CA2255952A1 - Nucleic acid sensor - Google Patents
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- CA2255952A1 CA2255952A1 CA002255952A CA2255952A CA2255952A1 CA 2255952 A1 CA2255952 A1 CA 2255952A1 CA 002255952 A CA002255952 A CA 002255952A CA 2255952 A CA2255952 A CA 2255952A CA 2255952 A1 CA2255952 A1 CA 2255952A1
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- 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
- C12Q1/6816—Hybridisation assays characterised by the detection means
- C12Q1/6825—Nucleic acid detection involving sensors
Abstract
The present invention provides biosensors and methods for the detection selected nucleic acid sequences. In one form the biosensor comprises an electrode and a bilayer membrane having a top and a bottom layer. The bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, with the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence. The membrane comprises a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer. The first half membrane spanning monomers are capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers are prevented from lateral diffusion within the bottom layer. A first ligand specifically reactive with the selected nucleic acid sequence is attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand reactive with the selected nucleic acid or marker attached thereto is attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane.
Description
Nucleic Acid Sensor FIELD OF INVENTION
The present invention relates to a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample and to a method of detecting the presence of a selected nucleic acid (NA) sequence in a sample.
BACKGROUND OF THE INVENTION
Assays for the presence of specific DNA or RNA sequences in samples have applications in many fields. For example, infection of patients with a particular microorganism can be assessed by analyzing a biological sample from the patient for the presence of a NA sequence specific for the microorganism. Other applications include the analysis of food or environmental samples to detect contamination. The detection of genetic disease caused by mutations can also be achieved by these techniques.
To date, the widespread use of this highly sensitive method has been restricted by the need for significant amplification of the amount of the specific nucleic acid sequence and/or the need to use specialized techniques to analyze the amplified DNA This amplification is generally achieved using polymerase chain or ligase chain reaction and the amplified DNA is then separated on a gel and the gel analyzed for the presence of specific bands of DNA.
Other methods include US 4,840,893, which teaches a method of nucleic acid detection. The method uses a probe sequence with attached ligand, an enzyme mediator system linked to a second ligand and which is capable of transferring a charge to an electrical surface when the enzyme is catalytically active, and an antiligand, to which the first and second ligands compete for binding. The assay is a competition system whereby the binding of the target sequence in a sample affects the availability of the first ligand and alters the rate of charge transfer to the electrode. The present invention has the advantage of providing a direct gating mechanism, which does not rely on a signal generated by enzyme catalysis.
U.S. 4,868,104 describes a method of detecting a nucleotide sequence by the use of two polynucleotide reagents, which bind to different sequences on the target analyte, the first of which can be polymerized and the second has a detection system. Several other patents describe nucleic acid detection methods, most of which involve labelling of the probes. These SUBSTITUTE SHEET (RULE 26) Z
include: U.S. 4,968,602; U.S. 5,116,733; U.S. 4,868,105; U.S. 4,716,106;
U.S. 4,883,750; U.S. 5,242,794; U.S. 4,996,142; U.S. 5,348,855 and U.S.
5,053,326.
BRIEF DESCRIPTION OF DRAWINGS
Figures 1 to 3 show the results obtained in Examples 1 to 3.
Fig. 4 shows linker gramicidin B
Fig. 5 shows membrane spanning lipid Fig. 6 shows linker lipid A
Fig. 7 shows biotinylated gramicidin E
DESCRIPTION OF THE INVENTION
The present inventors propose an apparatus which can be used to detect the presence of a specific NA sequence in a sample. The apparatus is best described as a biosensor in that it involves the use of lipid membranes.
Membranes for the use in biosensors have been disclosed In international Patent Application Nos PCT/AU88/00273, PCT/AU89/00352 PCT/AU90/00025 and PCT/AU92/00132. The disclosure of these applications is included herein by reference.
As disclosed in these applications, suitably modified lipid molecules may be caused to assemble into an electrode/ionic reservoir/insulating bilayer combination that is suitable for incorporation of ion channels and ionophores. It is also disclosed that the conductance of these membranes is dependent on the presence or absence of an analyte. In bilayer membranes in which each layer includes ion channel monomers, the conductance of the membrane is dependent on the lining up of the monomers in each layer to form continuous ion channels which span the membrane. As these continuous ion channels are constantly being formed and destroyed, the conductance of the membrane is dependent on the lifetimes of these continuous ion channels.
In a first aspect, the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand reactive with the selected nucleic acid or marker attached thereto is attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane.
In a preferred embodiment of the present invention the membrane includes membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane.
In a second aspect, the present invention consists in a biosensor for use in detecting the presence of a selected nucleic add sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer) the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand reactive with the selected nucleic acid or marker attached thereto attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or the end of the membrane-spanning amphiphiles proximal the surface of the membrane.
In a third aspect the present invention consists in a method of detecting the presence of a selected nucleic acid sequence within a sample, the method comprising adding the sample to the biosensor of the first or second aspect of the present invention and detecting change in the impedance or conductance of the membrane.
As will be understood by those of moderate skill in the art the biosensor and method of the present invention functions by the binding of the selected nucleic acid sequence to the first and second ligands causing a change in the ability of ions to traverse the membrane via the ion channels.
The specificity of the detection is provided by the specificity of the first iigand for the selected nucleic acid squence. This specifity may be provided in a number of ways, however, it is presently preferred that this is achieved by the use of first ligand which comprises a nucleic acid molecule or PNA
which includes a sequence complementary to a first sequence within the selected nucleic acid. As will be understood the sequence within the first ligand may be of any length sufficient to provide the required level of sensitivity, typically at least 10 residues. It will also be understood the nucleic acid molecule may include modified bases.
As the specificity is provided primarily by the first ligand it is not essential that the second ligand is specific for the selected nucleic acid sequence, it is simply necessary that the second ligand binds nucleic acid or a marker attached thereto. Accordingly) the second ligand may be an antibody directed against DNA, or binding fragment thereof. The second Iigand may also be an intercalating agent, major or minor groove binder or an agent capable of triple helix formation or an agent capable of covalently linking to nucleic acids upon activation or combinations thereof. It is preferred that the second ligand is not specific for the selected nucleic acid sequence as this results in simpler assembly of the biosensor as only one specific ligand need be produced for each selected nucleic acid sequence that is to be detected.
The biosensor may also include a variety of second ligands which vary over the biosensor. For example the second ligand attached to one membrane spanning amphiphile may be a different moiety to the second ligand attached to another membrane spanning amphiphile. The essential feature is that the second ligand binds to nucleic acid or to a marker attached thereto. Accordingly, it is to be understood that the term "second ligand"
embraces a single or multiple species of moieties which bind nucleic acid or 5 to a marker attached thereto.
As will appreciated by those skilled in the field in a number of applications the nucleic acid sequence to be detected will be labelled with a marker, for example a biotinylated PCR product.
It is, however, also clearly within the ambit of the present invention that both the first and second ligands are specific for the selected nucleic acid sequence. In such an embodiment the first and second ligands are specific for different sequences within the selected nucleic acid sequence.
The first and second ligands may be attached in any of a number of ways. For example, streptavidin may be attached as described in the applications setout above. This can then be used to bind biotinylated nucleic acid. It is preferred that the first and second ligands are attached via linkers to the ion channels or membrane spanning lipids. Where a linker is used it is preferred that the linker is hydrophilic. It is further preferred that the linker includes a phosphoramidite group.
It is also expected that changing the linker length may affect the gating response detected in the biosensor.
Where the first and second ligands are nucleic acid sequences this may be advantageously achieved by producing a molecule having the two DNA sequences which are to act as the ligands at each end with an RNA
sequence in the middle. The two ends of the molecule are then attached to the biosensor surface and the central RNA portion digested with RNaseH to leave the biosensor with the two separated DNA sequences attached.
In a preferred embodiment the first ligand comprises a nucleic acid molecule which includes a sequence complementary to a first sequence within the selected nucleic acid. It is further preferred that the second ligand comprises a nucleic acid molecule which includes a sequence complementary to a second sequence within the selected nucleic acid. Due to the presence of such complementary sequences the first and second ligands bind to the selected nucleic acid by hydridisation.
It is presently preferred that the first and second ligands are oligonucleotide sequences selected to bind to different regions of the selected nucleic acid sequence in the sample. Methods to detect or sense specific NA
sequences using the impedance bridge described in International Patent Application Nos PCT/AU88/00273, PCT/AU88/00273, PCT/AU89/00352, PCT/AU90/00025 and PCT/AU92/00132, may, for example, be achieved by manufacturing the membrane with both biotinylated membrane spanning lipids (MSL) and biotinylated gramicidin. Streptavidin, which binds strongly to biotin is immobilized by reaction with these biotinylated compounds.
A mixture of two biotinylated oligonucleotide sequences (first and second ligands) .are then attached to the streptavidin. These sequences are preferably non complementary. One sequence would be a suitable probe for a sequence of interest e.g., an infectious organism probe sequence, and the other sequence would be the complement to another part of the target DNA.
Upon addition of the DNA to be detected, cross linking of the two biotinylated sequences occurs if the DNA contains the sequences which hybridise to the two attached sequences but not otherwise.
In a fourth aspect the present invention consists in a method of detecting the presence of a selected nucleic acid within a sample, the method comprising the following steps:
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom Layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with a first nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane, either the first or second nucleic acid sequence being within the sequence of a selected nucleic acid;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
If the target nucleic acid is present in the sample, the challenge sequence is unable to bind to both the first and second ligands and thus, crosslink. An absence of a difference in the conductance/impedance measurements in (ii) and (iii) being indicative of the presence of the selected nucleic acid sequence in the sample.
in a fifth aspect the present invention consists in a method of detecting the presence of a selected nucleic acid sequence within a sample, the method comprising the following steps:
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to the other of the at least a proportion of the first half membrane-s spanning monomers proximal the surface of the membrane or an end of the membrane-spanning amphiphiles proximal the surface of the membrane;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
If the target nucleic acid is present in the sample, the challenge sequence is unable to bind to both the first and second ligands and thus, crosslink. An absence of a difference in the conductance/impedance measurements in (ii) and (iii) being indicative of the presence of the selected nucleic acid sequence in the sample.
In a sixth aspect the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane, the second ligand having bound thereto or included therein the selected nucleic acid sequence such that the first ligands binds to the second ligand.
In a seventh aspect the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or the end of the membrane-spanning amphiphiles proximal the surface of the membrane, the second ligand having bound thereto or included therein the selected nucleic acid sequence such that the first ligands binds to the second ligand.
In the arrangements specified in the sixth and seventh aspects the biosensor detects the presence of the selected nucleic acid sequence by competition. The selected nucleic acid sequence, if present in sample to be tested, competes with the second ligand for binding to the first ligand.
In an eighth aspect the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules 5 and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral 10 diffusion within the bottom layer and a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane.
In this arrangement upon addition of sample containing the selected nucleic acid sequence the first ligand will bind to the selected DNA sequence and change the mobility of the first half membrane monomers or restrict ion flow through the channel. This will result in a membrane with a different conductance.
In another preferred embodiment of the invention, the first and second half membrane spanning monomers are gramicidin or one of its derivatives.
In a further preferred embodiment of the present invention, the bilayer membrane is attached to the electrode via linking molecules such that a space exists between the membrane and the electrode. Preferred linking molecules are those disclosed in application PCT/AU92/00132. In yet a further preferred embodiment of the present invention, the second half membrane spanning monomers are attached to the electrode via linker groups.
In yet another preferred embodiment of the present invention, the bilayer membrane includes membrane spanning lipids, similar to those found in archaebacteria.
"Cross linking" is characterized by the cross linking sequence bringing the first half membrane spanning monomers out of alignment with the second half membrane spanning monomers. This results in a membrane having a second conductance which is different from the first conductance.
This difference in conductance can be measured and will be indicative of the presence of the selected DNA sequence in the sample.
The first and second ligands may be the same or different.
Oligonucleotide ligands which bind to specific NA sequences are well known in the art.
In an alterative embodiment of the present invention the ligands are peptide nucleic acids (PNA). Information regarding PNA may be found in Science, 1991, 254, 1497 1500; J. Am. Chem. Soc., 1992, 114, 1895 1897, J.
Am. Chem. Soc., 1992, 114, 9677 78; J. Chem. Soc. Chem. Commun., 1993, 800 801. Nature, 1993, 365, 566, 68; US Patent No. 4,795,700 and International Patent Application No. WO 93/18187 and the disclosure of these documents is included herein by reference. There are a number of advantages gained by the use of PNA as the ligands. These include the ability of PNA to recognize specific sequences in double stranded DNA and to bind thereto either by strand displacement or triple helix formation. This is in contrast-to oligonucleotides which can bind single strand or double strand but not by strand displacement. It should be noted that PNA can also bind to single stranded DNA. The target probe sequence could be a PNA
molecule for tighter binding.
In an alterative embodiment, a mixture of two biotinylated oligonucleotide sequences are immobilized onto streptavidin. One is the target probe sequence and the second is any appropriate cross linking sequence of choice. On addition of sample, the target analyte is captured.
The target analyte need only have the sequence of interest. No cross linking occurs, therefore gating is not observed and a first measurement of conductance is taken. A second oligonucleotide sequence is then used to challenge the system. This challenge sequence contains both the target oligonucleotide sequence and the complementary sequence to the cross linking sequence. If binding of both epitopes occurs, cross linking will take place, thus gating off the ion channels and changing the conductance of the membrane. If binding of only epitope two occurs (owing to the binding of the target DNA to its probe sequence) no cross linking takes place, thus no gating is seen. An absence of a change in conductance following addition of the challenge sequence is therefor an indication of the presence of the target analyte.
The NA probe sequence, in principle, can be of any length and will contain the base sequence complementary to the target analyte for detection.
The target analyte can be a DNA or an RNA sequence. A PNA probe sequence may also be of any length and will contain the base sequence complementary to the target analyte for detection. The target analyte can be a DNA or an RNA sequence as PNA binds to both. PNA binds DNA and RNA
more tightly than does DNA, therefore the challenge sequence should not be able to displace the already bound target sequence.
Some examples of target sequences are listed below.
Listeria monocytogenes; a 19 base pair oligonucleotide that is specific for a 36S rRNA sequence; detection in food industry (milks, cheeses etc.) See: R. F. Wang W. W. Cao and M.G. Johnson, App. Environ.
Microbiol., 1991, 3666 - 70.
A11 cholera toxin producing Strains of Vibrio cholerea c hybridise specifically with a 23 base pair oligonucleotide sequence (water detection, health). See: A C. Wright et al., J. Clin. Microbiol., 1992, 2302.
Specific oligonucleotide probes for detection of various strains of Chiamydia and Gonorrhoea (health industry). See: R. Rossau et al, u. Clin. Microbiol., 1990, 944 8; J. Gen. Microbiol, 1989, 135, 1735 45; Loeffelholz, M. J, J. Clin. Microbiol., 1992,2847 51.
An excellent summary of current technologies that use DNA probes is found In "DNA Probes", 2nd Ed.: G. H Keller & M. M. Manak, Stockton Press, 1993.
In order that the nature of the present invention may be more clearly understood preferred forms thereof will now be described with reference to the following non-limiting examples.
Example 1: Lateral Segregation of DNA
Detection of target polynucleotide sequences can be illustrated by the following example in which specific DNA gating is observed for a target DNA
concentration of 5 nM (1 pmole). The total lack of any response in the presence of a non-complementary probe sequence can be seen in the controls.
1st layer: 9.3nM Linker Gramicidin B
1.1M Membrane spanner Lipid D
27.5nM Membrane spanner Lipid C
37M dithio diglyconic acid 75M Linker Lipid A
2nd layer: l4mM (DPE-PC:GDPE=7:3) : Biotinylated Gramicidin E =
50,000:1 in ethanol Electrodes with freshly evaporated gold (1000A) on chrome adhesion layer (200A) on glass microscope slides) were dipped into an ethanolic solution of the first layer components for 1 hr at room temperature, rinsed with ethanol, then stored at 4~C under ethanol until used for impedance measurements. The slide was clamped into a block containing teflon coated wells which defined the area of the working electrode as approximately l6mmZ.
A11 steps were carried out at room temperature. 5~L of the 2nd layer was added to the working electrode before addition of a 180L volume of phosphate buffered saline (lOmM NaZHP04, 1mM KHZP04, 137mM NaCI, 2.7mM KCI, PBS). The electrode was washed 4 times using PBS.
Streptavidin was added to a11 wells (5~L 0.01mg/mL in PBS) and allowed to react with biotinylated Gramicidin E for 10-15 minutes before washing out excess unbound streptavidin with PBS. 5~L of a 1:1 mixture of DNA probe F
(200nM):DNA probe G (200nM in PBS) was added to sensor wells. A DNA
non-specific binding probe H (5~L 400 nM in PBS) was added to control wells. The probes were allowed to react with streptavidin for 10-15 minutes then excess unbound probes were washed out with PBS. 100~tL of DNA
target I (lOnM) in PBS was added to each well. The binding of DNA target I
to the sensor wells gave a decrease in the admittance at minimum phase, but no significant change in membrane admittance in control wells (Figure 1).
The amount and rate of decrease of admittance at minimum phase is related to the amount of DNA present in the test solution and therefore can be used to determine concentration in test solutions.
DNA probe F:
5'biotinylated listeria probe DNA with a 31-atom phosphoramidite linker group between the biotin and DNA.
5'-bio-L-M-ATAGTTTTATGGGATTAGC-3' DNA probe G:
5'biotinylated cholera toxin probe DNA with a 31-atom phosphoramidite linker group between the biotin and DNA.
5'-bio-L-M-CTCCGGAGCATAGAGCTTGGAGG-3' DNA non-specific binding probe H:
5'biotinylated 15-mer oligonucleotide with a 31-atom phosphoramidite linker group between the biotin and DNA, which is non-complementary to all parts of the target DNA sequence.
5'-bio-L-M-ATTGCTACGTATACG-3' DNA target I:
67 base DNA sequence containing the 19-base listeria sequence, a 10 base 'spacer' and the 23 base cholera toxin sequence.
5'-GCTAATCCCATAA.A.ACTATGCATGCATGCATCGTACGTACGTA
CCCTCCAAGCTCTATGCTCCGGAG-3' where:
bio = biotin L=
O
O-DMT
O-P-O
II
O
WO 97/44651 PCTlAU97/00316 M=
o~
-o~o~o~o'~o~~'~o-P=o 5 Example Z: Lateral Segregation of DNA followed by enzymatic cleavage This example illustrates the ability to perform a second, confirmatory step whereby an enzyme can be used to cleave the bound polynucleotide, thus confirming that a specific region of interest is present.
1st layer: 9.3nM Linker Gramicidin B
l.luM Membrane spanner Lipid D
27.5nM Membrane spanner Lipid C
37uM dithio diglyconic acid 75uM Linker Lipid A
2nd layer: l4mM (DPE-PC:GDPE=7:3) : Biotinylated Gramicidin E =
50,000:1 in ethanol Electrodes were prepared and 2nd layer added as described in Example 1.
Subsequent streptavidin, DNA probe and DNA target sequences were added as described in Example 1, except that they were carried out at 30~C.
After 15 minutesof DNA gating, unbound DNA target I was washed out with DNase I activation buffer. DNase I activation buffer consists of 50 nM
Tris.HCl, pH 7.6, 50 nM NaCI, 10 nM MgClZ, 10 nM MnClz, 0.2 mg/mL BSA.
DNase I was added (2 yL 1mg/mL in a 50%W~~ glycerol solution of 20 mM
Tris.HCl, pH 7.6, 1 mM MgClz) to sensor and control wells. Addition of DNase I gave an increase in admittance at minimum phase for sensor wells, but no significant increase for control wells (figure 2), showing that cleavage of DNA was being detected.
Example 3: DNA gating by addition of 2 biotinylated complementary polynucleotide sequences This example illustrates the possibility of detecting only one specific sequence on the polynucleotide of interest by having a capture molecule incorporated in the target. It also illustrates the use of peptide nucleic acid (PNA) sequences.
1st layer: 9.3nM Linker Gramicidin B
l.luM Membrane spanner Lipid D
5.5nM Membrane spanner Lipid C
37uM dithio diglyconic acid 75uM Linker Lipid A
2nd layer: l4mM (DPE-PC:GDPE=7:3) : Biotinylated Gramicidin E =
50,000:1 in ethanol Electrodes were prepared and 2nd layer added as described in Example 1. All steps were carried out at room temperature. 5~L of the 2nd layer was added to the working electrode before addition of a 180L volume of phosphate buffered saline (lOmM Na2HP0~, 1mM KHZP04, 137mM NaCI, 2.7mM KCl, PBS). The electrode was washed 4 times using PBS.
Streptavidin was added to all wells (5~L 0.01mg/mL in PBS) and allowed to react with biotinylated Gramicidin E for 10-15 minutes before washing out excess unbound streptavidin with PBS.
5 nM of each of PNA sequence J and the complementary DNA
sequence K (1.14,L 1.75 ~M) were added quickly in succession to the sensor wells. No PNA or DNA sequence was added to the control wells. The binding of the PNA (J) and DNA (K) sequences to the streptavidin and each other gave a decrease in the admittance at minimum phase, but no significant change in membrane admittance in control wells (Figure 3). The amount and rate of decrease of admittance at minimum phase is related to the amount of DNA or PNA present in the test solution and therefore can be used to determine concentration in test solutions.
PNA sequence J:
N-biotinylated listeria probe sequence PNA containing glycine and lysine for solubility plus an 8-amino-3,6-dioxaoctanoic acid linker.
N-bio-gly-lys-O-ATAGTTTTATGGGATTAGC-CONHz DNA sequence K:
5'-biotinylated listeria DNA with no linker group between the biotin and DNA.
5'-bio-GCTAATCCCATAAAACTAT-3' where O=
o H
N.
~~O
It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in ZO the specific embodiments without departing from the spirit or scope of the invention as broadly described. These include the detection of PCR (or other amplification method) products and the detection of genetic mutations in genetically derived diseases, where the mutation is known. A list of some 3500 conditions due to defective genes can be found in McKusick's "Mendelian Inheritance in Man" and further examples are regularly reported in the scientific press. The present embodiments are, therefore, to be considered in a11 respects as illustrative and not restrictive.
17a SEQUENCE LISTING
(1) GENERAL INFORMATION:
(i) APPLICANT:
(A) NAME: Australian Membrane and Biotechnology Research Institute (B) STREET: 126 Greville St (C) CITY: Chatswood (D) STATE: New South Wales (E) COUNTRY: Australia (F) POSTAL CODE (ZIP): 2067 (A) NAME: The University of Sydney (C) CITY: Sydney (D) STATE: New South Wales (E) COUNTRY: Australia (F) POSTAL CODE (ZIP): 2006 (ii) TITLE OF INVENTION: Nucleic acid sensor (iii) NUMBER OF SEQUENCES: 6 (iv) CORRESPONDENCE ADDRESS:
(A) ADDRESSEE: SWABEY OGILVY RENAULT
(B) STREET: Suite 1600, l981 McGill College Avenue (C) CITY: Montreal (D) STATE: QC
(E) COUNTRY: Canada (F) ZIP: H3A 2Y3 (v) COMPUTER READABLE FORM:
(A) MEDIUM TYPE: Floppy disk (B) COMPUTER: IBM PC compatible (C) OPERATING SYSTEM: PC-DOS/MS-DOS
(D) SOFTWARE: PatentIn Release #1.0, Version #1.30 (EPO) (vi) CURRENT APPLICATION DATA:
(A) APPLICATION NUMBER: 2,255,952 (B) FILING DATE: 22-MAY-1997 (C) CLASSIFICATION:
(vi) PRIOR APPLICATION DATA:
(A) APPLICATION NUMBER: PCT/AU97/00316 (B) FILING DATE: 22-MAY-1997 (vi) PRIOR APPLICATION DATA:
(A) APPLICATION NUMBER: 60/018,125 (B) FILING DATE: 22-MAY-1996 (viii) ATTORNEY/AGENT INFORMATION:
(A) NAME: Cote, France (B) REGISTRATION NUMBER: 4166 (C) REFERENCE/DOCKET NUMBER: 3650-97 FC/ntb (ix) TELECOMMUNICATION INFORMATION:
(A) TELEPHONE: 514-845-7126 (B) TELEFAX: 514-288-B389 17b (C) TELEX:
(2) INFORMATION FOR SEQ ID NO: 1:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 19 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID N0: 1:
atagttttat gggattagc 19 (2) INFORMATION FOR SEQ ID NO: 2:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 23 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 2:
ctccggagca tagagcttgg agg 23 (2) INFORMATION FOR SEQ ID NO: 3:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 15 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 3:
attgctacgt atacg 15 (2) INFORMATION FOR SEQ ID NO: 4:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 67 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide 17c (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 4:
gctaatccca taaaactatg catgcatgca tcgtacgtac gtaccctcca agctctatgc 60 tccggag 67 (2) INFORMATION FOR SEQ ID N0: 5:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 19 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 5:
atagttttat gggattagc 19 (2) INFORMATION FOR SEQ ID NO: 6:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 19 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 6:
gctaatccca taaaactat 19
The present invention relates to a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample and to a method of detecting the presence of a selected nucleic acid (NA) sequence in a sample.
BACKGROUND OF THE INVENTION
Assays for the presence of specific DNA or RNA sequences in samples have applications in many fields. For example, infection of patients with a particular microorganism can be assessed by analyzing a biological sample from the patient for the presence of a NA sequence specific for the microorganism. Other applications include the analysis of food or environmental samples to detect contamination. The detection of genetic disease caused by mutations can also be achieved by these techniques.
To date, the widespread use of this highly sensitive method has been restricted by the need for significant amplification of the amount of the specific nucleic acid sequence and/or the need to use specialized techniques to analyze the amplified DNA This amplification is generally achieved using polymerase chain or ligase chain reaction and the amplified DNA is then separated on a gel and the gel analyzed for the presence of specific bands of DNA.
Other methods include US 4,840,893, which teaches a method of nucleic acid detection. The method uses a probe sequence with attached ligand, an enzyme mediator system linked to a second ligand and which is capable of transferring a charge to an electrical surface when the enzyme is catalytically active, and an antiligand, to which the first and second ligands compete for binding. The assay is a competition system whereby the binding of the target sequence in a sample affects the availability of the first ligand and alters the rate of charge transfer to the electrode. The present invention has the advantage of providing a direct gating mechanism, which does not rely on a signal generated by enzyme catalysis.
U.S. 4,868,104 describes a method of detecting a nucleotide sequence by the use of two polynucleotide reagents, which bind to different sequences on the target analyte, the first of which can be polymerized and the second has a detection system. Several other patents describe nucleic acid detection methods, most of which involve labelling of the probes. These SUBSTITUTE SHEET (RULE 26) Z
include: U.S. 4,968,602; U.S. 5,116,733; U.S. 4,868,105; U.S. 4,716,106;
U.S. 4,883,750; U.S. 5,242,794; U.S. 4,996,142; U.S. 5,348,855 and U.S.
5,053,326.
BRIEF DESCRIPTION OF DRAWINGS
Figures 1 to 3 show the results obtained in Examples 1 to 3.
Fig. 4 shows linker gramicidin B
Fig. 5 shows membrane spanning lipid Fig. 6 shows linker lipid A
Fig. 7 shows biotinylated gramicidin E
DESCRIPTION OF THE INVENTION
The present inventors propose an apparatus which can be used to detect the presence of a specific NA sequence in a sample. The apparatus is best described as a biosensor in that it involves the use of lipid membranes.
Membranes for the use in biosensors have been disclosed In international Patent Application Nos PCT/AU88/00273, PCT/AU89/00352 PCT/AU90/00025 and PCT/AU92/00132. The disclosure of these applications is included herein by reference.
As disclosed in these applications, suitably modified lipid molecules may be caused to assemble into an electrode/ionic reservoir/insulating bilayer combination that is suitable for incorporation of ion channels and ionophores. It is also disclosed that the conductance of these membranes is dependent on the presence or absence of an analyte. In bilayer membranes in which each layer includes ion channel monomers, the conductance of the membrane is dependent on the lining up of the monomers in each layer to form continuous ion channels which span the membrane. As these continuous ion channels are constantly being formed and destroyed, the conductance of the membrane is dependent on the lifetimes of these continuous ion channels.
In a first aspect, the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand reactive with the selected nucleic acid or marker attached thereto is attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane.
In a preferred embodiment of the present invention the membrane includes membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane.
In a second aspect, the present invention consists in a biosensor for use in detecting the presence of a selected nucleic add sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer) the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand reactive with the selected nucleic acid or marker attached thereto attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or the end of the membrane-spanning amphiphiles proximal the surface of the membrane.
In a third aspect the present invention consists in a method of detecting the presence of a selected nucleic acid sequence within a sample, the method comprising adding the sample to the biosensor of the first or second aspect of the present invention and detecting change in the impedance or conductance of the membrane.
As will be understood by those of moderate skill in the art the biosensor and method of the present invention functions by the binding of the selected nucleic acid sequence to the first and second ligands causing a change in the ability of ions to traverse the membrane via the ion channels.
The specificity of the detection is provided by the specificity of the first iigand for the selected nucleic acid squence. This specifity may be provided in a number of ways, however, it is presently preferred that this is achieved by the use of first ligand which comprises a nucleic acid molecule or PNA
which includes a sequence complementary to a first sequence within the selected nucleic acid. As will be understood the sequence within the first ligand may be of any length sufficient to provide the required level of sensitivity, typically at least 10 residues. It will also be understood the nucleic acid molecule may include modified bases.
As the specificity is provided primarily by the first ligand it is not essential that the second ligand is specific for the selected nucleic acid sequence, it is simply necessary that the second ligand binds nucleic acid or a marker attached thereto. Accordingly) the second ligand may be an antibody directed against DNA, or binding fragment thereof. The second Iigand may also be an intercalating agent, major or minor groove binder or an agent capable of triple helix formation or an agent capable of covalently linking to nucleic acids upon activation or combinations thereof. It is preferred that the second ligand is not specific for the selected nucleic acid sequence as this results in simpler assembly of the biosensor as only one specific ligand need be produced for each selected nucleic acid sequence that is to be detected.
The biosensor may also include a variety of second ligands which vary over the biosensor. For example the second ligand attached to one membrane spanning amphiphile may be a different moiety to the second ligand attached to another membrane spanning amphiphile. The essential feature is that the second ligand binds to nucleic acid or to a marker attached thereto. Accordingly, it is to be understood that the term "second ligand"
embraces a single or multiple species of moieties which bind nucleic acid or 5 to a marker attached thereto.
As will appreciated by those skilled in the field in a number of applications the nucleic acid sequence to be detected will be labelled with a marker, for example a biotinylated PCR product.
It is, however, also clearly within the ambit of the present invention that both the first and second ligands are specific for the selected nucleic acid sequence. In such an embodiment the first and second ligands are specific for different sequences within the selected nucleic acid sequence.
The first and second ligands may be attached in any of a number of ways. For example, streptavidin may be attached as described in the applications setout above. This can then be used to bind biotinylated nucleic acid. It is preferred that the first and second ligands are attached via linkers to the ion channels or membrane spanning lipids. Where a linker is used it is preferred that the linker is hydrophilic. It is further preferred that the linker includes a phosphoramidite group.
It is also expected that changing the linker length may affect the gating response detected in the biosensor.
Where the first and second ligands are nucleic acid sequences this may be advantageously achieved by producing a molecule having the two DNA sequences which are to act as the ligands at each end with an RNA
sequence in the middle. The two ends of the molecule are then attached to the biosensor surface and the central RNA portion digested with RNaseH to leave the biosensor with the two separated DNA sequences attached.
In a preferred embodiment the first ligand comprises a nucleic acid molecule which includes a sequence complementary to a first sequence within the selected nucleic acid. It is further preferred that the second ligand comprises a nucleic acid molecule which includes a sequence complementary to a second sequence within the selected nucleic acid. Due to the presence of such complementary sequences the first and second ligands bind to the selected nucleic acid by hydridisation.
It is presently preferred that the first and second ligands are oligonucleotide sequences selected to bind to different regions of the selected nucleic acid sequence in the sample. Methods to detect or sense specific NA
sequences using the impedance bridge described in International Patent Application Nos PCT/AU88/00273, PCT/AU88/00273, PCT/AU89/00352, PCT/AU90/00025 and PCT/AU92/00132, may, for example, be achieved by manufacturing the membrane with both biotinylated membrane spanning lipids (MSL) and biotinylated gramicidin. Streptavidin, which binds strongly to biotin is immobilized by reaction with these biotinylated compounds.
A mixture of two biotinylated oligonucleotide sequences (first and second ligands) .are then attached to the streptavidin. These sequences are preferably non complementary. One sequence would be a suitable probe for a sequence of interest e.g., an infectious organism probe sequence, and the other sequence would be the complement to another part of the target DNA.
Upon addition of the DNA to be detected, cross linking of the two biotinylated sequences occurs if the DNA contains the sequences which hybridise to the two attached sequences but not otherwise.
In a fourth aspect the present invention consists in a method of detecting the presence of a selected nucleic acid within a sample, the method comprising the following steps:
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom Layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with a first nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane, either the first or second nucleic acid sequence being within the sequence of a selected nucleic acid;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
If the target nucleic acid is present in the sample, the challenge sequence is unable to bind to both the first and second ligands and thus, crosslink. An absence of a difference in the conductance/impedance measurements in (ii) and (iii) being indicative of the presence of the selected nucleic acid sequence in the sample.
in a fifth aspect the present invention consists in a method of detecting the presence of a selected nucleic acid sequence within a sample, the method comprising the following steps:
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to the other of the at least a proportion of the first half membrane-s spanning monomers proximal the surface of the membrane or an end of the membrane-spanning amphiphiles proximal the surface of the membrane;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
If the target nucleic acid is present in the sample, the challenge sequence is unable to bind to both the first and second ligands and thus, crosslink. An absence of a difference in the conductance/impedance measurements in (ii) and (iii) being indicative of the presence of the selected nucleic acid sequence in the sample.
In a sixth aspect the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane, the second ligand having bound thereto or included therein the selected nucleic acid sequence such that the first ligands binds to the second ligand.
In a seventh aspect the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or the end of the membrane-spanning amphiphiles proximal the surface of the membrane, the second ligand having bound thereto or included therein the selected nucleic acid sequence such that the first ligands binds to the second ligand.
In the arrangements specified in the sixth and seventh aspects the biosensor detects the presence of the selected nucleic acid sequence by competition. The selected nucleic acid sequence, if present in sample to be tested, competes with the second ligand for binding to the first ligand.
In an eighth aspect the present invention consists in a biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules 5 and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral 10 diffusion within the bottom layer and a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane.
In this arrangement upon addition of sample containing the selected nucleic acid sequence the first ligand will bind to the selected DNA sequence and change the mobility of the first half membrane monomers or restrict ion flow through the channel. This will result in a membrane with a different conductance.
In another preferred embodiment of the invention, the first and second half membrane spanning monomers are gramicidin or one of its derivatives.
In a further preferred embodiment of the present invention, the bilayer membrane is attached to the electrode via linking molecules such that a space exists between the membrane and the electrode. Preferred linking molecules are those disclosed in application PCT/AU92/00132. In yet a further preferred embodiment of the present invention, the second half membrane spanning monomers are attached to the electrode via linker groups.
In yet another preferred embodiment of the present invention, the bilayer membrane includes membrane spanning lipids, similar to those found in archaebacteria.
"Cross linking" is characterized by the cross linking sequence bringing the first half membrane spanning monomers out of alignment with the second half membrane spanning monomers. This results in a membrane having a second conductance which is different from the first conductance.
This difference in conductance can be measured and will be indicative of the presence of the selected DNA sequence in the sample.
The first and second ligands may be the same or different.
Oligonucleotide ligands which bind to specific NA sequences are well known in the art.
In an alterative embodiment of the present invention the ligands are peptide nucleic acids (PNA). Information regarding PNA may be found in Science, 1991, 254, 1497 1500; J. Am. Chem. Soc., 1992, 114, 1895 1897, J.
Am. Chem. Soc., 1992, 114, 9677 78; J. Chem. Soc. Chem. Commun., 1993, 800 801. Nature, 1993, 365, 566, 68; US Patent No. 4,795,700 and International Patent Application No. WO 93/18187 and the disclosure of these documents is included herein by reference. There are a number of advantages gained by the use of PNA as the ligands. These include the ability of PNA to recognize specific sequences in double stranded DNA and to bind thereto either by strand displacement or triple helix formation. This is in contrast-to oligonucleotides which can bind single strand or double strand but not by strand displacement. It should be noted that PNA can also bind to single stranded DNA. The target probe sequence could be a PNA
molecule for tighter binding.
In an alterative embodiment, a mixture of two biotinylated oligonucleotide sequences are immobilized onto streptavidin. One is the target probe sequence and the second is any appropriate cross linking sequence of choice. On addition of sample, the target analyte is captured.
The target analyte need only have the sequence of interest. No cross linking occurs, therefore gating is not observed and a first measurement of conductance is taken. A second oligonucleotide sequence is then used to challenge the system. This challenge sequence contains both the target oligonucleotide sequence and the complementary sequence to the cross linking sequence. If binding of both epitopes occurs, cross linking will take place, thus gating off the ion channels and changing the conductance of the membrane. If binding of only epitope two occurs (owing to the binding of the target DNA to its probe sequence) no cross linking takes place, thus no gating is seen. An absence of a change in conductance following addition of the challenge sequence is therefor an indication of the presence of the target analyte.
The NA probe sequence, in principle, can be of any length and will contain the base sequence complementary to the target analyte for detection.
The target analyte can be a DNA or an RNA sequence. A PNA probe sequence may also be of any length and will contain the base sequence complementary to the target analyte for detection. The target analyte can be a DNA or an RNA sequence as PNA binds to both. PNA binds DNA and RNA
more tightly than does DNA, therefore the challenge sequence should not be able to displace the already bound target sequence.
Some examples of target sequences are listed below.
Listeria monocytogenes; a 19 base pair oligonucleotide that is specific for a 36S rRNA sequence; detection in food industry (milks, cheeses etc.) See: R. F. Wang W. W. Cao and M.G. Johnson, App. Environ.
Microbiol., 1991, 3666 - 70.
A11 cholera toxin producing Strains of Vibrio cholerea c hybridise specifically with a 23 base pair oligonucleotide sequence (water detection, health). See: A C. Wright et al., J. Clin. Microbiol., 1992, 2302.
Specific oligonucleotide probes for detection of various strains of Chiamydia and Gonorrhoea (health industry). See: R. Rossau et al, u. Clin. Microbiol., 1990, 944 8; J. Gen. Microbiol, 1989, 135, 1735 45; Loeffelholz, M. J, J. Clin. Microbiol., 1992,2847 51.
An excellent summary of current technologies that use DNA probes is found In "DNA Probes", 2nd Ed.: G. H Keller & M. M. Manak, Stockton Press, 1993.
In order that the nature of the present invention may be more clearly understood preferred forms thereof will now be described with reference to the following non-limiting examples.
Example 1: Lateral Segregation of DNA
Detection of target polynucleotide sequences can be illustrated by the following example in which specific DNA gating is observed for a target DNA
concentration of 5 nM (1 pmole). The total lack of any response in the presence of a non-complementary probe sequence can be seen in the controls.
1st layer: 9.3nM Linker Gramicidin B
1.1M Membrane spanner Lipid D
27.5nM Membrane spanner Lipid C
37M dithio diglyconic acid 75M Linker Lipid A
2nd layer: l4mM (DPE-PC:GDPE=7:3) : Biotinylated Gramicidin E =
50,000:1 in ethanol Electrodes with freshly evaporated gold (1000A) on chrome adhesion layer (200A) on glass microscope slides) were dipped into an ethanolic solution of the first layer components for 1 hr at room temperature, rinsed with ethanol, then stored at 4~C under ethanol until used for impedance measurements. The slide was clamped into a block containing teflon coated wells which defined the area of the working electrode as approximately l6mmZ.
A11 steps were carried out at room temperature. 5~L of the 2nd layer was added to the working electrode before addition of a 180L volume of phosphate buffered saline (lOmM NaZHP04, 1mM KHZP04, 137mM NaCI, 2.7mM KCI, PBS). The electrode was washed 4 times using PBS.
Streptavidin was added to a11 wells (5~L 0.01mg/mL in PBS) and allowed to react with biotinylated Gramicidin E for 10-15 minutes before washing out excess unbound streptavidin with PBS. 5~L of a 1:1 mixture of DNA probe F
(200nM):DNA probe G (200nM in PBS) was added to sensor wells. A DNA
non-specific binding probe H (5~L 400 nM in PBS) was added to control wells. The probes were allowed to react with streptavidin for 10-15 minutes then excess unbound probes were washed out with PBS. 100~tL of DNA
target I (lOnM) in PBS was added to each well. The binding of DNA target I
to the sensor wells gave a decrease in the admittance at minimum phase, but no significant change in membrane admittance in control wells (Figure 1).
The amount and rate of decrease of admittance at minimum phase is related to the amount of DNA present in the test solution and therefore can be used to determine concentration in test solutions.
DNA probe F:
5'biotinylated listeria probe DNA with a 31-atom phosphoramidite linker group between the biotin and DNA.
5'-bio-L-M-ATAGTTTTATGGGATTAGC-3' DNA probe G:
5'biotinylated cholera toxin probe DNA with a 31-atom phosphoramidite linker group between the biotin and DNA.
5'-bio-L-M-CTCCGGAGCATAGAGCTTGGAGG-3' DNA non-specific binding probe H:
5'biotinylated 15-mer oligonucleotide with a 31-atom phosphoramidite linker group between the biotin and DNA, which is non-complementary to all parts of the target DNA sequence.
5'-bio-L-M-ATTGCTACGTATACG-3' DNA target I:
67 base DNA sequence containing the 19-base listeria sequence, a 10 base 'spacer' and the 23 base cholera toxin sequence.
5'-GCTAATCCCATAA.A.ACTATGCATGCATGCATCGTACGTACGTA
CCCTCCAAGCTCTATGCTCCGGAG-3' where:
bio = biotin L=
O
O-DMT
O-P-O
II
O
WO 97/44651 PCTlAU97/00316 M=
o~
-o~o~o~o'~o~~'~o-P=o 5 Example Z: Lateral Segregation of DNA followed by enzymatic cleavage This example illustrates the ability to perform a second, confirmatory step whereby an enzyme can be used to cleave the bound polynucleotide, thus confirming that a specific region of interest is present.
1st layer: 9.3nM Linker Gramicidin B
l.luM Membrane spanner Lipid D
27.5nM Membrane spanner Lipid C
37uM dithio diglyconic acid 75uM Linker Lipid A
2nd layer: l4mM (DPE-PC:GDPE=7:3) : Biotinylated Gramicidin E =
50,000:1 in ethanol Electrodes were prepared and 2nd layer added as described in Example 1.
Subsequent streptavidin, DNA probe and DNA target sequences were added as described in Example 1, except that they were carried out at 30~C.
After 15 minutesof DNA gating, unbound DNA target I was washed out with DNase I activation buffer. DNase I activation buffer consists of 50 nM
Tris.HCl, pH 7.6, 50 nM NaCI, 10 nM MgClZ, 10 nM MnClz, 0.2 mg/mL BSA.
DNase I was added (2 yL 1mg/mL in a 50%W~~ glycerol solution of 20 mM
Tris.HCl, pH 7.6, 1 mM MgClz) to sensor and control wells. Addition of DNase I gave an increase in admittance at minimum phase for sensor wells, but no significant increase for control wells (figure 2), showing that cleavage of DNA was being detected.
Example 3: DNA gating by addition of 2 biotinylated complementary polynucleotide sequences This example illustrates the possibility of detecting only one specific sequence on the polynucleotide of interest by having a capture molecule incorporated in the target. It also illustrates the use of peptide nucleic acid (PNA) sequences.
1st layer: 9.3nM Linker Gramicidin B
l.luM Membrane spanner Lipid D
5.5nM Membrane spanner Lipid C
37uM dithio diglyconic acid 75uM Linker Lipid A
2nd layer: l4mM (DPE-PC:GDPE=7:3) : Biotinylated Gramicidin E =
50,000:1 in ethanol Electrodes were prepared and 2nd layer added as described in Example 1. All steps were carried out at room temperature. 5~L of the 2nd layer was added to the working electrode before addition of a 180L volume of phosphate buffered saline (lOmM Na2HP0~, 1mM KHZP04, 137mM NaCI, 2.7mM KCl, PBS). The electrode was washed 4 times using PBS.
Streptavidin was added to all wells (5~L 0.01mg/mL in PBS) and allowed to react with biotinylated Gramicidin E for 10-15 minutes before washing out excess unbound streptavidin with PBS.
5 nM of each of PNA sequence J and the complementary DNA
sequence K (1.14,L 1.75 ~M) were added quickly in succession to the sensor wells. No PNA or DNA sequence was added to the control wells. The binding of the PNA (J) and DNA (K) sequences to the streptavidin and each other gave a decrease in the admittance at minimum phase, but no significant change in membrane admittance in control wells (Figure 3). The amount and rate of decrease of admittance at minimum phase is related to the amount of DNA or PNA present in the test solution and therefore can be used to determine concentration in test solutions.
PNA sequence J:
N-biotinylated listeria probe sequence PNA containing glycine and lysine for solubility plus an 8-amino-3,6-dioxaoctanoic acid linker.
N-bio-gly-lys-O-ATAGTTTTATGGGATTAGC-CONHz DNA sequence K:
5'-biotinylated listeria DNA with no linker group between the biotin and DNA.
5'-bio-GCTAATCCCATAAAACTAT-3' where O=
o H
N.
~~O
It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in ZO the specific embodiments without departing from the spirit or scope of the invention as broadly described. These include the detection of PCR (or other amplification method) products and the detection of genetic mutations in genetically derived diseases, where the mutation is known. A list of some 3500 conditions due to defective genes can be found in McKusick's "Mendelian Inheritance in Man" and further examples are regularly reported in the scientific press. The present embodiments are, therefore, to be considered in a11 respects as illustrative and not restrictive.
17a SEQUENCE LISTING
(1) GENERAL INFORMATION:
(i) APPLICANT:
(A) NAME: Australian Membrane and Biotechnology Research Institute (B) STREET: 126 Greville St (C) CITY: Chatswood (D) STATE: New South Wales (E) COUNTRY: Australia (F) POSTAL CODE (ZIP): 2067 (A) NAME: The University of Sydney (C) CITY: Sydney (D) STATE: New South Wales (E) COUNTRY: Australia (F) POSTAL CODE (ZIP): 2006 (ii) TITLE OF INVENTION: Nucleic acid sensor (iii) NUMBER OF SEQUENCES: 6 (iv) CORRESPONDENCE ADDRESS:
(A) ADDRESSEE: SWABEY OGILVY RENAULT
(B) STREET: Suite 1600, l981 McGill College Avenue (C) CITY: Montreal (D) STATE: QC
(E) COUNTRY: Canada (F) ZIP: H3A 2Y3 (v) COMPUTER READABLE FORM:
(A) MEDIUM TYPE: Floppy disk (B) COMPUTER: IBM PC compatible (C) OPERATING SYSTEM: PC-DOS/MS-DOS
(D) SOFTWARE: PatentIn Release #1.0, Version #1.30 (EPO) (vi) CURRENT APPLICATION DATA:
(A) APPLICATION NUMBER: 2,255,952 (B) FILING DATE: 22-MAY-1997 (C) CLASSIFICATION:
(vi) PRIOR APPLICATION DATA:
(A) APPLICATION NUMBER: PCT/AU97/00316 (B) FILING DATE: 22-MAY-1997 (vi) PRIOR APPLICATION DATA:
(A) APPLICATION NUMBER: 60/018,125 (B) FILING DATE: 22-MAY-1996 (viii) ATTORNEY/AGENT INFORMATION:
(A) NAME: Cote, France (B) REGISTRATION NUMBER: 4166 (C) REFERENCE/DOCKET NUMBER: 3650-97 FC/ntb (ix) TELECOMMUNICATION INFORMATION:
(A) TELEPHONE: 514-845-7126 (B) TELEFAX: 514-288-B389 17b (C) TELEX:
(2) INFORMATION FOR SEQ ID NO: 1:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 19 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID N0: 1:
atagttttat gggattagc 19 (2) INFORMATION FOR SEQ ID NO: 2:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 23 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 2:
ctccggagca tagagcttgg agg 23 (2) INFORMATION FOR SEQ ID NO: 3:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 15 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 3:
attgctacgt atacg 15 (2) INFORMATION FOR SEQ ID NO: 4:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 67 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide 17c (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 4:
gctaatccca taaaactatg catgcatgca tcgtacgtac gtaccctcca agctctatgc 60 tccggag 67 (2) INFORMATION FOR SEQ ID N0: 5:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 19 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 5:
atagttttat gggattagc 19 (2) INFORMATION FOR SEQ ID NO: 6:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 19 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 6:
gctaatccca taaaactat 19
Claims (25)
1. A biosensor for use in detecting the presence of a selected nucleic add sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand reactive with the selected nucleic acid or marker attached thereto is attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane.
2. A biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning spanning monomers proximal the surface of the membrane and a second ligand attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane, the second ligand having bound thereto or included therein the selected nucleic acid sequence such that the first ligands binds to the second ligand.
3. A biosensor as claimed in claim 1 or claim 2 in which the membrane includes membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane.
4. A biosensor for use in detecting the presence of a selected nucleic add sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleicacid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand reactive with the selected nucleic acid or marker attached thereto attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or the end of the membrane-spanning amphiphiles proximal the surface of the membrane.
5. A biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleicacid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or the end of the membrane-spanning amphiphiles proximal the surface of the membrane, the second ligand having bound thereto or included therein the selected nucleic acid sequence such that the first ligands binds to the second ligand.
6. A biosensor as claimed in any one of claims 1 to 5 in which the first ligand comprises a nucleic acid molecule or PNA which includes a sequence complementary to a first sequence within the selected nucleic acid.
7. A biosensor as claimed in any one of claims 1 to 6 in which the second ligand is an antibody directed against DNA, or binding fragment thereof.
8. A biosensor as claimed in any one of claims 1 to 6 in which the second ligand is an intercalating agent, major or minor groove binder, an agent capable of triple helix formation or an agent which can covalently couple to DNA.
9. A biosensor as claimed in any one of claims 1 to 6 in which the second ligand is specific for the selected nucleic acid sequence
10. A biosensor as claimed in any one of claims 1 to 9 in which the first and second ligands are attached via linkers to the ion channels or membrane spanning lipids.
11. A biosensor as claimed in claim 10 in which the linker is a phosphoramidite linker group.
12. A biosensor for use in detecting the presence of a selected nucleic acid sequence in a sample, the biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence of the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer and a first ligand specifically reactive with the selected nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane.
13. A biosensor as claimed in claim 12 in which the first ligand comprises a nucleic acid molecule or PNA which includes a sequence complementary to a first sequence within the selected nucleic acid.
14. A biosensor as claimed in claim 12 or 13 in which the first ligand is attached via linkers to the ion channels.
15. A biosensor as claimed in claim 14 in which the linker is a phosphoramidite linker group.
16. A biosensor as claimed in any one of claims 1 to 15 in which the first and second half membrane spanning monomers are gramicidin or one of its derivatives.
17. A method of detecting the presence of a selected nucleic acid within a sample, the method comprising the following steps:
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with a first nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane, either the first or second nucleic acid sequence being within the sequence of a selected nucleic acid;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with a first nucleic acid sequence attached to an end of a proportion of the first half membrane-spanning monomers proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to an end of the remainder of the first half membrane-spanning monomers proximal the surface of the membrane, either the first or second nucleic acid sequence being within the sequence of a selected nucleic acid;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
18. A method of detecting the presence of a selected nucleic acid sequence within a sample, the method comprising the following steps:
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or an end of the membrane-spanning amphiphiles proximal the surface of the membrane;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
(i) providing a biosensor comprising an electrode and a bilayer membrane having a top and a bottom layer, the bottom layer being proximal to and connected to the electrode in a manner such that a space exists between the membrane and the electrode, the conductance or impedance of the membrane being dependent on the presence or absence or the selected nucleic acid sequence, the membrane comprising a closely packed array of amphiphilic molecules, membrane spanning amphiphiles which are prevented from lateral diffusion within the membrane and a plurality of ion channels comprising first half membrane spanning monomers dispersed in the top layer and second half membrane spanning monomers dispersed in the bottom layer, the first half membrane spanning monomers being capable of lateral diffusion within the upper layer and the second half membrane-spanning monomers being prevented from lateral diffusion within the bottom layer, a first ligand specifically reactive with the selected nucleic acid sequence attached to either an end of at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or to an end of the membrane-spanning amphiphiles proximal the surface of the membrane and a second ligand specifically reactive with a second nucleic acid sequence attached to the other of the at least a proportion of the first half membrane-spanning monomers proximal the surface of the membrane or an end of the membrane-spanning amphiphiles proximal the surface of the membrane;
(ii) adding a sample suspected to contain the selected nucleic acid to the biosensor and measuring the conductance and/or impedance of the membrane; and (iii-) adding a challenge nucleic acid to the biosensor from (ii) and measuring the conductance and/or impedance of the membrane, the challenge sequence being selected such that it includes both the first and second nucleic acid sequences.
19. A method as claimed in claims 17 or 18 in which the first ligand comprises a nucleic acid molecule or PNA which includes a sequence complementary to a first sequence within the selected nucleic acid.
20. A method as claimed in any one of claims 17 to 19 in which the second ligand is an antibody directed against DNA, or binding fragment thereof.
21. A method as claimed in any one of claims 17 to 19 in which the second ligand is an intercalating agent, major or minor groove binder, an agent capable of triple helix formation or an agent which can covalently couple to DNA.
22. A method as claimed in any one of claims 17 to 19 in which the second ligand is specific for the selected nucleic acid sequence
23. A method as claimed in any one of claims 17 to 23 in which the first and second ligands are attached via linkers to the ion channels or membrane spanning lipids.
24. A method as claimed in claim 23 in which the linker is a phosphoramidite linker group.
25. A method as claimed in any one of claims 17 to 24 in which the first and second half membrane spanning monomers are gramicidin or one of its derivatives.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1812596P | 1996-05-22 | 1996-05-22 | |
| US60/018,125 | 1996-05-22 | ||
| PCT/AU1997/000316 WO1997044651A1 (en) | 1996-05-22 | 1997-05-22 | Nucleic acid sensor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2255952A1 true CA2255952A1 (en) | 1997-11-27 |
Family
ID=21786371
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002255952A Abandoned CA2255952A1 (en) | 1996-05-22 | 1997-05-22 | Nucleic acid sensor |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0990149A4 (en) |
| JP (1) | JP2000513811A (en) |
| AU (1) | AU734086B2 (en) |
| CA (1) | CA2255952A1 (en) |
| WO (1) | WO1997044651A1 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5952172A (en) | 1993-12-10 | 1999-09-14 | California Institute Of Technology | Nucleic acid mediated electron transfer |
| US5591578A (en) * | 1993-12-10 | 1997-01-07 | California Institute Of Technology | Nucleic acid mediated electron transfer |
| US6071699A (en) | 1996-06-07 | 2000-06-06 | California Institute Of Technology | Nucleic acid mediated electron transfer |
| US5824473A (en) | 1993-12-10 | 1998-10-20 | California Institute Of Technology | Nucleic acid mediated electron transfer |
| AUPN366895A0 (en) * | 1995-06-20 | 1995-07-13 | Australian Membrane And Biotechnology Research Institute | Detection of small analytes |
| US6387625B1 (en) | 1995-06-27 | 2002-05-14 | The University Of North Carolina At Chapel Hill | Monolayer and electrode for detecting a label-bearing target and method of use thereof |
| US6127127A (en) * | 1995-06-27 | 2000-10-03 | The University Of North Carolina At Chapel Hill | Monolayer and electrode for detecting a label-bearing target and method of use thereof |
| US6444423B1 (en) | 1996-06-07 | 2002-09-03 | Molecular Dynamics, Inc. | Nucleosides comprising polydentate ligands |
| US7160678B1 (en) | 1996-11-05 | 2007-01-09 | Clinical Micro Sensors, Inc. | Compositions for the electronic detection of analytes utilizing monolayers |
| US7045285B1 (en) | 1996-11-05 | 2006-05-16 | Clinical Micro Sensors, Inc. | Electronic transfer moieties attached to peptide nucleic acids |
| US7014992B1 (en) * | 1996-11-05 | 2006-03-21 | Clinical Micro Sensors, Inc. | Conductive oligomers attached to electrodes and nucleoside analogs |
| US6096273A (en) | 1996-11-05 | 2000-08-01 | Clinical Micro Sensors | Electrodes linked via conductive oligomers to nucleic acids |
| US7381525B1 (en) | 1997-03-07 | 2008-06-03 | Clinical Micro Sensors, Inc. | AC/DC voltage apparatus for detection of nucleic acids |
| US7393645B2 (en) | 1996-11-05 | 2008-07-01 | Clinical Micro Sensors, Inc. | Compositions for the electronic detection of analytes utilizing monolayers |
| US6503452B1 (en) * | 1996-11-29 | 2003-01-07 | The Board Of Trustees Of The Leland Stanford Junior University | Biosensor arrays and methods |
| US6306584B1 (en) * | 1997-01-21 | 2001-10-23 | President And Fellows Of Harvard College | Electronic-property probing of biological molecules at surfaces |
| US6013459A (en) | 1997-06-12 | 2000-01-11 | Clinical Micro Sensors, Inc. | Detection of analytes using reorganization energy |
| US7560237B2 (en) | 1997-06-12 | 2009-07-14 | Osmetech Technology Inc. | Electronics method for the detection of analytes |
| IL121312A (en) | 1997-07-14 | 2001-09-13 | Technion Res & Dev Foundation | Microelectronic components, their fabrication and electronic networks comprising them |
| US6686150B1 (en) | 1998-01-27 | 2004-02-03 | Clinical Micro Sensors, Inc. | Amplification of nucleic acids with electronic detection |
| US6761816B1 (en) | 1998-06-23 | 2004-07-13 | Clinical Micro Systems, Inc. | Printed circuit boards with monolayers and capture ligands |
| US6740518B1 (en) | 1998-09-17 | 2004-05-25 | Clinical Micro Sensors, Inc. | Signal detection techniques for the detection of analytes |
| IL126776A (en) | 1998-10-27 | 2001-04-30 | Technion Res & Dev Foundation | Method for gold depositions |
| WO2000024941A1 (en) | 1998-10-27 | 2000-05-04 | Clinical Micro Sensors, Inc. | Detection of target analytes using particles and electrodes |
| US6833267B1 (en) | 1998-12-30 | 2004-12-21 | Clinical Micro Sensors, Inc. | Tissue collection devices containing biosensors |
| US6942771B1 (en) | 1999-04-21 | 2005-09-13 | Clinical Micro Sensors, Inc. | Microfluidic systems in the electrochemical detection of target analytes |
| US7364920B2 (en) | 1999-10-27 | 2008-04-29 | Technion Research And Development Foundation Ltd. | Method for gold deposition |
| DE10015547C2 (en) * | 2000-03-30 | 2002-02-14 | Aventis Res & Tech Gmbh & Co | Method for the detection of molecules by means of impedance spectroscopy and device for carrying out these methods |
| CA2408351A1 (en) * | 2000-05-18 | 2001-11-22 | The Board Of Trustees Of The Leland Stanford Junior University | Lipid bilayer array methods and devices |
| WO2005016115A2 (en) | 2003-01-23 | 2005-02-24 | Montana State University | Biosensors utilizing dendrimer-immobilized ligands and their use thereof |
| US7824927B2 (en) * | 2005-04-05 | 2010-11-02 | George Mason Intellectual Properties, Inc. | Analyte detection using an active assay |
| US8906609B1 (en) | 2005-09-26 | 2014-12-09 | Arrowhead Center, Inc. | Label-free biomolecule sensor based on surface charge modulated ionic conductance |
| CA3002886A1 (en) * | 2015-10-21 | 2017-04-27 | F. Hoffmann-La Roche Ag | Use of fluoropolymers as a hydrophobic layer to support lipid bilayer formation for nanopore based dna sequencing |
| CN113070113B (en) * | 2021-06-03 | 2021-08-20 | 成都齐碳科技有限公司 | Chip structure, film forming method, nanopore sequencing device and application |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0455705B1 (en) * | 1989-01-27 | 1997-05-28 | Australian Membrane And Biotechnology Research Institute | Receptor membranes and ionophore gating |
| US5328847A (en) * | 1990-02-20 | 1994-07-12 | Case George D | Thin membrane sensor with biochemical switch |
| DE69232641T2 (en) * | 1991-03-27 | 2003-02-20 | Ambri Ltd | IONIC RESERVOIR ON THE SURFACE OF AN ELECTRODE |
| AU681138B2 (en) * | 1993-04-21 | 1997-08-21 | Ambri Limited | Surface amplifier |
| AUPM950094A0 (en) * | 1994-11-16 | 1994-12-08 | Australian Membrane And Biotechnology Research Institute | Detection device and method |
| AUPN366995A0 (en) * | 1995-06-20 | 1995-07-13 | Australian Membrane And Biotechnology Research Institute | Self-assembly of bilayer membrane sensors |
-
1997
- 1997-05-22 WO PCT/AU1997/000316 patent/WO1997044651A1/en not_active Application Discontinuation
- 1997-05-22 EP EP97921532A patent/EP0990149A4/en not_active Withdrawn
- 1997-05-22 CA CA002255952A patent/CA2255952A1/en not_active Abandoned
- 1997-05-22 JP JP09541274A patent/JP2000513811A/en active Pending
- 1997-05-22 AU AU27578/97A patent/AU734086B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP2000513811A (en) | 2000-10-17 |
| WO1997044651A1 (en) | 1997-11-27 |
| AU2757897A (en) | 1997-12-09 |
| AU734086B2 (en) | 2001-05-31 |
| EP0990149A4 (en) | 2003-02-26 |
| EP0990149A1 (en) | 2000-04-05 |
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|---|---|---|---|
| FZDE | Dead |