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CAT Reporter Gene Assays

Overview


The determination of chloroamphenicol acetyltransferase (CAT) enzyme activity is a standard method for assessing promotor expression in transfected cell lines. In such assays the promoter sequence of interest is fused to a DNA sequence encoding the bacterial CAT enzyme, an enzyme which is not expressed in trhe mammalian cell line. The enzyme catalyzes acylation of chloramphenicol, primarly at the 3-hydroxyl position. Quantificaation of the acetyl-chloramphenicol (AcCAM) generated provides a convenient measure of promoter activity.

The rapid two-phase CAT assay described here utilizes acetyl-1-14C Acetyl Coenzyme A or acetyl-3H Acetyl Coenzyme A as the labeled substrate. In this method the enzymatic reaction components are combined directly in a mini scintillation vial and then immediately overlaid with 5 mL of a water-immiscible counting cocktail. The 14C or 3H AcCAM generated by the reaction diffuses linearly over time into the organic phase of the cocktail. Direct liquid scintillation counting (LSC) of the two-phase reaction mix in the vial provides quantitative data reflecting the CAT activity. The rate of the enzymatic reaction, as determined by the rate of increase in cpm/min, is directly propotional to the concentration of CAT in the reaction.

This method does not require any extractions or TLC autoradiography. The assay provides a continuous data stream from a single reaction, as opposed to the data from an an end-point reaction. Other advantages are that the specific activity and radiochemical concentration is constant and preadjusted for direct use in the assay. No additional concentration adjustments are required and lot-to-lot variation is thus eliminated.

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What do I need to run this assay?


Reagents available from PerkinElmer:

  • 14C Acetyl Coenzyme A, CAT Assay Grade (Cat. No. NEC313L) or 3H Acetyl Coenzyme A, CAT Assay Grade (Cat. No. NET290L)
  • Scintillation cocktail
  • Pico Glass Vials, 7 mL (Cat. No. 6000167)

Reagents available from other suppliers:

  • Chloramphenicol (Sigma Aldrich Cat. No. C0378)
  • E.coli chloramphenicol acetyltransferase (Promega Cat. No. E1051)
  • CAT assay buffer (100 mM Tris buffer, pH 7.8)

Instrumentation/Equipment:

  • A Liquid scintillation counting-capable reader (We recommend the Tri-Carb or MicroBeta2™ or TopCount NXT™.)

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Protocol-in-brief


cat_workflow_ASK.jpg
CAT workflow

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Step-by-step protocol


  1. To each 7 mL glass vial, add 50 μL of cell extract or CAT enzyme standard in CAT assay buffer (100 mM Tris buffer, pH 7.8).
  2. To this sample add 200 μL of premix containing 1.25 mM Chloramphenicol in CAT assay buffer. 
  3. Initiate the reaction by adding the radiolabeled substrate containing 0.1 μCi of 14C Acetyl Coenzyme A or 0.5 μCi of 3H Acetyl Coenzyme A in 22.5 μL of 1 mM unlabeled acetyl Coenzyme A. These additions result in a 0.1 mM final concentration of acetyl CoA. 
  4. Gently overlay the reaction with 5 mL of Insta-Fluor Plus scintillation cocktail. 
  5. Close the vials and incubate at room temperature.
  6. At timed intervals, count the vials sequentially in a liquid scintillation counter for 0.10 min. Final experimental resulats are obtained in 1-2 hours, although the assay can be terminated at any point at which counts above background are obtained. 
  7. Plot cpm vs. time for each reaction. 
  8. Determine CAT enzyme activity by comparison to a standard curve, with the data expressed as the increase in cpm/min.

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Citations


  1. Crabb, D. and Dixon, J. A method for increasing the sensitivity of chloramphenicol acetyltransferase assays in extracts of transfected cultured cells Anal. Biochem. 163, 88-92 (1987) Link 
  2. Hsu, J.C. et al. Indole-3-carbinol inhibition of androgen receptor expression and downregulation of androgen responsiveness in human prostate cancer cells. Carcinogenesis 26, 1896 -1904 (2005). Link 
  3. Neumann, J. et al. A novel rapid assay for chloramphenicol acetyltransferase gene expression Biotechniques 5,444-448 (1987) 
  4. Tsumaki, N., Liu, Y., Yamada, Y. & Krebsbach, P. Enhancer analysis of the alpha 1(II) and alpha 2(XI) collagen genes in transfected chondrocytes and transgenic mice. Methods Mol. Biol 139, 187-195 (2000). Link 
  5. Zhang, S., Jonklaas, J. & Danielsen, M. The glucocorticoid agonist activities of mifepristone (RU486) and progesterone are dependent on glucocorticoid receptor levels but not on EC50 values. Steroids 72, 600-608 (2007). Link

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Tips and troubleshooting


Tips

  • To generate a continuous data stream, the scintillation cocktail should be added to the vial immediately after initiation of the CAT reaction. Adding the cocktail at a later time point does not significanly reduce the diffusion time, but will extend the overall assay time.
  • Note that the cell extract samples in step 1 of the protocol may require a 15 min heat treatment at 70 °C to destroy interfering acylases. The need for this step is  cell-line dependent.

FAQs


Q. Do I need to shake or vortex the sample?
A. To maintain linearity and reproducibility of experimental results, mixing of the two phases should be avoided. Shaking or vortexing the sample disperses the aqueous phase and adequate time must be allowed for complete phase separation to occur prior to counting the samples.

Q. Can I incubate at temperatures other than room temperature?
A. Yes, incubation at 37 °C is possible if acceleration of the reaction is desired.

Q. What is the sensitivity of the assay?
A. Experiments utilizing 5 μCi of 3H Acetyl CoA have shown linearity down to CAT levels of 0.0025 units.

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Other reporter gene assays available from PerkinElmer


Luciferase reporter gene assay reagents

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Custom conjugation and custom assay development at PerkinElmer


PerkinElmer offers custom radiochemical services as well as custom assay development. If you are interested in having your biomolecule custom-radiolabeled or in custom assay development, please contact our custom teams:

ON>POINT® Custom Radiolabeling Services

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