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EnzyChromTM Creatine Kinase Assay Kit (ECPK-100)

Colorimetric Determination of Creatine Kinase Activity at 340 nm

DESCRIPTION

CREATINE KINASE (CK), also known as creatine phosphokinase (CPK), is an enzyme (EC 2.7.3.2) expressed predominantly in skeletal muscle, smooth muscle and the brain. The CK enzyme consists of two subunits, which can be either B (brain type) or M (muscle type), and hence three different isoenzymes: CK-MM, CK-BB and CK-MB. CK catalyzes the conversion of creatine to phosphocreatine, consuming adenosine triphosphate (ATP) and generating adenosine diphosphate (ADP) and the reverse reaction. CK is often determined routinely in emergency patients with chest pain and acute renal failure. Elevation of CK is an indication of damage to muscle and has been associated with injury, rhabdomyolysis, myocardial infarction, myositis, myocarditis, malignant hyperthermia and neuroleptic malignant syndrome, etc. Lower levels can be an indication of alcoholic liver disease and rheumatoid arthritis. Simple, direct and automation-ready procedures for measuring CK activity are very desirable. BioAssay Systems' QuantiChromTM Creatine Kinase Assay Kit is based on enzyme coupled reactions in which creatine phosphate and ADP is converted to creatine and ATP by CK, the generated ATP is used to phosphorylate glucose by hexokinase to generate glucose-6-phosphate, which is then oxidized by NADP in the presence of glucose-6- phosphate dehydrogenase.

The produced NADPH, measured at 340 nm, is proportionate to the CK activity in the sample.

APPLICATIONS

Direct Assays: CK in serum, plasma and other biological samples.

Pharmacology: effects of drugs on CK activity.

KEY FEATURES

Sensitive and accurate. Detection range: 5 to 300 U/L creatine kinase in 96-well plate assay.

Convenient. The procedure involves adding a single working reagent, and reading the optical density at 10 min and 40 min at room temperature or 37°C.

High-throughput. Can be readily automated as a high-throughput 96- well plate assay for thousands of samples per day.

KIT CONTENTS (100 tests in 96-well plates)

Assay Buffer: 12 mL Substrate Solution: 1.0 mL

Enzyme Mix: 120 μL Calibrator: 150 μL

Storage conditions. This kit is shipped on dry ice. Store all reagents at -20°C. Shelf life of at least 6 months (see expiry dates on labels).

Precautions: reagents are for research use only. Normal precautions for laboratory reagents should be exercised while using the reagents. Please refer to Material Safety Data Sheet for detailed information.

PROCEDURES

Sample Preparation. Use non-hemolyzed samples. Samples should be assayed within 4 hours of blood collection if they remain at room temperature, or within 12 hours if stored at 4°C. Samples can be stored at -80°C and should be thawed only once. If turbidity is observed, centrifuge sample and use clear supernatant for assay.

Reagent Reconstitution. Bring all components to room temperature.

For each reaction well, mix 10 μL Substrate Solution, 100 μL Assay Buffer and 1 μL Enzyme Mix. Fresh reconstitution is recommended. If the assay is to be carried out at 37°C, warm up the Reconstituted Reagent at 37°C.

1. Calibrator: transfer 110 μL water and (10 μL Calibrator + 100 μL water) into separate wells of a clear bottom 96-well plate.

Samples: transfer 10 μL samples into separate wells. Add 100 μL Reconstituted Reagent and tap plate to mix.

2. Reaction. Incubate at room temperature or 37°C. CK is fully activated within 10 min by glutathione provided in the Substrate

Solution. Read OD340nm at 10 min and again at 40 min.

3. Calculation. Calculate sample CK activity using the equation,

OD40min and OD10min are OD340nm values at 40 min and 10 min for the sample. ODCALIBRATOR and ODH2O are OD340nm values of the Calibrator and water blank at 40 min. The value 100 is the equivalent activity (U/L) of the Calibrator under the assay conditions. Unit definition: one unit of CK will transfer 1 μmole of phosphate from phosphocreatine to ADP per min at pH 6.0.

Note: If the CK activity is expected to be higher than 300 U/L, read OD340nm at 10 min and again at 15 min. To calculate the CK activity replace (OD40min – OD10min) with (OD15min – OD10min) and replace the factor 100 with 600 in the above equation. Linear range: 30 to 1,800 U/L CK activity.

MATERIALS REQUIRED, BUT NOT PROVIDED

Pipeting (multi-channel) devices. Clear-bottom 96-well plates (e.g. Corning Costar) and plate reader.

GENERAL CONSIDERATIONS

This assay is based on an enzyme-catalyzed kinetic reaction. Addition of Reconstituted Reagent should be quick and mixing should be brief but thorough. Use of multi-channel pipettor is recommended.

EXAMPLES

Samples were assayed in duplicate using the 96-well protocol. The CK activity (U/L) was 12.0 ± 0.9 for a rat serum sample, 11.0 ± 0.5 for human serum, 28 ± 1 for human plasma, 9.0 ± 0.8 for mouse serum and 49 ± 2 for bovine serum.

PUBLICATIONS

1. Itaka K et al (2010). Polyplex nanomicelle promotes hydrodynamic gene introduction to skeletal muscle. J Control Release. 143(1):112-9.

2. Steen C et al (2010). Reduced Creatine Kinase B Activity in Multiple Sclerosis Normal Appearing White Matter. PLoS One 5(5):e10811.

3. Kwon S et al. (2010). ASB9 interacts with ubiquitous mitochondrial creatine kinase and inhibits mitochondrial function. BMC Biol. 8:23.

 

EnzyChromTM Kinase Assay Kit (EKIN-400)

Fluorimetric high-throughput kinase assay

DESCRIPTION

KINASES, also known as phosphotransferases, constitute a large family of enzymes that transfer phosphate groups from the high-energy donor molecule ATP, to their specific substrates. Kinases are known to regulate the majority of cellular processes. The largest group of this family is the protein kinases. So far, 518 different kinases have been identified in humans and up to 30% of human proteins are modified by these kinases. The enormous diversity and their key role in cellular signaling make them ideal targets for drug developments. BioAssay Systems’ EnzyChromTM Kinase Assay Kit provides a simple and rapid method for assaying kinase activity and high-throughput screening for kinase inhibitors. This homogeneous microplate-based assay involves incubating the kinase with a single working reagent, in which ADP is enzymatically converted to ATP and pyruvate, which is quantified using a fluorimetric (530nm/590nm) assay method.

KEY FEATURES

Safe. Non-radioactive assay.

Sensitive and accurate. As low as 0.01 U/L kinase can be quantified.

Homogeneous and convenient. "Mix-incubate-measure" type assay. The whole assay involves adding a single working reagent and incubation for 10 min at room temperature.

Robust and amenable to HTS: Assay can tolerate up to 300 μM ATP and 10% dimethylsulfoxide (DMSO). Z’ factors of > 0.6 are routinely observed in 96/384-well plates. Can be readily automated on HTS liquid handling systems for tens of thousands of assays per day.

APPLICATIONS

Kinase activity assays and HTS for kinase inhibitors.

ADP determination in cells and other biological samples.

KIT CONTENTS

Reagent A: 10 mL R eagent B: 10 mL

Assay Buffer: 25 mL S t andard: 100 μL 3 mM ADP

Storage conditions: store all reagents at -20°C. This product is shipped on dry ice. Shelf life of at least 6 months.

Precautions: reagents are for research use only. Normal precautions for laboratory reagents should be exercised while using the reagents. Please refer to Material Safety Data Sheet for detailed information.

ASSAY PROCEDURE

This kit is sufficient for 400 assays in 384-well plate (200 assays in 96-well plate). Use black flat-bottom plates. Prior to assay, bring all reagents to room temperature. Assays in duplicate wells are recommended. Interference: thiols (b-mercaptoethanol, dithioerythritol etc) at > 10 μM interfere with this assay and should be avoided.

Kinase Activity Assay in 384-well Plate

1. Kinase Reaction. Users should provide their own enzyme, ultra-pure ATP (e.g. Sigma # A7699) and substrate. Set up 20 μL reaction mixture containing the kinase, ATP and substrate in the provided Assay Buffer (pH 7.0) or any suitable kinase buffer. Set up a Blank Control that contains ATP and substrate but no enzyme. Incubate at desired temperature for desired period of time e.g. 30 min.

2. Standards. Prepare 900 μL 10 μM ADP Premix by mixing 3 μL 3 mM Standard and 897 μL distilled water. Dilute standard as follows. Transfer 20 μL standards into separate wells of the plate.

3. ADP Detection. Prepare enough Working Reagent for each well by mixing 25 μL Reagent A and 25 μL Reagent B. Add 40 μL Working Reagent to each assay well. Tap plate to mix. Incubate at room temperature for 10 min.

4. Read fluorescence intensity at lexc = 530nm and lem = 590nm. Calculate kinase activity,

where DFSAMPLE = (fluorescence intensity of sample well – fluorescence of the blank well), slope is the slope of the ADP standard curve. t is the kinase reaction time (e.g. 30 min). Vol is the volume (μL) of kinase added to the 20 μL reaction.

Note: typical kinase assays use 100 to 200 μM ATP. If DFSAMPLE > (F10μM ADP – FH2O), dilute enzyme in assay buffer. Repeat the assay, multiply the results by the dilution factor n. This will ensure that the initial rate is measured at < 10% ATP conversion.

High-throughput Screen for Kinase Inhibitors

For inhibitor screens, test compounds are usually pre-incubated with kinase for 10 to 30 min, prior to adding ATP/substrate to initiate kinase reaction. After a 30-min kinase reaction, the produced ADP is quantified using the fluorimetric assay. The fluorescence intensity will be decreased in the presence of an inhibitor.

1. Controls and compounds. Use a known kinase inhibitor (e.g. staurosporine) as a positive control. Alternatively, “no enzyme” wells can serve as a positive control. Use the same volume of the compound solvent (e.g. DMSO) as an inhibitor negative control.

Example: transfer 5 μL test compound, control inhibitor and negative control (e.g. DMSO) to appropriate wells, add 10 μL enzyme solution to all assay wells. Apply an “in-well” mixing step. Incubate for 10 to 30 min.

2. Kinase Reaction. Add 5 μL mixture containing ATP and the kinase substrate to each assay well. Mix well. Incubate for desired period of time (e.g. 30 min).

3. ADP Detection. Prepare enough Working Reagent by mixing 25 μL Reagent A and 25 μL Reagent B. Add 40 μL Working Reagent to each well and mix well. Incubate for 10 min.

4. Read fluorescence intensity at lexc = 530nm and lem = 590nm.

LITERATURE

[1]. Manning G. et al. (2002). The protein kinase complement of the human genome. Science 298: 1912-1934.

[2]. Grant SK. (2009). Therapeutic protein kinase inhibitors. Cell Mol Life Sci. 66(7):1163-1177.