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WO1999042620A2 - Articles manufactures et procedes de marquage de biomolecules - Google Patents

Articles manufactures et procedes de marquage de biomolecules Download PDF

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Publication number
WO1999042620A2
WO1999042620A2 PCT/US1999/003704 US9903704W WO9942620A2 WO 1999042620 A2 WO1999042620 A2 WO 1999042620A2 US 9903704 W US9903704 W US 9903704W WO 9942620 A2 WO9942620 A2 WO 9942620A2
Authority
WO
WIPO (PCT)
Prior art keywords
article
backing
biomolecules
indicator
manufacture according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US1999/003704
Other languages
English (en)
Other versions
WO1999042620A3 (fr
WO1999042620A9 (fr
Inventor
Jack G. Chirikjian
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Edvotek
Original Assignee
Edvotek
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Edvotek filed Critical Edvotek
Priority to EP99908309A priority Critical patent/EP1057001A2/fr
Priority to CA002321100A priority patent/CA2321100A1/fr
Priority to AU27771/99A priority patent/AU2777199A/en
Priority to JP2000532558A priority patent/JP2002504351A/ja
Publication of WO1999042620A2 publication Critical patent/WO1999042620A2/fr
Publication of WO1999042620A3 publication Critical patent/WO1999042620A3/fr
Publication of WO1999042620A9 publication Critical patent/WO1999042620A9/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • G01N33/5436—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals with ligand physically entrapped within the solid phase
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6806—Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/30—Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis

Definitions

  • Electrophoresis techniques have become principal tools for characterizing biomolecules.
  • the method is based on the fact that macromolecules such as DNA, RNA and proteins possess a charge and can therefore move in an electric field through sieving materials such as agarose or poly aery la ide.
  • the application of electrophoretic techniques has required the development of chemical indicators for use in visualizing separated macromolecules.
  • One such indicator used to visualize DNA is ethidium bromide (EtBr).
  • EtBr ethidium bromide
  • the disadvantage of this widely used stain is that it is a potent mutagen.
  • the potential personal hazard of directly contacting such a solution and the environmental hazard of pouring it or other hazardous chemicals down the drain has resulted in a need for a better and safer method of preparing, using and disposing of such toxic solutions.
  • an object of the present invention to provide a readily manufacturable apparatus capable of safely staining or labeling biomolecules.
  • an article of manufacture comprising a flexible backing and a dry coating adhered to a surface of the backing, wherein the coating comprises an indicator that stains or labels a biomolecule.
  • the backing promotes good contact with a gel containing a biomolecule, is impermeable, allows the coating solution to be evenly spread and dried and is easily dispensable.
  • the coating solution is selected from the group consisting of starch, glue, gum, flour, agarose or polyacrylamide, or mixtures of two or more of these.
  • the indicator is selected from the group consisting of stains, dyes or labeled probes.
  • a method for staining or labeling biomolecules comprising applying an article of manufacture comprising a flexible backing and a dry coating adhered to a surface of the backing, wherein the coating comprises an indicator that stains or labels a biomolecule, to a gel or support containing the biomolecules for a sufficient period of time to allow diffusion to the biomolecules.
  • kits suitable for use in a method for staining or labeling biomolecules comprising (A) an article of manufacture comprising a flexible backing and a dry coating adhered to a surface of the backing, wherein the coating comprises an indicator that stains or labels a biomolecule; (B) reagents to effect staining or labeling of the biomolecules; and (C) instruments to effect staining or labeling of the biomolecules.
  • Figure 1 Demonstration of EtBr staining of DNA using two types coated backings.
  • Figure 1(a) shows an agarose gel stained with a backing comprising White Uncoated Paper #100.
  • Figure 1(b) shows an agarose gel stained with a backing comprising Prevail Paper #125. The gels were stained for 2-3 minutes and then placed on a Short Wave UV Transilluminator for visualization of the DNA bands and for obtaining photographs.
  • the present invention provides an article of manufacture and methods for safely staining or labeling biomolecules.
  • the stable, resilient and pliable article can be used repeatedly in a method for staining biomolecules in gels and membranes without directly contacting toxic staining solutions and without handling delicate gels which contain such stains.
  • the process eliminates the environmental hazard resulting from the disposal of toxic stains since the backing with the stain can be disposed of in a solid chemical waste container.
  • the process reduces the amount of stain to be used and eliminates the personal hazards associated with staining biomolecules since the operator will no longer have direct contact with the stain itself.
  • the article is easily manufactured which reduces the cost of the article and ensures its accessibility in the marketplace.
  • an article of manufacture which comprises a flexible backing and a dry coating adhered to a surface of the backing, wherein the coating comprises an indicator that stains or labels a biomolecule.
  • the backing is flexible, promotes good contact with a support or gel containing a biomolecule, is impermeable and allows the coating solution to be evenly spread and dried.
  • the backing can be composed of cellulose-based compounds, such as various papers, for example wall paper, cloth or vinyl, 3M WhatmanTM paper, vinyl paper, cloth paper, prepasted paper, to name a few.
  • the backing can be any wood, preferably light and strong as Balsam of about 1/16-1/8 of an inch in thickness, any glass such as borosilicate of about 50 mm, any cloth, cotton, rayon, tafetta, mesh, wool, synthetic polymers such as nylon, acetate, mixtures of cotton and acetate, polypropylene or polyethylene, polycarbonate, acrylic, cellophane acetate, Gelbond (FMC Bioproducts, Maine) to name a few, and any sponge.
  • the backing is comprised of two layers, consisting of a permeable layer and an impermeable layer.
  • the coating solution comprises an adhering solution and an indicator capable of staining or labeling a biomolecule.
  • Any solution which adheres to the backing and is preferably amenable to drying and rewetting, and does not degrade the biomolecule to be stained or the gel or support which retains the biomolecule to be stained can be utilized.
  • adhering solutions comprised of modified starches and their derivatives. Starch solutions can be modified in a variety of ways, including digestion with amylase.
  • Other examples of adhering solutions include, but are not limited to, water-based glues, flour, agarose, polyacrylamide and its derivatives, and any mixture there of.
  • glues include, but are not limited to, wall-paper glue, paper glue and multiple function glue.
  • Gums such as locust bean gum, also can be used. Adhering solutions containing silica or diatomaceous earth also are advantageous.
  • one or more indicators are entrapped in the adhering solution.
  • the desired indicator is mixed with the coating solution at varying amounts depending on the sensitivity of the stain.
  • the indicator can be in the form of a solution.
  • the indicator can be dissolved in water or a buffer. Suitable buffers can comprise mixtures of aqueous and organic solutions or comprise only organic solutions, such as isopropanol for ethidium bromide.
  • the indicator can be mixed into the coating solution as a powder.
  • the stain is spread onto a backing onto which a coating solution has been dried and which is capable of being rewetted again and redried.
  • indicators can be utilized individually or in combination in the present invention to stain or label biomolecules.
  • Preferred indicators include, but are not limited to, stains, dyes and labeled probes. Examples of acceptable stains and dyes include, but are not limited to, ethidium bromide, YoYo (Molecular Probes, Inc., Boulder, CO), Toto (Molecular Probes, inc.
  • the indicator comprises one or more probes complementary to the biomolecule to be detected.
  • a complementary probe include, but are not limited to, a labeled synthetic oligonucleotide, an antibody and antibody fragment.
  • probes can be added to the coating solution, or applied to the dried backing with the coating solution instead of, or in addition to, a stain.
  • the probe can be labeled with a radioactive label or a non-radioactive label such as biotin, alkaline phosphatase, and horseradish peroxidase, or a chemiluminescent reagent, among others.
  • the labeled probe can be added at a concentration of about 1 - 1000 pmol/ml, preferably about 100 pmol/ml.
  • compositions are added to the coating solution.
  • Such compositions for example tris acetate, polyethylene glycol and its derivatives, and triglycerol, can facilitate staining or can stabilize the stain or biomolecules.
  • Incorporating a hybridization buffer into the coating solution is especially useful when the indicator comprises a labeled probe.
  • the coating solution with an indicator can be spread onto one or both sides of the backing.
  • the backing can be spread with the coating solution, dried, and then coated with an indicator solution.
  • Coating and indicator solutions can be applied onto the backing by rolling them with a sponge roller or automated roller, or by brashing or spraying them onto the backing.
  • the coated backing can be air dried, oven dried, or dried in a microwave oven.
  • a method for staining biomolecules comprising applying an article of manufacture comprising a flexible backing and a dry coating adhered to a surface of the backing, wherein the coating comprises an indicator that stains or labels a biomolecule, to a gel or support containing the biomolecules for a sufficient period of time to allow diffusion to the biomolecules.
  • the coating comprises an indicator that stains or labels a biomolecule, to a gel or support containing the biomolecules for a sufficient period of time to allow diffusion to the biomolecules.
  • Usually, about 0.5 minute or longer of direct contact is required to allow the indicator to diffuse to the biomolecules.
  • biomolecules include, but are not limited to, DNA, RNA and proteins.
  • the present invention is used to stain or label biomolecules contained in gels.
  • a gel containing biomolecules can be made of any sieving material such as agarose, starch, polyacrylamide synthetic matrices, or various blends of matrices.
  • the backing is peeled off, and can be disposed of in the solid chemical waste, or reused.
  • a fresh application of the desired stain may be necessary upon reuse. This process prevents direct contact with toxic staining solutions, minimizes the volume of the staining solution utilized and saves the environment from any hazards which such a staining solution may produce.
  • the present invention is used to label biomolecules immobilized on a support.
  • Hybridization assays such as Southern, northern and western assays, utilize labeled probes to detect specific DNA, RNA or protein species immobilized onto membranes, such as nylon or nitrocellulose.
  • immobilized biomolecules may be detected using the method described above.
  • a probe for example a labeled synthetic oligonucleotide complementary to the biomolecule to be detected, is added to the coating solution, or applied to the dried backing with the coating solution.
  • the oligonucleotide can be labeled with a radioactive label or a non-radioactive label such as biotin, alkaline phosphatase, horseradish peroxidase or a chemiluminescent reagent among others.
  • a radioactive label or a non-radioactive label such as biotin, alkaline phosphatase, horseradish peroxidase or a chemiluminescent reagent among others.
  • the backing containing the labeled probe is applied to the membrane such that the probe is in direct contact with the support containing the biomolecules to be detected and even transfer of the probe from the backing to the biomolecules is effected.
  • the backing and the support are left in contact for several minutes up to eighteen hours or overnight. Detection of complementary binding between the labeled probe and the immobilized biomolecule may be carried out by methods known in the art.
  • the present invention provides a kit suitable for use in a method for staining or labeling biomolecules, the kit comprising an article of manufacture comprising a flexible backing and a dry coating adhered to a surface of the backing, wherein the coating comprises an indicator that stains or labels a biomolecule, reagents to effect staining or labeling of the biomolecules, and instruments to effect staining or labeling of the biomolecules.
  • the kit can be an educational or research kit, whereby other reagents for the preparation of the separation gels are included, as well as other reagents which facilitate detecting stained biomolecules, for example buffers, glycerol solutions or enzymes.
  • Instruments which facilitate staining or detecting biomolecules can be included in the kit.
  • a roller which can be used to promote effective contact between the backing and the gel or support containing the biomolecules can be included.
  • a cassette into which the backing and the gel or support are placed and which promotes effective contact between the two can be included in the kit.
  • a spray applicator which can be used to apply reagents effecting staining can be included.
  • a kit for staining biomolecules may be packaged in a variety of ways.
  • the coated backing When the kit contains a backing with a coating solution comprising ethidium bromide for staining DNA or RNA, the coated backing must be stored such that it is not exposed to light, since ethidium bromide is light sensitive.
  • a preferred package for this embodiment is a foil pouch. It is contemplated that a plurality of backing strips can be stored in a roll such that the desired size of backing can be cut away either using scissors or using a sharp serrated metal edge adhered to the box in which the roll is stored. Additionally, the use of perforated paper can simplify the dispensing process. In these forms, it is preferable that the coated backing be covered with a liner which when peeled away exposes the coating just prior to use so that the backings in the roll do not adhere to each other.
  • Such a liner can be made from paper or other release liner.
  • the backing can be stacked in sheets, folded and stored in a dispenser for easy removal of one sheet at a time.
  • the coating solution can be supplied in a separate container for application onto the backing when needed.
  • the coating solution can be supplied with or without stain, and the staining solution or powder can be provided in yet another container.
  • An adhering solution is prepared by forming a 10% solution of modified starch using warm, distilled water. An appropriate amount of ethidium bromide is then added to the adhering solution, preferably to a final concentration of between 0.05 mg/ml and 0.2 mg/ml. The resulting solution is spread over one side of a cellulose-based paper using a sponge roller and allowed to dry. After the coating solution has dried, the paper may be rolled up and stored until use.
  • Ethidium bromide was added to a final concentration of 0.0625 mg/ml.
  • the resulting coating solution was spread onto two types of paper backing, White Uncoated Paper #100 and Prevail Paper #125, using a sponge roller and allowed to air dry in the dark. Approximately 0.5 ml of the coating solution was applied to each backing. Following fractionation, the gels were inverted, and the coated backing was placed on the gel such that the ethidium bromide was in contact with the gel containing the DNA. The gels were stained for 2-3 minutes and then placed on a Short Wave Ultraviolet Transilluminator for visualization of the DNA bands.
  • the results in Figure 1 show that the present invention provides a safe and effective means of staining DNA molecules contained in gels.
  • Figure 1(a) is a photograph of a gel stained with the coated backing comprising White Uncoated Paper #100.
  • Figure 1(b) is a photograph of a gel stained with the coated backing comprising Prevail Paper #125.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Biotechnology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pathology (AREA)
  • Microbiology (AREA)
  • General Physics & Mathematics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Cell Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biophysics (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Paints Or Removers (AREA)

Abstract

Il est possible de marquer ou de colorer des biomolécules qui sont contenues dans des gels ou qui sont situées sur des membranes sans qu'il existe de contact direct avec les solutions toxiques de coloration, pour ce faire, on applique sur le gel ou sur la membrane un article manufacturé comprenant un support souple doté d'un revêtement contenant une coloration ou une marque. Pendant l'application, la coloration ou la marque est transférée du support sur les biomolécules, ceci ayant pour effet de marquer ces dernières. Le volume de solution de coloration utilisé dans cette technique est réduit au maximum, et les dangers pour l'environnement sont per conséquent réduits. De plus, la facilité de la fabrication réduit le coût de l'article.
PCT/US1999/003704 1998-02-19 1999-02-19 Articles manufactures et procedes de marquage de biomolecules Ceased WO1999042620A2 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP99908309A EP1057001A2 (fr) 1998-02-19 1999-02-19 Articles manufactures et procedes de marquage de biomolecules
CA002321100A CA2321100A1 (fr) 1998-02-19 1999-02-19 Articles manufactures et procedes de marquage de biomolecules
AU27771/99A AU2777199A (en) 1998-02-19 1999-02-19 Articles of manufacture and methods for staining biomolecules
JP2000532558A JP2002504351A (ja) 1998-02-19 1999-02-19 生体分子染色用製品及びその方法

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US7517398P 1998-02-19 1998-02-19
US60/075,173 1998-02-19

Publications (3)

Publication Number Publication Date
WO1999042620A2 true WO1999042620A2 (fr) 1999-08-26
WO1999042620A3 WO1999042620A3 (fr) 1999-11-18
WO1999042620A9 WO1999042620A9 (fr) 2000-03-02

Family

ID=22124035

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/003704 Ceased WO1999042620A2 (fr) 1998-02-19 1999-02-19 Articles manufactures et procedes de marquage de biomolecules

Country Status (5)

Country Link
EP (1) EP1057001A2 (fr)
JP (1) JP2002504351A (fr)
AU (1) AU2777199A (fr)
CA (1) CA2321100A1 (fr)
WO (1) WO1999042620A2 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005033342A1 (fr) 2003-09-30 2005-04-14 Molecular Probes, Inc. Detection d'acide nucleique immobilise
WO2007010532A3 (fr) * 2005-07-18 2008-01-10 Shmuel Bukshpan Compositions destinees a des analyses colorimetriques, et methodes d'utilisation des compositions

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005033342A1 (fr) 2003-09-30 2005-04-14 Molecular Probes, Inc. Detection d'acide nucleique immobilise
EP1988177A1 (fr) 2003-09-30 2008-11-05 Molecular Probes Inc. Détection d'acide nucléique immobilisé
US7727716B2 (en) 2003-09-30 2010-06-01 Life Technologies Corporation Detection of immobilized nucleic acid
US7977057B2 (en) 2003-09-30 2011-07-12 Life Technologies Corporation Detection of immobilized nucleic acid
US8969004B2 (en) 2003-09-30 2015-03-03 Life Technologies Corporation Detection of immobilized nucleic acid
WO2007010532A3 (fr) * 2005-07-18 2008-01-10 Shmuel Bukshpan Compositions destinees a des analyses colorimetriques, et methodes d'utilisation des compositions

Also Published As

Publication number Publication date
EP1057001A2 (fr) 2000-12-06
CA2321100A1 (fr) 1999-08-26
JP2002504351A (ja) 2002-02-12
WO1999042620A3 (fr) 1999-11-18
WO1999042620A9 (fr) 2000-03-02
AU2777199A (en) 1999-09-06

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