This work received support through grant HA 6136/1-1 from the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) to MH. JAT is supported by Program and Project Grants from the National Health and Medical Research Council of Australia.

HINWEIS: Die Milz wurde aus Mäusen (6-10 Wochen alt) und alle Tierversuche wurden nach den Tierethik Richtlinien der Peter MacCallum Cancer Center (E486) durchgeführt. 1. Vorbereitung der Proben. <ol><li> Herstellung von aktivierten Maus-NK-Zellen. <ol><li> Isolieren Primär naive NK-Zellen von Einzelzellsuspensionen von den Milzen von C57BL / 6 oder B6.GrzmB - / - (GzmB Gen null) Mäusen durch negative Selektion unter Verwendung von kommerziell erhältlichen Kits. </li><li> Folgen Protokoll der Hersteller. Kurz gesagt, magnetisch zu markieren &quot;nicht-NK&quot; Zellen, wie T- und B-Zellen, dendritischen Zellen, Granulozyten, Makrophagen und Erythrozyten unter Verwendung von Biotin-konjugiertem Antikörper gegen ihre spezifischen Oberflächenmarkern. Verwenden magnetischer Trennung mit Anti-Biotin-Perlen zu &quot;nicht-NK&quot; Zellen abzureichern. </li><li> Kultur isoliert NK-Zellen für 5-7 Tage in Medium, das IL-2 (1.000 U / ml) bei 700000 Zellen / ml in 24-Well-Plattenbei 37 &#160; ° C. </li><li> Alternativ aktiviert Verwendung T-Zellen 19, primäre Antigen-restringierte CTL aus OT1 T-Zell-Rezeptor-transgenen Mäusen 20 erzeugte CTL in gemischten Lymphozyten-Kulturen 21 oder Überständen von aktivierten NK-Zellen, um die Aktivität der sekretierten GzmB 19 bestimmen. </li></ol></li><li> Wartung der menschlichen NK-Zelllinie und Isolierung von primären NK-Zellen. <ol><li> Pflege der menschlichen NK Leukämie (YT-Zellen) in Roswell Park Memorial Institute (RPMI) Medium mit 10% fötalem Kälberserum ergänzt. Alternativ reinigen primären NK-Zellen aus dem peripheren Blut von gesunden Probanden und für 2-3 Tage in einem Medium anzuregen, das IL-2 bei 100 U / ml, wie zuvor beschrieben 22. </li></ol></li><li> Erzeugung von Zelllysaten. <ol><li> Wash-Zellen dreimal in PBS (pH 7,4), dann in Nonidet P-40 Lysepuffer auszusetzen (0,1% NP-40, 250 mM NaCl, 25 mM Hepes, 2,5 mM EDTA). Idealerweise Lyse von mindestens 5 x 10 6 </sbis&gt; NK-Zellen oder 1 · 10 7 T-Zellen in 100 ul Puffer. Nicht hinzufügen Proteaseinhibitoren, wie viele sind irreversible Inhibitoren von Serinproteasen, insbesondere Tryptasen wie GZMA. Inkubieren auf Eis für 20 min, und dann die Kerne zu pelletieren in einer Mikrozentrifuge bei 15.000 × g für 10 min. Entsorgen Sie die Kernpellet und den Überstand in ein frisches Röhrchen. </li></ol></li><li> Bestimmung der Proteinkonzentration der Lysate. <ol><li> Verwenden Sie ein handelsübliches Protokoll der Wahl, wie Bradford oder Bicinchoninsäure (BCA) und bestimmen Sie die Proteinkonzentration. Sicherzustellen, dass die Konzentration von ~ 2 mg / ml Minimum. Speicher Lysate bei -20 ° C bis zur Verwendung (Granzym-Aktivität ist für viele Monate bei -20 ° C stabil). </li></ol></li></ol> 2. Granzyme B-Aktivitätstest <ol><li> Herstellung der Reagenzien <ol><li> Bereiten Sie eine 10 mM Stamm der Substrate (Boc-AAD-S-Bzl oder Ac-IEPD-pNA) in DMSO (~ 5 mg / ml) und lagern bei -20 &amp; #176; C. Bereiten Sie eine Arbeitsverdünnung frisch und entsorgen Sie nach jedem Tag, als Boc-AAD-S-Bzl teilweise bei der Lagerung in DMSO hydrolysiert. </li><li> Bereiten Sie eine 250 mM Stamm der farbmetrischen Reagenz (5,5&#39;-Dithio-bis (2-nitrobenzoesäure), DTNB) in DMSO (0,09 g / ml) und bei -20 ° C. Bereiten Sie jeden Tag eine neue Arbeitsverdünnung. Dieses Reagenz ist nur für Substrate mit SBzl Indikatorgruppen nicht pNA erforderlich. </li><li> Make-up frischen Puffer (0,1 M HEPES, 0,05 M MgCl 2, pH 7,3), alle 2-3 Wochen. </li></ol></li><li> Bringen DTNB und synthetische Substrate auf Raumtemperatur. Verdünnen Substrate (01.16, zB 100 ul in 1,6 ml Puffer) und DTNB (1: 250, beispielsweise 10 &amp; mgr; l in 2,5 ml Puffer) und gut mischen. </li><li> Verdünne ein Minimum von 100 &amp; mgr; g Protein-Lysat von jeder Probe in einem Puffer, um ein Endvolumen von 160 ul. Mit einer Mehrkanal-Pipette werden 50 ul pro Vertiefung in dreifacher Ausfertigung (~ 33,3 ug / Vertiefung) in einer &#39;&#39; U &#39;&#39; bottom Vinyl Platte mit 96 Vertiefungen.Fügen Sie eine &quot;Puffer-only&quot; Kontrolle (auch in dreifacher Ausfertigung). </li><li> 100 l verdünnt DTNB zu der Proben / Pufferkontrolle (bei der Arbeit mit Ac-IEPD-pNA lassen Sie diesen Schritt. HINWEIS: Die Spaltung von Ac-IEPD-pNA durch GzmB direkt frei fluorogenen pNA (4B). </li><li> Verwenden Sie eine Mehrkanalpipette um 50 ul verdünnt Substrate auf jeden Satz von dreifach schnell hinzufügen, beginnend mit dem Puffer dann negative Kontrollen und endend mit erwarteten positiven Proben. </li><li> Die Platte wird in der Plattenlesegerät. Messen Asp-ase-Aktivität durch Hydrolyse von Boc-Ala-Ala-Asp-S-Bzl / Ac-IEPD-pNA in einem Mikroplatten-Lesegerät bei OD 405 nm. Verwenden Sie eine kinetische Assay-Protokoll, nehmen 25 Lesungen, alle 15 Sekunden (ca. 6 min Gesamtlesezeit). </li><li> Verwenden Sie die Absorptionswerte zu jedem Zeitpunkt erzeugt werden, um manuell berechnen die Geschwindigkeit der Spaltung des Substrats, wenn die Software des Plattenlesegerät kann kein Wert für Vmax zu generieren. </li></ol> 3. Analyse Data Hinweis: die erzeugt wird, wenn die maximale Geschwindigkeit präsentierten Daten, definiert als Veränderung der OD über die Zeit (mOD / min). <ol><li> Um die Daten zu analysieren, zu bestimmen, die maximale Geschwindigkeit der Spaltung des Substrats, die von der Änderungsrate der Extinktion berechnet wird. Tun Sie dies automatisch mit dem Plattenlesegerät-Software, die in der Regel hat diese Option. </li><li> Alternativ nach der Anzeige der kinetischen Grundabsorptionsänderung, die während der kinetischen Assay auf dem Plattenlesegerät erzeugt werden, manuell auswählen, die Datenpunkte, die den steilsten gerade Linie zu geben. Für die meisten Tests wird innerhalb der ersten 2 min des Tests die maximale Rate erreicht. </li><li> Subtrahieren Sie die Anfangs-OD Lesung aus dem höchsten OD-Wert auf dieser geraden Linie und Gefälle durch das Zeitintervall. Übertragen Sie Rohdaten an Microsoft Excel / Graph-Pad für die statistische Analyse und grafische Darstellung. </li></ol>

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The authors have nothing to disclose.

Historisch die Granzyme wurden als Schlüssel Effektormoleküle zytotoxischer Lymphozyten (CTL und NK-Zellen), die zur Induktion einer schnellen apoptotischen Tod in Zielzellen identifiziert. Dies war vor allem auf die Wirkung von GzmB, das Zielsubstrat Moleküle an Aspartat (D) Reste gespalten und somit konnte die Caspase-Kaskade von beiden spalten pro-Caspasen zu aktivieren, sowie mehrere ihrer nachgelagerten Ziele. Es ist jedoch nun ersichtlich, dass GzmB Expression ist nicht auf lymphoide zytotoxischen Zellen beschr...

Granzyme sind eine Familie von Serin-Proteasen, die in den sekretorischen Lysosomen von natürlichen Killerzellen (NK) und zytotoxischen T-Lymphozyten (CTL) 1 gefunden. Fünf verschiedene Granzyme im Menschen vorhanden (A, B, H, K und M), und zehn Mäuse (A - G, K, M und N) 2,3. Granzyme A und Granzyme B (GZMA, GzmB) sind die häufigsten und wurden umfangreich im menschlichen und Nagetier-Einstellung untersucht. Die klassische Funktion GzmB ist die Induktion von Apoptose in Zielzellen in Verbindung mit der porenbildende Protein von Perforin, Granzym, die die an die Zielzelle Cytosol 4 Zugriff ermöglicht ausgeführt. Obwohl GzmB Expression unzweideutig in zytotoxischen Lymphozyten haben neuere Studien wurden zu einer Vielzahl anderer GzmB exprimierenden Zelltypen, einschließlich, aber nicht beschränkt Keratinozyten 5, 6 Basophilen, Mastzellen 7, plasmacytoid dendritischen Zellen 8, 9 und B-Zellen, 10.In diesem Zusammenhang wurden nicht-apoptotischen GzmB Funktionen ergeben, die von der Teilnahme an entzündlichen Prozessen, Gewebeumbau und anderen immunregulatorischen Eigenschaften 14.11. Da eine breitere biologische Rolle für GzmB als bisher vermutet vorgeschlagen, Forschern erfordern zuverlässige und spezifische Werkzeuge für die Erkennung. Von Vorteil ist, GzmB die ausdrückliche Verpflichtung, in der Carboxylseite von Asparaginsäurereste, eine Eigenschaft, einzigartig unter den eukaryotischen Serinproteasen 15 zu spalten. Maus, Ratte und Mensch sind GzmB strukturell sehr ähnlich, aber die erweiterten Substratspezifität der Maus GzmB unterscheidet dezent von der Ratte und Mensch 16, was bedeutet, dass bestimmte allgemeine Substraten mit Asp an der Klemme (P1) effizient durch GzmB gespalten von allen drei Spezies, während andere Substrate mit komplizierteren Sequenzen stromaufwärts von P1 kann stark unterschiedliche Ergebnisse ergeben. In der Vergangenheit und neuere literature hat diese Tatsache erhebliche Verwirrung und Fehlinterpretation der biologische Bedeutung einiger experimenteller Befunde verursacht, obwohl sorgfältig kontrolliert wurden kinetische Untersuchungen versucht, die Lage 17 zu korrigieren. In dieser Arbeit haben wir versucht, diese Punkte unter Verwendung von zwei im Handel erhältliche Substrate, nämlich Boc-Ala-Ala-Asp-SBzl und N-acetyl-Ile-Glu-Pro-Asp-p-Nitroanilid zu illustrieren. Die beiden Reagenzien zu tun erzeugen unterschiedliche reaktive Gruppen nach der Spaltung (eine freie Sulfhydryl gegenüber einer Leuchtstoff kostenlos Paranitroanilid), aber dies berührt in keiner Weise auf die proteolytische Spaltung. Das beschriebene Protokoll ist eine moderne Adaption eines sehr alten Protokoll 18, sollte aber helfen Forschern, die verschiedenen GzmB Substrate angemessen zu nutzen, sondern schafft auch einen methodischen Rahmen zur Erfassung der Aktivität von anderen Granzyme wie GZMA und GzmH.

<table border="0" cellpadding="0" cellspacing="0" width="1133">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:284px;">Product</td>
			<td style="width:241px;">Company</td>
			<td style="width:181px;">Catalogue number</td>
			<td style="width:427px;">Comment/description</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Boc-Ala-Ala-Asp-S-Bzl</td>
			<td>SM Biochemicals LLC, CA</td>
			<td>SMSB05</td>
			<td>Granzyme B substrate (mouse and human)</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Ac-IEPD-pNA&#160;</td>
			<td>SM Biochemicals LLC, CA</td>
			<td>SMPNA009</td>
			<td>Granzyme B substrate (only human)</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">N-a-CBZ-L-lysine-S-Bzl</td>
			<td>Sigma-Aldrich</td>
			<td>C3647</td>
			<td>Granzyme A substrate</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Suc-Phe-Leu-Phe-S-Bzl</td>
			<td>SM Biochemicals LLC, CA</td>
			<td>SB025</td>
			<td>Granzyme H substrate</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">5,5&#8217;-dithio-bis(2-nitrobenzoic acid)&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>D8130</td>
			<td>&#160;DTNB, Ellman&#8217;s Reagent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">NK cell isolation kit II mouse</td>
			<td>Miltenyi Biotec GmbH</td>
			<td style="width:181px;">130-096-892</td>
			<td style="width:427px;">negative selection kit</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">NK cell isolation kit human</td>
			<td>Miltenyi Biotec GmbH</td>
			<td>130-092-657</td>
			<td style="width:427px;">negative selection kit</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;"></td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Plate reader</td>
			<td>Biorad iMark</td>
			<td></td>
			<td>Biorad Microplate Manager Software Version MPM6.3</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Serocluster U-bottom vinyl 96-well plate</td>
			<td>Corning, MA, USA</td>
			<td>2797</td>
			<td></td>
		</tr>
	</tbody>
</table>

a colorimetric assay that specifically measures granzyme b proteolytic activity: hydrolysis of boc-ala-ala-asp-s-bzl

The serine protease Granzyme B (GzmB) mediates target cell apoptosis when released by cytotoxic T lymphocytes (CTL) or natural killer (NK) cells. GzmB is the most studied granzyme in humans and mice and therefore, researchers need specific and reliable tools to study its function and role in pathophysiology. This especially necessitates assays that do not recognize proteases such as caspases or other granzymes that are structurally or functionally related. Here, we apply GzmB&#8217;s preference for cleavage after aspartic acid residues in a colorimetric assay using the peptide thioester Boc-Ala-Ala-Asp-S-Bzl. GzmB is the only mammalian serine protease capable of cleaving this substrate. The substrate is cleaved with similar efficiency by human, mouse and rat GzmB, a property not shared by other commercially available peptide substrates, even some that are advertised as being suitable for this purpose. This protocol is demonstrated using unfractionated lysates from activated NK cells or CTL and is also suitable for recombinant proteases generated in a variety of prokaryotic and eukaryotic systems, provided the correct controls are used. This assay is a highly specific method to ascertain the potential pro-apoptotic activity of cytotoxic molecules in mammalian lymphocytes, and of their recombinant counterparts expressed by a variety of methodologies.

Die Boc-AAD-S-Bzl Substrat spezifisch für GzmB Die Serinprotease GzmB ist ein Hauptbestandteil von zytotoxischen Lymphozyten (CTL und NK-Zellen) und vorwiegend zur Induzierung schnelle apoptotischen Tod in Zielzellen, wie virusinfizierte oder transformierten Zellen verantwortlich. Dies ist vor allem aufgrund der Substratpräferenz für die Spaltung nach bestimmten Aspartatreste in ausgewählten Proteinen geteilt ein Attribut mit den Caspasen, die auch nach der Aspartatreste...

Watch this Scientific Journal Video about A Colorimetric Assay that Specifically Measures Granzyme B Proteolytic Activity: Hydrolysis of Boc-Ala-Ala-Asp-S-Bzl at JoVE.com

A Colorimetric Assay that Specifically Measures Granzyme B Proteolytic Activity: Hydrolysis of Boc-Ala-Ala-Asp-S-Bzl

We describe a simple, quantitative colorimetric assay that specifically measures the proteolytic activity of human, mouse or rat Granzyme B (GzmB). This protocol can be easily adapted for determining protease activity of other granule serine proteases by the hydrolysis of other synthetic peptide substrates with an appropriate recognition sequence.

Ein Farbtest, die speziell Maßnahmen Granzyme B Proteolytische Aktivität: Hydrolyse von Boc-Ala-Ala-Asp-S-Bzl

The serine protease Granzyme B (GzmB) mediates target cell apoptosis when released by cytotoxic T lymphocytes (CTL) or natural killer (NK) cells. GzmB is ...

a-colorimetric-assay-that-specifically-measures-granzyme-b

Research

JoVE Journal

Chemistry

12.9K Aufrufe.  Peter MacCallum Cancer Centre. We describe a simple, quantitative colorimetric assay that specifically measures the proteolytic activity of human, mouse or rat Granzyme B (GzmB). This protocol can be easily adapted for determining protease activity of other granule serine proteases by the hydrolysis of other synthetic peptide substrates with an appropriate recognition sequence.

Serie: A Colorimetric Assay that Specifically Measures Granzyme B Proteolytic Activity: Hydrolysis of Boc-Ala-Ala-Asp-S-Bzl

Rapid Colorimetric Assays to Qualitatively Distinguish RNA and DNA in Biomolecular Samples

Biochemical experimentation generally requires accurate knowledge, at an early stage, of the nucleic acid, protein, and other biomolecular components in potentially heterogeneous specimens. Nucleic acids can be detected via several established approaches, including analytical methods that are spectrophotometric (e.g., A260), fluorometric (e.g., binding of fluorescent dyes), or colorimetric (nucleoside-specific chromogenic chemical reactions).1 Though it cannot readily distinguish RNA from DNA, the A260/A280 ratio is commonly employed, as it offers a simple and rapid2 assessment of the relative content of nucleic acid, which absorbs predominantly near 260 nm and protein, which absorbs primarily near 280 nm. Ratios &lt; 0.8 are taken as indicative of 'pure' protein specimens, while pure nucleic acid (NA) is characterized by ratios &gt; 1.53.
However, there are scenarios in which the protein/NA content cannot be as clearly or reliably inferred from simple uv-vis spectrophotometric measurements. For instance, (i) samples may contain one or more proteins which are relatively devoid of the aromatic amino acids responsible for absorption at &asymp;280 nm (Trp, Tyr, Phe), as is the case with some small RNA-binding proteins, and (ii) samples can exhibit intermediate A260/A280 ratios (~0.8 &lt; ~1.5), where the protein/NA content is far less clear and may even reflect some high-affinity association between the protein and NA components. For such scenarios, we describe herein a suite of colorimetric assays to rapidly distinguish RNA, DNA, and reducing sugars in a potentially mixed sample of biomolecules. The methods rely on the differential sensitivity of pentoses and other carbohydrates to Benedict's, Bial's (orcinol), and Dische's (diphenylamine) reagents; the streamlined protocols can be completed in a matter of minutes, without any additional steps of having to isolate the components. The assays can be performed in parallel to differentiate between RNA and DNA, as well as indicate the presence of free reducing sugars such as glucose, fructose, and ribose (Figure 1).

A suite of colorimetric assays is described for rapidly distinguishing protein, RNA, DNA, and reducing sugars in potentially heterogeneous biomolecular samples.

Schnelle kolorimetrische Assays zur Qualitativ unterscheiden RNA und DNA in Biomolekulare Proben

Biochemical experimentation generally requires accurate knowledge, at an early stage, of the nucleic acid, protein, and other biomolecular components in ...

Forschung

Chemie

Steady-state, Pre-steady-state, and Single-turnover Kinetic Measurement for DNA Glycosylase Activity

Human 8-oxoguanine DNA glycosylase (OGG1) excises the mutagenic oxidative DNA lesion 8-oxo-7,8-dihydroguanine (8-oxoG) from DNA. Kinetic characterization of OGG1 is undertaken to measure the rates of 8-oxoG excision and product release. When the OGG1 concentration is lower than substrate DNA, time courses of product formation are biphasic; a rapid exponential phase (i.e. burst) of product formation is followed by a linear steady-state phase. The initial burst of product formation corresponds to the concentration of enzyme properly engaged on the substrate, and the burst amplitude depends on the concentration of enzyme. The first-order rate constant of the burst corresponds to the intrinsic rate of 8-oxoG excision and the slower steady-state rate measures the rate of product release (product DNA dissociation rate constant, koff). Here, we describe steady-state, pre-steady-state, and single-turnover approaches to isolate and measure specific steps during OGG1 catalytic cycling. A fluorescent labeled lesion-containing oligonucleotide and purified OGG1 are used to facilitate precise kinetic measurements. Since low enzyme concentrations are used to make steady-state measurements, manual mixing of reagents and quenching of the reaction can be performed to ascertain the steady-state rate (koff). Additionally, extrapolation of the steady-state rate to a point on the ordinate at zero time indicates that a burst of product formation occurred during the first turnover (i.e. y-intercept is positive). The first-order rate constant of the exponential burst phase can be measured using a rapid mixing and quenching technique that examines the amount of product formed at short time intervals (&lt;1 sec) before the steady-state phase and corresponds to the rate of 8-oxoG excision (i.e. chemistry). The chemical step can also be measured using a single-turnover approach where catalytic cycling is prevented by saturating substrate DNA with enzyme (E&gt;S). These approaches can measure elementary rate constants that influence the efficiency of removal of a DNA lesion.

Time courses for the glycosylase activity of 8-oxoguanine DNA glycosylase are biphasic exhibiting a burst of product formation and a linear steady-state phase. Utilizing quench-flow techniques, the burst and the steady-state rates can be measured, which correspond to excision of 8-oxoguanine and release of the glycosylase from the product DNA, respectively.

Steady-State-, Pre-Steady-State-und Einzel-Umsatz Kinetic Measurement für DNA Glycosylase Aktivität

Human 8-oxoguanine DNA glycosylase (OGG1) excises the mutagenic oxidative DNA lesion 8-oxo-7,8-dihydroguanine (8-oxoG) from DNA. Kinetic characterization ...

Fluorescence-based Monitoring of PAD4 Activity via a Pro-fluorescence Substrate Analog

Post-translational modifications may lead to altered protein functional states by increasing the covalent variations on the side chains of many protein substrates. The histone tails represent one of the most heavily modified stretches within all human proteins. Peptidyl-arginine deiminase 4 (PAD4) has been shown to convert arginine residues into the non-genetically encoded citrulline residue. Few assays described to date have been operationally facile with satisfactory sensitivity. Thus, the lack of adequate assays has likely contributed to the absence of potent non-covalent PAD4 inhibitors. Herein a novel fluorescence-based assay that allows for the monitoring of PAD4 activity is described. A pro-fluorescent substrate analog was designed to link PAD4 enzymatic activity to fluorescence liberation upon the addition of the protease trypsin. It was shown that the assay is compatible with high-throughput screening conditions and has a strong signal-to-noise ratio. Furthermore, the assay can also be performed with crude cell lysates containing over-expressed PAD4.

PAD4 is an enzyme responsible for the conversion of peptidyl-arginine to peptidyl-citrulline. Dysregulation of PAD4 has been implicated in a number of human diseases. A facile and high-throughput compatible fluorescence based PAD4 assay is described.

Fluoreszenz-basierte Überwachung von PAD4 Aktivität über eine Pro-Fluoreszenz Substratanalogon

Post-translational modifications may lead to altered protein functional states by increasing the covalent variations on the side chains of many protein ...

Dynamic Electrochemical Measurement of Chloride Ions

This protocol describes the dynamic measurement of chloride ions using the transition time of a silver silver chloride (Ag/AgCl) electrode. Silver silver chloride electrode is used extensively for potentiometric measurement of chloride ions concentration in electrolyte. In this measurement, long-term and continuous monitoring is limited due to the inherent drift and the requirement of a stable reference electrode. We utilized the chronopotentiometric approach to minimize drift and avoid the use of a conventional reference electrode. A galvanostatic pulse is applied to an Ag/AgCl electrode which initiates a faradic reaction depleting the Cl&#713; ions near the electrode surface. The transition time, which is the time to completely deplete the ions near the electrode surface, is a function of the ion concentration, given by the Nernst equation. The square root of the transition time is in linear relation to the chloride ion concentration. Drift of the response over two weeks is negligible (59 &#181;M/day) when measuring 1 mM [Cl&#713;]using a current pulse of 10 Am-2. This is a dynamic measurement where the moment of transition time determines the response and thus is independent of the absolute potential. Any metal wire can be used as a pseudo-reference electrode, making this approach feasible for long-term measurement inside concrete structures.

Dynamic measurement of chloride ions is presented. Transition time of an Ag/AgCl electrode, during a chronopotentiometric technique, can give the concentration of chloride ions in electrolyte. This method does not require a stable conventional reference electrode.

Dynamische elektrochemischen Messung von Chlorid-Ionen

This protocol describes the dynamic measurement of chloride ions using the transition time of a silver silver chloride (Ag/AgCl) electrode. Silver silver ...

A Method to Manipulate Surface Tension of a Liquid Metal via Surface Oxidation and Reduction

Controlling interfacial tension is an effective method for manipulating the shape, position, and flow of fluids at sub-millimeter length scales, where interfacial tension is a dominant force. A variety of methods exist for controlling the interfacial tension of aqueous and organic liquids on this scale; however, these techniques have limited utility for liquid metals due to their large interfacial tension.
Liquid metals can form soft, stretchable, and shape-reconfigurable components in electronic and electromagnetic devices. Although it is possible to manipulate these fluids via mechanical methods (e.g., pumping), electrical methods are easier to miniaturize, control, and implement. However, most electrical techniques have their own constraints: electrowetting-on-dielectric requires large (kV) potentials for modest actuation, electrocapillarity can affect relatively small changes in the interfacial tension, and continuous electrowetting is limited to plugs of the liquid metal in capillaries.
Here, we present a method for actuating gallium and gallium-based liquid metal alloys via an electrochemical surface reaction. Controlling the electrochemical potential on the surface of the liquid metal in electrolyte rapidly and reversibly changes the interfacial tension by over two orders of magnitude ( &#820;500 mN/m to near zero). Furthermore, this method requires only a very modest potential (&#60; 1 V) applied relative to a counter electrode. The resulting change in tension is due primarily to the electrochemical deposition of a surface oxide layer, which acts as a surfactant; removal of the oxide increases the interfacial tension, and vice versa. This technique can be applied in a wide variety of electrolytes and is independent of the substrate on which it rests.

We present a method to control the interfacial energy of a liquid metal in an electrolyte via electrochemical deposition (or removal) of a surface oxide layer. This simple method can control the capillary behavior of gallium-based liquid metals by tuning the interfacial energy rapidly, significantly, and reversibly using modest voltages.

Eine Methode, die Oberflächenspannung eines Liquid Metal manipulieren via Oberfläche Oxidation und Reduktion

Controlling interfacial tension is an effective method for manipulating the shape, position, and flow of fluids at sub-millimeter length scales, where ...

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)

We present herein the optimized synthesis of a triphosphenium bromide salt. Apart from being a versatile metathesis reagent, this unusually stable low-valent-phosphorus-containing compound acts as a useful P+ transfer agent. Unlike traditional methods employed to access low-coordinate phosphorus species which usually require pyrophoric phosphorus-containing precursors (white phosphorus, Tris(trimethylsilyl)phosphine, etc.), or harsh reducing agents (alkali metals, potassium graphite, etc.), the current approach does not involve pyrophoric or explosive reagents and can be done on large scales (&#62;20 g) in excellent yields by undergraduates with basic air-free synthetic training. The bromide counter ion is readily exchanged with other anions such as tetraphenyl borate (described herein) using typical salt metathesis reagents to obtain materials with desired properties and reactivities. The versatility of this P+ transfer approach is exemplified by the reactions of these triphosphenium precursors with an N-heterocyclic carbene and an anionic bisphosphine, each of which readily displace the neutral bisphosphine to give an NHC-stabilized phosphorus(I) cation and a phosphorus(I) containing zwitterion, respectively.

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI

The synthesis of a triphosphenium bromide salt is described and its use as a P+ transfer agent is outlined by reactions with an N-heterocyclic carbene and an anionic bisphosphine, yielding an NHC-stabilized P(I) cation and a P(I) containing zwitterion, respectively.

Vorbereitung und Reaktivität eines Triphosphenium Bromidsalz: eine zweckmäßige und stabile Quelle von Phosphor (I)

We present herein the optimized synthesis of a triphosphenium bromide salt. Apart from being a versatile metathesis reagent, this unusually stable ...

Simultaneous Measurement of HDAC1 and HDAC6 Activity in HeLa Cells Using UHPLC-MS

The search for new histone deacetylase (HDAC) inhibitors is of increasing interest in drug discovery. Isoform selectivity has been in the spotlight since the approval of romidepsin, a class I HDAC inhibitor for cancer therapy, and the clinical investigation of HDAC6-specific inhibitors for multiple myeloma. The present method is used to determine the inhibitory activity of test compounds on HDAC1 and HDAC6 in cells. The isoform activity is measured using the ultra-high-performance liquid chromatography &#8211; mass spectrometry (UHPLC-MS) analysis of specific substrates incubated with treated and untreated HeLa cells. The method has the advantage of reflecting the endogenous HDAC activity within the cell environment, in contrast to cell-free biochemical assays conducted on isolated isoforms. Moreover, because it is based on the quantification of synthetic substrates, the method does not require the antibody recognition of endogenous acetylated proteins. It is easily adaptable to several cell lines and an automated process. The method has already proved useful in finding HDAC6-selective compounds in neuroblasts. Representative results are shown here with the standard HDAC inhibitors trichostatin A (non-specific), MS275 (HDAC1-specific), and tubastatin A (HDAC6-specific) using HeLa cells.

The present method serves to identify isoform-specific inhibitors of histone deacetylases (HDAC) in HeLa cells by the UHPLC-MS analysis of multiple substrates. This is an antibody-free method developed to reflect HDAC1 and HDAC6 activity in the living cell environment, in contrast to single-isoform cell-free assays.

Gleichzeitige Messung von HDAC1 und HDAC6 Tätigkeit in HeLa-Zellen mit UHPLC-MS

The search for new histone deacetylase (HDAC) inhibitors is of increasing interest in drug discovery. Isoform selectivity has been in the spotlight since ...

Microfluidic Preparation of Liquid Crystalline Elastomer Actuators

This paper focuses on the microfluidic process (and its parameters) to prepare actuating particles from liquid crystalline elastomers. The preparation usually consists in the formation of droplets containing low molar mass liquid crystals at elevated temperatures. Subsequently, these particle precursors are oriented in the flow field of the capillary and solidified by a crosslinking polymerization, which produces the final actuating particles. The optimization of the process is necessary to obtain the actuating particles and the proper variation of the process parameters (temperature and flow rate) and allows variations of size and shape (from oblate to strongly prolate morphologies) as well as the magnitude of actuation. In addition, it is possible to vary the type of actuation from elongation to contraction depending on the director profile induced to the droplets during the flow in the capillary, which again depends on the microfluidic process and its parameters. Furthermore, particles of more complex shapes, like core-shell structures or Janus particles, can be prepared by adjusting the setup. By the variation of the chemical structure and the mode of crosslinking (solidification) of the liquid crystalline elastomer, it is also possible to prepare actuating particles triggered by heat or UV-vis irradiation.

This article describes the microfluidic process and parameters to prepare actuating particles from liquid crystalline elastomers. This process allows the preparation of actuating particles and the variation of their size and shape (from oblate to strongly prolate, core-shell, and Janus morphologies) as well as the magnitude of actuation.

Mikrofluidische Vorbereitung der flüssigen kristallenen Elastomer Aktoren

This paper focuses on the microfluidic process (and its parameters) to prepare actuating particles from liquid crystalline elastomers. The preparation ...

A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species

&#945;-Functionalization of ketones via umpolung of enolates by hypervalent iodine reagents is an important concept in synthetic organic chemistry. Recently, we have developed a two-step strategy for ketone enolate umpolung that has enabled the development of methods for chlorination, azidation, and amination using azoles. In addition, we have developed C-C bond&#8211;forming arylation and allylation reactions. At the heart of these methods is the preparation of the intermediate and highly reactive enolonium species prior to addition of a reactive nucleophile. This strategy is thus reminiscent of the preparation and use of metal enolates in classical synthetic chemistry. This strategy allows the use of nucleophiles that would otherwise be incompatible with the strongly oxidizing hypervalent iodine reagents. In this paper we present a detailed protocol for chlorination, azidation, N-heteroarylation, arylation, and allylation. The products include motifs prevalent in medicinally active products. This article will greatly assist others in using these methods.

A two step one-pot protocol for the umpolung of ketone enolates to enolonium species and addition of a nucleophile to the &#945;-position is described. Nucleophiles include chloride, azide, azoles, allyl-silanes, and aromatic compounds.

Ein zweistufiges Protokoll für die Umpolung Funktionalisierung von Ketonen über Enolonium Arten

&#945;-Functionalization of ketones via umpolung of enolates by hypervalent iodine reagents is an important concept in synthetic organic chemistry. ...

Synthesis of Esters Via a Greener Steglich Esterification in Acetonitrile

The Steglich esterification is a widely-used reaction for the synthesis of esters from carboxylic acids and alcohols. While efficient and mild, the reaction is commonly performed using chlorinated or amide solvent systems, which are hazardous to human health and the environment. Our methodology utilizes acetonitrile as a greener and less hazardous solvent system. This protocol exhibits rates and yields that are comparable to traditional solvent systems and employs an extraction and wash sequence that eliminates the need for the purification of the ester product via column chromatography. This general method can be used to couple a variety of carboxylic acids with 1&#176; and 2&#176; aliphatic alcohols, benzylic and allylic alcohols, and phenols to obtain pure esters in high yields. The goal of the protocol detailed here is to provide a greener alternative to a common esterification reaction, which could serve useful for ester synthesis in both academic and industrial applications.

A modified Steglich esterification reaction was used to synthesize a small library of ester derivatives with primary and secondary alcohols. The methodology uses a non-halogenated and greener solvent, acetonitrile, and enables product isolation in high yields without the need for chromatographic purification.

Synthese von Estern über ein grüner Steglich-Veresterung in Acetonitril

The Steglich esterification is a widely-used reaction for the synthesis of esters from carboxylic acids and alcohols. While efficient and mild, the ...