WO2001009591A9 - Verfahren zur optischen anregung von fluorophor-markieter dna und rna - Google Patents
Verfahren zur optischen anregung von fluorophor-markieter dna und rnaInfo
- Publication number
- WO2001009591A9 WO2001009591A9 PCT/EP2000/006546 EP0006546W WO0109591A9 WO 2001009591 A9 WO2001009591 A9 WO 2001009591A9 EP 0006546 W EP0006546 W EP 0006546W WO 0109591 A9 WO0109591 A9 WO 0109591A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- excitation
- fluorophores
- fluorescence
- fish
- fluorophore
- Prior art date
Links
Classifications
-
- 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
- C12Q1/6813—Hybridisation assays
- C12Q1/6841—In situ hybridisation
Definitions
- the invention relates to a method for the optical excitation of fluorophore-labeled DNA and of fluorophore-labeled RNA, in particular of specific localizations of DNA and RNA marked by fluorescence in situ hybridization (FISH).
- FISH fluorescence in situ hybridization
- the method is suitable for the excitation and spatially resolved detection of FISH-labeled chromosomal structures and enables the simultaneous excitation of several fluorophores. The method is therefore recommended for multi-gene detection.
- DAPI 4,6-diamidino-2-phenylindole hydrochloride
- Hoechst 33342 on the other hand by specifically binding fluorophores, which enable detection of small gene and chromosome areas as well as whole, special chromosomes.
- the fluorophore is coupled to the desired DNA region by fluorescence in situ hybridization (FISH).
- FISH fluorescence in situ hybridization
- a wide-ranging application of the FISH technique is given by the use of several fluorophores with different emission behavior for the localization of specific DNA areas, which thus enable multi-gene detection through "multi-color detection”.
- This special technique becomes multiplex -FISH, M-FISH or Multi-Color-FISH.
- different excitation wavelengths are used for the excitation of the different fluorophores.
- the latter emissions are, for example, staggered by filter wheels (non-simultaneous) or by special filters with transmission for several excitation wavelengths (e.g. Dan Pinkel filter) or a multi-line output of a laser (e.g. US Patent 5, 127,730) simultaneously (simultaneously
- filter wheels non-simultaneous
- special filters with transmission for several excitation wavelengths
- a multi-line output of a laser e.g. US Patent 5, 127,730
- a cytogenetic study of hu manen chromosomes often the UV emission of a light source, e.g. B.
- a mercury or xenon high-pressure lamp used for the fluorescence excitation of a non-specific DNA marker (also known as counterstain), as well as a blue emission of the light source for the excitation of a FISH fluorophore with fluorescence in the green area and the green emission of the light source for excitation of a FISH fluorophore with fluorescence in the red area.
- a three-dimensional representation (3D) with high spatial resolution is not possible with these non-coherent excitation sources.
- FISH fluorescence in situ hybridization
- 3 D images are taken with the blue / green excitation wavelengths of the argon ion laser at 488 nm and 514 nm and with the wavelengths 536 nm and 633 nm of the He-Ne laser.
- Such laser scanning microscopes usually have do not have an additional UV light source for the 3D excitation of the non-specific DNA markers Hoechst and DAPI.
- NIR near infrared
- Multiphoton excitations with NIR excitation radiation typically require light intensities of more than 100 MW / cm.
- Such high intensities can be achieved by means of continuously focussing (cw) lasers or pulsed lasers, preferably in the picosecond range and femtosecond range of moderate laser power through high focusing, e.g. B. by diffraction-limited focusing with high numerical aperture objectives can be achieved (e.g. Science 248 (1990), 73-76; Nature 377 (1995), 20-21; J. Microsc. 1 (1998), 28).
- cw continuously focussing
- the invention is based on the object of specifying a method which, with less effort, enables simultaneous, high-contrast excitation of several FISH fluorophores to be detected and represented in three dimensions with different fluorescence characteristics, and the excitation and detection of the fluorophores at a depth of more than 100 biological material Micrometers guaranteed and which does not have the disadvantages of previous methods listed above.
- the FISH fluorophores and the non-specific DNA markers with excitation rays are only of one wavelength in the range of 700 nm to 1000 nm excited, the radiation can be both unpulsed and pulsed and the light intensity in a spatially limited volume is more than 100 MW / cm.
- FISH fluorophores and non-specific DNA markers are efficient and rich in contrast as well could be stimulated to fluorescence with the possibility of a three-dimensional representation.
- the fluorescence maximum varied in a range from 480 nm to 650 nm and was therefore at least 150 nm away from the excitation wavelength.
- the separation of excitation photons and fluorescence photons was therefore not a problem and was achieved by using a simple short pass age, e.g. B. only radiation smaller than 700 nm, realized.
- the fluorophores were bound to human chromosomes.
- light excitation with the intense laser beam in the near infrared range is based on multi-photon excitation, in which two photons (two-photon excitation) or three photons (three-photon excitation) are absorbed simultaneously and each photon only one Provides a fraction of the energy required for a transition to the excited electronic state (see FIG. 1).
- multiphoton excitation in which two photons (two-photon excitation) or three photons (three-photon excitation) are simultaneously absorbed and each photon provides only a fraction of the energy required for a transition to the excited electronic state (see FIG. 1 ), is not known to the experts for the investigation of FISH fluorophores and DNA markers and for the implementation of a novel multiplex FISH display.
- the inventors were able to perform three-dimensional multiplex FISH images of human beings with the laser beam at both 770 nm and 800 nm Create fluorescence-labeled chromosomes after multiple FISH labeling with a lateral resolution of less than 500 nm and an axial resolution of less than 1000 nm without using pinholes.
- the sample was scanned by the high-intensity laser beam.
- the different fluorescences excited by the near infrared laser beam were displayed simultaneously using appropriate dichroic mirrors and broadband filters and with different detectors.
- the FISH fluorophores were first detected and then the DNA was labeled and detected with the fluorophore DAPI.
- Fig. 1 Schematic representation of a 1-, 2- and 3-photon absorption
- Fig. 2 triple fluorophore-labeled amniotic fluid cell with fluorescence excitation according to the invention
- 3 depth-resolved optical sections of a quadruple staining of the cell nuclei of two amniotic fluid cells excited in the NIR to fluoresce
- 1 shows the principle of action of the multiphoton-excited visible fluorescence with intensive near infrared laser radiation in comparison to a single-photon excitation. Two or three photons are absorbed simultaneously and together provide the necessary energy to occupy the required high-energy state from which the fluorescence emission originates.
- FIG. 2 shows depth-resolved images of a triple fluorophore-labeled amniotic fluid cell which was irradiated with NIR radiation of wavelength 770 nm for fluorescence.
- the non-specific DNA marker DAPI and the FISH fluorophores rhodamine (centromer of chromosome 18 marked) and FITC (centromer of chromosome 8 marked) were stimulated to produce visible fluorescence by means of a two-photon excitation.
- the appearance of three rhodamine hybridization signals indicates to the examined amniotic fluid cell that there is genetic damage in the form of a trisomy 18.
- the centromeres of chromosomes 8 and 18 are not in one plane, but can be localized with the possibility of 3D representation in the form of depth-resolved optical sections with an axial distance of 1 ⁇ m.
- FIG. 3 shows depth-resolved optical sections of a quadruple staining of the cell nuclei of two amniotic fluid cells with the FISH fluorophores
- Spectrum Aqua centromer of chromosome 18 marked
- Spectrum Green centromer of the X chromosome marked
- Spectrum Orange centromer of the Y chromosome marked
- Spectrum Aqua shows in Single-photon absorption spectrum and in the fluorescence spectrum bands at 433 nm and 480 nm, Spectrum Green at 509 nm and 538 nm, Spectrum Orange at 559 nm and 588 nm, and DAPI at 358 nm and 561 nm.
- the fluorescence images of the nuclei shown in FIG. 3 have red and green fluorescent FISH signals which indicate a female embryo.
- One of the cores also has three blue fluorescent signals that indicate a trisomy 18.
- the images, which were taken in different planes of the cell nucleus with an axial distance of 0.5 ⁇ m, show the spatial arrangement of the cell nuclei based on the DAPI fluorescence as well as the spatial position of the FISH-labeled centromeres in the approx.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00954464A EP1117985A1 (de) | 1999-07-29 | 2000-07-11 | Verfahren zur optischen anregung von fluorophor-markieter dna und rna |
JP2001514553A JP2003506677A (ja) | 1999-07-29 | 2000-07-11 | 蛍光体でマーキングしたdnaおよびrnaの光励起法 |
US09/806,375 US6528802B1 (en) | 1999-07-29 | 2000-07-11 | Method for optical excitation of fluorophore marked DNA and RNA |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19935766.8 | 1999-07-29 | ||
DE19935766A DE19935766A1 (de) | 1999-07-29 | 1999-07-29 | Verfahren zur optischen Anregung von Fluorophor-markierter DNA und RNA |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2001009591A1 WO2001009591A1 (de) | 2001-02-08 |
WO2001009591A9 true WO2001009591A9 (de) | 2002-09-06 |
Family
ID=7916558
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2000/006546 WO2001009591A1 (de) | 1999-07-29 | 2000-07-11 | Verfahren zur optischen anregung von fluorophor-markieter dna und rna |
Country Status (5)
Country | Link |
---|---|
US (1) | US6528802B1 (de) |
EP (1) | EP1117985A1 (de) |
JP (1) | JP2003506677A (de) |
DE (1) | DE19935766A1 (de) |
WO (1) | WO2001009591A1 (de) |
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EP2264428B1 (de) * | 1997-01-31 | 2017-05-03 | Xy, Llc | Optisches Gerät mit fokussierendem Reflektor zur Konvergenz von Strahlung auf einen Partikelfluss |
US6149867A (en) * | 1997-12-31 | 2000-11-21 | Xy, Inc. | Sheath fluids and collection systems for sex-specific cytometer sorting of sperm |
NZ527659A (en) | 1998-07-30 | 2006-02-24 | Colorado State University Thro | Equine artificial insemination when there has been sex selection of the sperm to produce an equine of the desired sex |
US7208265B1 (en) * | 1999-11-24 | 2007-04-24 | Xy, Inc. | Method of cryopreserving selected sperm cells |
DE10015448A1 (de) * | 2000-03-29 | 2001-10-11 | November Ag Molekulare Medizin | Verfahren zum Nachweisen und/oder Quantifizieren des Bindens erster Moleküle an dazu affine zweite Moleküle |
AR034121A1 (es) | 2000-05-09 | 2004-02-04 | Xy Inc | Metodo para aislar celulas de esperma que contienen cromosoma x de celulas de esperma que contienen cromosoma y |
JP2004503231A (ja) * | 2000-06-12 | 2004-02-05 | エックスワイ,インコーポレイテッド | X染色体保有精子およびy染色体保有精子の単離された集団を利用する統合群れ管理システム |
DE10035190C5 (de) * | 2000-07-20 | 2009-07-16 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Verfahren und Vorrichtung zur Fluoreszenzmessung |
AU2002220018A1 (en) | 2000-11-29 | 2002-06-11 | Colorado State University | System for in-vitro fertilization with spermatozoa separated into x-chromosome and y-chromosome bearing populations |
US7713687B2 (en) | 2000-11-29 | 2010-05-11 | Xy, Inc. | System to separate frozen-thawed spermatozoa into x-chromosome bearing and y-chromosome bearing populations |
JP4463473B2 (ja) * | 2000-12-15 | 2010-05-19 | ジ・アリゾナ・ボード・オブ・リージェンツ | 前駆体を含有するナノ粒子を用いた金属のパターニング方法 |
DE10065146A1 (de) * | 2000-12-22 | 2002-07-11 | Karsten Koenig | Verfahren und Anordnung zur nicht-invasiven dreidimensionalen optischen Untersuchung und Therapie der Haut |
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US20070096039A1 (en) * | 2002-05-03 | 2007-05-03 | Rakesh Kapoor | Evaluation Of Multicomponent Mixtures Using Modulated Light Beams |
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JP4521517B2 (ja) * | 2004-03-01 | 2010-08-11 | 独立行政法人産業技術総合研究所 | 微小対象物放出光検出装置 |
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US8323886B2 (en) * | 2004-06-18 | 2012-12-04 | Wlodek Mandecki | Fluorescence methods of detecting a protein-elongation related complex and corollary sequence information |
MX2007000888A (es) | 2004-07-22 | 2007-04-02 | Monsanto Technology Llc | Procedimiento para enriquecer una poblacion de celulas de esperma. |
US9040305B2 (en) | 2004-09-28 | 2015-05-26 | Singulex, Inc. | Method of analysis for determining a specific protein in blood samples using fluorescence spectrometry |
US8685711B2 (en) | 2004-09-28 | 2014-04-01 | Singulex, Inc. | Methods and compositions for highly sensitive detection of molecules |
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-
1999
- 1999-07-29 DE DE19935766A patent/DE19935766A1/de not_active Withdrawn
-
2000
- 2000-07-11 EP EP00954464A patent/EP1117985A1/de not_active Withdrawn
- 2000-07-11 US US09/806,375 patent/US6528802B1/en not_active Expired - Fee Related
- 2000-07-11 JP JP2001514553A patent/JP2003506677A/ja active Pending
- 2000-07-11 WO PCT/EP2000/006546 patent/WO2001009591A1/de not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JP2003506677A (ja) | 2003-02-18 |
DE19935766A1 (de) | 2001-02-01 |
EP1117985A1 (de) | 2001-07-25 |
US6528802B1 (en) | 2003-03-04 |
WO2001009591A1 (de) | 2001-02-08 |
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