A
TBS-380 Mini-Fluorometer Method for DNA Quantitation Using
PicoGreen®
1. INTRODUCTION
PicoGreen®
dsDNA Quantitation Reagent is an ultra-sensitive fluorescent nucleic acid stain
for quantitating double-stranded DNA (dsDNA) in molecular biology procedures.
These procedures include cDNA synthesis for library production, DNA fragment
purification for subcloning, and diagnostic applications, such as quantitating
DNA amplification products1,2 and primer extension assays.3,4
The conventional technique for measuring nucleic acid concentrations is the
determination of absorbance at 260 nm (A260). The major disadvantages
of the absorbance method are the relative large contribution of nucleotides,
single-stranded nucleic acids and proteins to the signal, the interference
caused by con-tami-nants commonly found in nucleic acid preparations, the
inability to distinguish between DNA and RNA, and the relative insensitivity of
the assay (an A260 of 0.1 corresponds to a 5 µg/mL dsDNA solution).
Hoechst (bisbenzimide) dyes are sensitive fluorescent nucleic acid stains that
circumvent many of these problems. The Hoechst 33258 - based assay is somewhat
selective for dsDNA, does not show significant fluorescence enhancement in the
presence of proteins and allows the detection and quantitation of DNA
concentrations as low as 10 ng/mL DNA.5
The Turner BioSystems TBS-380 Mini-Fluorometer used in conjunction with
Molecular Probes' PicoGreen® dsDNA Quantitation Reagent enables
researchers to quantitate as little as 500 pg/mL of dsDNA in 2 mL assay volume.
When the Minicell adaptor is used, researchers can quantitate 50 pg dsDNA in a 2
µL assay volume. This sensitivity exceeds that achieved with the Hoechst 33258
- based assay by 20-fold.
The linear detection range of the PicoGreen® assay in the TBS-380
Mini-Fluorometer extends over three orders of magnitude in DNA concentration -
from 500 pg/mL to 500 ng/mL - with a single dye concentration (see figures).
This linearity is maintained in the presence of several compounds commonly found
to contaminate nucleic acid preparations, including salts, urea, ethanol,
chloroform, detergents, proteins and agarose. The assay protocol has been
developed to minimize the fluorescence contribution of RNA and single-stranded
DNA (ssDNA). Using the PicoGreen® dsDNA Quantitation Reagent and the
TBS-380 Mini-Fluorometer, researchers can quantitate dsDNA in the presence of
equimolar concentrations of ssDNA and RNA with minimal effect on the
quantitative results.
2. MATERIALS REQUIRED
· TBS-380 Mini-Fluorometer (P/N 3800-003).
· 10x10 mm square polystyrene disposable cuvettes (P/N 7000-957).
· Minicell Adaptor Kit (P/N 3800-928).
· PicoGreen® dsDNA Quantitation Reagent, supplied by Molecular
Probes, Inc., Eugene, Oregon, catalog number P-7581. A single 1 mL unit of the
reagent concentrate is sufficient for 200 assays using an assay volume of 2 mL
and the protocol described in Section 3. Handling, storage and use of the
reagent should be performed in accordance with the product information sheet
supplied by Molecular Probes, Inc.
3.
EXPERIMENTAL PROTOCOL
3.1 Reagent
Preparation
The PicoGreen® dsDNA Quantitation Reagent is supplied as a 1 mL
concentrated dye solution in anhydrous dimethylsulfoxide (DMSO). On the day of
the experiment, prepare a 2X working solution of the PicoGreen®
Reagent by making a 1:200 dilution of the concentrated dye solution in 1xTE (10
mM Tris-HCl, 1 mM EDTA, pH 7.5). To prepare enough working solution to assay 20
samples, add 100 µL
PicoGreen® dsDNA Quantitation Reagent to 20.0 mL of 1xTE. Preparing
this solution in a plastic container is recommended, as the reagent may adsorb
to glass surfaces. Protect the working solution from light by covering it with
foil or placing it in the dark, as the PicoGreen® Reagent is
susceptible to photodegradation.
For best results, this solution should be used within a few hours of its
preparation.
3.2 DNA
Standard Curve
3.2.1 Prepare a 1 µg/mL stock solution of dsDNA in 1xTE. Determine the
DNA concentration on the basis of absorbance at 260 nm (A260) in a
cuvette with a 1cm pathlength; an A260 of 0.02 corresponds to 1 µg/mL
dsDNA solution. Calf thymus DNA is commonly used for a standard curve, although
any purified dsDNA preparation may be used. It is preferable to prepare the
standard curve with DNA similar to the type being assayed; long or short linear
DNA fragments for quantitating similarsized restriction fragments; plasmid for
quantitating plasmid DNA. However, most linear dsDNA molecules have been found
to yield approximately equivalent signals, regardless of fragment length. The
PicoGreen® assay remains linear in the presence of
several compounds that commonly contaminate nucleic acid preparations, although
the signal intensity may be affected. Thus, to serve as an effective control,
the dsDNA solution used to prepare the standard curve should be treated the same
way as the experimental samples and should contain similar levels of such
compounds.
3.2.2 To generate a single-replicate, eight-point standard curve from 0.5 ng/mL
to 500 ng/mL (as shown in Table 1), prepare a series of DNA solution at 2X final
concentration, mix equal volume of the 2X DNA solution with the 2X PicoGreen®
working solution into 10x10 mm disposable cuvettes. For blank, mix equal volume
of 1X TE with the 2X PicoGreen® working solution. Incubate for 2 to
5 minutes at room temperature, protected from light.
|
2X DNA
solution concentration (ng/mL )
|
Volume
of the 2X DNA solution (mL)
|
Volume
of the 2X PicoGreen®
solution (mL)
|
Final
DNA concentration in PicoGreen® Assay (ng/mL)
|
|
1000
|
1
|
1
|
500
|
|
200
|
1
|
1
|
100
|
|
50
|
1
|
1
|
25
|
|
20
|
1
|
1
|
10
|
|
5
|
1
|
1
|
2.5
|
|
2
|
1
|
1
|
1
|
|
1
|
1
|
1
|
0.5
|
|
0
|
1
|
1
|
blank
|
Table 1. DNA
standard curve for 10x10 mm cuvette.
3.2.3
PicoGreen® Assay can also be performed in lower assay volume when
Minicell Adaptor is used. The assay volume ranges from 50 µL
to 200 µL.
To generate standard curve from 1 ng/mL to 100 ng/mL (as shown in Table 2),
prepare a series of DNA solution at 2X final concentration, mix equal volume of
the 2X DNA solution with the 2X PicoGreen® working solution. Mix
well and transfer at least 50 µL
of the mix to the Minicell cuvette. Be sure not to introduce any air bubbles in
your samples. Slight tapping on the outside cuvette wall will often help
dissipate bubbles. Incubate for 2 to 5 minutes at room temperature, protected
from light.
|
2X DNA
solution concentration (ng/mL)
|
Volume
of the 2X DNA solution (µL)
|
Volume
of the 2X dye
solution (µL)
|
Final
DNA concentration in PicoGreen Assay (ng/mL)
|
|
200
|
30
|
30
|
100
|
|
50
|
30
|
30
|
25
|
|
20
|
30
|
30
|
10
|
|
5
|
30
|
30
|
2.5
|
|
2
|
30
|
30
|
1
|
|
0
|
30
|
30
|
blank
|
Table 2. DNA
standard curve for Minicell cuvette.
3.2.4
After incubation, measure the sample fluorescence in the TBS-380
Mini-Fluorometer. Select the BLUE channel. Calibrate the instrument with the
most fluorescent sample.
3.2.5 Measure the fluorescence of the remaining samples. The TBS-380
Mini-Fluorometer will give a direct concentration read out, and data may be used
to generate a standard curve of reading versus DNA concentration.
Figure 1A . PicoGreen® Standard plot
Figure 1B: Enlargement of lower left segment of Figure 1A
3.3 Sample
Analysis
3.3.1 Dilute the unknown DNA samples in 1X TE to a desired volume (1.0 mL
for 10x10 mm cuvette or 25-100 µL for Minicell). A higher dilution of the
experimental sample will ensure that any contaminants are maximally diluted.
However, extremely small sample volumes should be avoided because they are
difficult to pipet accurately. See Section 3.4 for information on eliminating
RNA and ssDNA from the sample.
3.3.2 Add equal volume of the 2X working solution of the PicoGreen®
Reagent (prepared in section 3.1) to each sample, mix well and transfer the mix
to the proper cuvette. Incubate for 2 to 5 minutes at room temperature,
protected from light.
3.3.3 The assay may be repeated using a different dilution of the sample
to confirm the quantitation results.
3.4 Eliminating Single-Stranded Nucleic Acids from Samples
Double-stranded DNA can be quantitated in the presence of equimolar
concentrations of single-stranded nucleic acids with minimal interference. A
10-fold excess of RNA over dsDNA generally produces no more than a 10% change in
the fluorescence signal. Somewhat larger distortions are produced by ssDNA,
particularly at low DNA concentrations (see Molecular Probes' product
information sheet MP7581 for more details). Fluorescence due to PicoGreen®
Reagent binding to RNA at high concentrations can be eliminated by
treating the sample with DNase-free RNase.6 The use of RNase A/RNase
T1 with S1 nuclease will eliminate all single-stranded nucleic acids and ensure
that the entire sample fluorescence is due to dsDNA.6
4. REFERENCES
1. Nucleic Acids Res. 24, 2623 (1996)
2. BioTechniques 21, 372 (1996)
3. BioTechniques 21, 664 (1996)
4. Proc. Natl. Acad. Sci. USA 93, 6091 (1996)
5. Anal. Biochem. 102, 344 (1980)
6. Molecular Cloning: A Laboratory Manual, Second Edition, J. Sambrook,
E.F. Fritsch and T. Maniatis, Cold Spring Harbor Laboratory Press, Cold Spring
Harbor, New York (1989).
5. PATENTS AND TRADEMARKS
The PicoGreen® dsDNA Quantitation Reagent is the subject of patent
applications filed by Molecular Probes, Inc. and is not available for resale or
other commercial uses without a specific agreement from Molecular Probes, Inc.
PicoGreen is a registered trademark of Molecular Probes, Inc.
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