The present invention relates to a sensor, and more particularly to a biosensor, for use as a tool in molecular biological analysis.
The term “biosensor” is understood to mean a functional assembly, for one-time use or not, for example use for the purpose of a molecular biological determination, designed and/or intended to cooperate with at least one separate and complementary apparatus or instrument that receives a liquid or fluid, immobile or moving, specimen of interest, said liquid specimen comprising at least one target species, in suspension or in solution, for example an optionally labeled biomolecule; and the biosensor delivers at least one output signal relating to the presence and/or the nature and/or the structure and/or the quantity of said target species. As regards a small biosensor, for example of the order of one centimeter, this may be called a “biochip” according to the terminology adopted in the technical field in question.
The biosensor comprises at least:
The dimensions of these biosensors, for example, from around 1 mm2 to a few cm2, may require the use of “micro” techniques or “nanotechnologies”, for example lithography or micromachining, in order to produce them.
However, the Applicant does not intend to be limited to particular dimensions, for example of the order of 1 μm or 1 nm, when the term “sensor”, “biosensor” or “biochip” is used in the present description and in the appended claims, considering that the same structure or the same arrangement as that defined below may be used with dimensions of the order of a few mm2, just as with much larger dimensions.
Of course, a biosensor as considered by the present invention does not operate autonomously, unless its own power supply is incorporated with it. Consequently, this biosensor is designed to cooperate, for example, in a removable manner, on the one hand with external means for making the liquid specimen of interest, but also other fluids or liquids such as a washing liquid, circulate or remain in contact with the operating surface and with the ligands, and on the other hand with means for detecting and for processing the output signal or signals, all this being in general monitored and controlled by external, analog or computer, electronic means, for example, according to any processing flowchart or software.
The term “biomolecule” is understood to mean any entity, in particular a biochemical or biological entity, identical to or derived from any molecular species existing in nature. Among the biomolecules considered by the present invention, mention may be made of certain biopolymers, for example DNA and RNA, oligonucleotides and polynucleotides, functional or structural proteins, peptides, oligopeptides and polypeptides, polysaccharides, etc.
The term “labeling” or “labeled” is understood to mean the characteristic whereby a label is attached to an entity, for example the target species, in a covalent or other manner, said label being a substituent or residue for producing a signal, referred to above as the output signal, with or without the aid of an external means, such as illumination, and with or without a subsequent step, such as one of contacting it with a substrate.
The preferred labels according to the present invention are:
The term “determination” is understood to mean the qualitative and/or quantitative identification, the detection, the description (for example sequencing), the separation or the enrichment of the target species, which may be called the “analyte” in the case of a qualitative and/or quantitative identification. According to the present invention, the term “determination” includes any sequencing of a biomolecule of the DNA or polypeptide type.
The output signal or signals for the purposes of determination may be of any appropriate type, depending on the labels used, and on the type of detection required. They may be visible or invisible light signals, electrical signals, electrooptic signals, electrochemical signals, etc. Moreover, these signals may where appropriate be detected separately, taking into account, on the one hand, the addressing of the biosensor electrodes and, on the other hand, the set of connections of the electrical terminals to the various respective electrodes present on the biosensor.
The term “ligand” is understood to mean any cellular or biological entity, or biomolecule, having a specific or nonspecific affinity for a target species. Affinity means that it forms, under the conditions (especially temperature, pH, ionic force, etc.) in which the target species is brought into contact with the ligand, a stable complex or pairing between said target species and said ligand. As an example of a ligand, mention may be made of any oligonucleotide capable of binding via weak bonds—in this case we speak of hybridization with a DNA strand (target species) having a sequence complementary to that of the ligand.
Each ligand is attached or anchored at each site or on each electrode of the biosensor, possibly after functionalization of the elementary sites of the operating surface of the support by any suitable means, for example chemical means, by covalent bonding, for example via a spacer arm, or by adsorption, absorption, etc.
With regard to the elementary sites coated, as indicated above, with a polymer of the polythiophene or modified polypyrrole type and electrically addressed, the ligands may be fixed using the electrochemical techniques described in documents FR 2 789 401, EP 1 152 821, WO 00/47317, FR 2 742 451, EP 0 868 464 and WO 97/22648.
The term “target species” is understood to mean any biological or biochemical cell species capable of being bonded via a weak bond to one or more ligands.
With regard to a biosensor of the biochip type, in the current state of the art in the technical sector in question, a distinction may be made between two routes of obtaining respectively different ligands, each multiply attached to the various electrodes respectively:
At the present time, biosensors of the biochip type are simple or complex tools that are well suited to all kinds of analysis in molecular biology, see “DNA chips: a new tool for genetic analysis and diagnostics” by M. Cuzin, Transfusion Clinique et Biologique 2001; 8:291-6; and “How to make a DNA chip” by Michael C. Pirrung, Angew. Chem. Int. Ed 2002.41, 1276, 1289.
In general, a biosensor as described above is placed at the bottom of a well, a microtitration plate, within which the liquid specimen comprising the target species is introduced, resides and from which it is then removed.
The subject of the present invention is a sensor, in particular a biosensor, for example a biochip, which is particularly simple to manufacture or produce and can be used in the most varied of ways, for example in the wells of a microplate.
According to the present invention on the one hand the multiplicity of electrodes is placed in an extreme zone on the opposite side from another extreme zone in which the electrical terminals are grouped together, and on the other hand the support includes at least one flexible zone located between the two extreme zones.
Preferably, the entire support is flexible and produced, for example, from a thin, flexible insulating material.
The term “flexible” is understood to mean in particular that the zone of the same name can bend about at least one axis having a direction perpendicular to the direction of alignment of the operating arrangement of the electrodes and of the group of electrical terminals.
Preferably, the support is a flexible sheet or plate made of insulating material.
Thanks to the present invention, the purely electrical zone of the sensor is shifted relative to its active zone, that is to say that zone having the electrodes and grouping them together, to which the ligands are respectively attached, and this is done by allowing any relative position between the two extreme zones having the electrical terminals and the electrodes respectively, thanks to the flexibility of the support, at least in its intermediate zone between the two said extreme zones.
Thus, the electrodes may be immersed in a liquid solution, whereas the electrical terminals are in the open air and/or in the dry. This makes it possible to achieve, under excellent technical or practical conditions:
A sensor according to the invention makes it possible to fabricate and employ biochips in a completely different approach from the conventional approach, by:
The present invention will now be described with reference to the appended drawing, in which:
According to
According to the invention, in combination, on the one hand the multiplicity of electrodes (4) is placed in a zone (1a) on the opposite side from a zone (1b) in which the multiplicity of electrical terminals (5) are grouped together and, on the other hand, the support (2) owing to the flexibility of the insulating material employed, is designed to be flexible at least in an intermediate zone (1c), at least about at least one axis having a direction perpendicular to the direction of alignment of the operating arrangement of the electrodes (31 and 32) in the zone (1a) and of the group of electrical terminals (5) in the zone (1b).
Each assembly, composed of an electrode (31) and an electrode (32), may be seen as one and the same electrode having two adjacent ends connected together.
According to the embodiment shown in
Of course, the arrangement described above could be applied on the useful face (2a).
According to the embodiment shown in
The track (7) and/or the track (10) thus described may be assigned to the electrical shielding of the arrangement of the electrodes (31 and 32) so as to prevent any electromagnetic radiation from interfering with the address or measurement signals.
As shown in
With regard to a biosensor, of the biochip type, a plurality of ligands are each multiply attached to the respectively different electrodes (31 and/or (32).
A sensor, or “flexichip” according to the invention is employed, before or after addressing, or before or after hybridizing, as shown schematically in
A flexichip according to the invention is addressed as follows:
The nucleotide sequences of the probes deposited are, for example:
Number | Date | Country | Kind |
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0209232 | Jul 2002 | FR | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/FR03/02287 | 7/18/2003 | WO | 1/11/2005 |