to synthesize gold nanoparticles coated by a binary mixture of ligands and a detailed characterization of these particles is presented.

Gold nanoparticles covered with a mixture of 1-octanethiol (OT) and 11-mercapto-1-undecane sulfonic acid (MUS) have been extensively studied because of ...

A Continuous-flow Photocatalytic Reactor for the Precisely Controlled Deposition of Metallic Nanoparticles

In this work, a novel photocatalytic reactor for the pulsed and controlled excitation of the photocatalyst and the precise deposition of metallic nanoparticles is developed. Guidelines for the replication of the reactor and its operation are provided in detail. Three different composite systems (Pt/graphene, Pt/TiO2, and Au/TiO2) with monodisperse and uniformly distributed particles are produced by this reactor, and the photodeposition mechanism, as well as the synthesis optimization strategy, are discussed. The synthesis methods and their technical aspects are described comprehensively. The role of the ultraviolet (UV) dose (in each excitation pulse) on the photodeposition process is investigated and the optimum values for each composite system are provided.

For a continuous and scalable synthesis of noble-metal-based nanocomposites, a novel photocatalytic reactor is developed and its structure, operation principles, and product quality optimization strategies are described.

High Resolution Physical Characterization of Single Metallic Nanoparticles

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Rozdziały w tym wideo

Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry (UPLC-HRMS)

Preparation and Characterization of SDF-1α-Chitosan-Dextran Sulfate Nanoparticles

Synthesis, Characterization, and Functionalization of Hybrid Au/CdS and Au/ZnS Core/Shell Nanoparticles

Synthesis and Characterization of Supramolecular Colloids

Rapid High-throughput Species Identification of Botanical Material Using Direct Analysis in Real Time High Resolution Mass Spectrometry

High Pressure Single Crystal Diffraction at PX^2

In Situ Detection and Single Cell Quantification of Metal Oxide Nanoparticles Using Nuclear Microprobe Analysis

Real-time Breath Analysis by Using Secondary Nanoelectrospray Ionization Coupled to High Resolution Mass Spectrometry

Synthesis and Characterization of Amphiphilic Gold Nanoparticles

A Continuous-flow Photocatalytic Reactor for the Precisely Controlled Deposition of Metallic Nanoparticles