Biosensors have been constructed comprising biomembranes which are a double layer of closely packed amphiphilic lipid molecules. The molecules of these bilayers exhibit the random motions characteristic of the liquid phase, in which the hydrogen tails of the lipid molecules have sufficient mobility to provide a soft, flexible, viscid surface. The molecules can also diffuse sideways freely within their own monolayer so that two neighbouring lipids in the same monolayer exchange places with each other about once every microsecond, while the lipid molecules in opposite monolayers exchange places on the average of one a year.

These membranes may incorporate a class of molecules, called ionophores, which facilitate the transport of ions across these membranes.

Ion channels are a particular form of ionophore, which as the term implies, are channels through which ions may pass through membranes. A favoured ionophore is gramicidin A which forms aqueous channels in the membrane.

Examples of such biosensors are disclosed in the following International Patent Applications, the disclosures of which are incorporated herein by cross reference: PCT/AU88/00273, PCT/AU89/00352, PCT/AU90/00025, PCT/AU92/00132, PCT/AU93/00509, PCT/AU93/00620, PCT/AU94/00202, PCT/AU95/00763, PCT/AU96/00304, PCT/AU96/00368, PCT/AU96/00369 and PCT/AU96/00482.

The first of these references discloses receptor molecules conjugated with a support that is remote from the receptor site. The support may be a lipid head group, a hydrocarbon chain, a cross-linkable molecule or a membrane protein.

The inner level of the membrane may be adjacent a solid surface with groups reactive with the solid surface, and spaced from the surface to provide a reservoir region as disclosed in U.S. Patent No. 5,401,378.

Biosensors based on ion channels or ionophores contained within lipid membranes tethered to or deposited onto metal electrodes are disclosed in Australian Patent 623,747 and U.S. patent 5,234,566. Those references

disclose a membrane bilayer in which each layer has incorporated therein ionophores and in which the conductance of the membrane is dependent upon the presence or absence of an analyte. The disclosure of Australian Patent 623,747 (incorporated herein by reference) describes various ionophore gating mechanisms termed local disruption gating, extended disruption gating, vertical disruption gating, and extended displacement gating mechanisms to modify the conductivity of the membrane in response to the presence of an analyte. In each of those gating mechanisms an inner layer of the membrane (the layer closer to the solid electrode surface, if any) contains immobilised or tethered half membrane spanning ion channels which an outer layer contains more mobile half membrane spanning ion channels. One method for immobilising the ion channels of the inner layer is to employ a polymerisable lipid layer and then cross-link the molecules of the inner monolayer and the ionophore. The conductivity of the membrane is altered by the extent to which opposing half membrane spanning ion channels align to establish a membrane spanning channel for ion transmission across the membrane.

In local disruption gating receptor molecules are linked to mobile ionophores in the outer layer that are aligned with tethered or immobilised ionophores in the inner layer. The introduction of an analyte particle that binds to two adjacent receptors in the outer layer causes the disruption of the orderly alignment of the membrane spanning ionophore. In the case of local disruption gating a loss of conductivity occurs due to the deformation of the ionophores of the outer layer caused by the bonding of the analyte with the adjacent receptors.

The mechanism of extended disruption gating is similar, except that the displacement of the mobile ionophore is greater. In extended disruption gating the binding of pairs of receptors to the same analyte particle cause the outer layer ionophores to move completely out of alignment with the inner layer ionophores.

The mechanism of vertical disruption gating is also similar. In that case the presence of the analyte particle bound to two receptor molecules causes a separation of the two layers that disrupts the continuity of the ion channel across the membrane.

The mechanism of extended displacement gating utilises two different receptors that bind to each other and are linked receptively to a half

membrane ionophore and a membrane molecule. The binding of these two receptor molecules to each other displaces the ionophore and disrupts conductivity. The analyte competes with the second receptor for the binding site on the first receptor. The presence of the analyte breaks the bond between the two receptors and allows the half membrane ionophores to realign and provide an ion conductive path. Each of these mechanisms has in common that the binding of the analyte to the receptor molecule causes a change in the relationship between two half membrane spanning monomers such that the flow of ions across the membrane via the ionophores is allowed or prevented.

In a number of sensing applications it is beneficial to incorporate within the one detection cell a positive or negative control to add to the utility of the biosensor. As will be recognised the fabrication of a biosensor having discrete areas of membrane which act as either a test area or control area can be very complex. The present inventors have developed methods by which such biosensors may be fabricated in a less complex manner using optically sensitive moieties.

In a number of sensing applications it is beneficial to incorporate within the one detection cell a positive or negative control to add to the utility of the biosensor. As will be recognised the fabrication of a biosensor having discrete areas of membrane which act as either a test area or control area can be very complex. The present inventors have developed methods by which such biosensors may be fabricated in a less complex manner using optically sensitive moieties.

Accordingly in a first aspect the present invention consists in a method of fabricating a biosensor in which there is at least one discrete test and at least one discrete control zone, the method comprising the following steps: (i) providing a conductive substrate; (ii) forming a membrane including membrane spanning lipids and ion channels comprising first and second half membrane spanning monomers such that the membrane is tethered to the conductive substrate such that a functioning reservoir exists between the membrane and the conductive substrate; (iii) linking a ligand reactive with an analyte of interest to the ion-channel and linking a ligand reactive with an analyte of interest to the

membrane spanning lipid components of the tethered membrane via photocleavable linkers; and (iv) exposing the membrane to a focused light source to cleave the photocleavable linkers thereby releasing the ligands from the ion- channel and membrane spanning lipid components in discrete areas of the membrane.

In a preferred embodiment the method further includes the following step: (v) binding control ligands to the ion channels and membrane spanning lipid components after the ligands have been removed in step (iv).

In a further preferred embodiment the membrane is rinsed between steps (iv) and (v).

In a second aspect the present invention consists in a method of fabricating a biosensor in which there is at least one discrete test and at least one discrete control zone, the method comprising the following steps: (i) providing a conductive substrate; (ii) forming a membrane including membrane spanning lipids and ion channels comprising first and second half membrane spanning monomers such that the membrane is tethered to the conductive substrate such that a functioning reservoir exists between the membrane and the conductive substrate; (iii) providing on the ion channels and membrane spanning lipids a photoactivatable group which when illuminated will bind a receptor; (iv) illuminating discrete areas of the membrane and linking a ligand reactive with an analyte of interest to the ion-channel and membrane spanning lipid components of the tethered membrane via photoactivatable group to form test areas; (v) removing unbound ligand; and (vi) linking a control ligand to the remainder of the ion-channels and membrane spanning lipid components of the tethered membrane to form control areas.

The photocleavable linkers may be any of a number of such molecules known in the art (eg see Pillai (1980)). The photoactivatable groups may be any number of such groups known in the art, such as, for example, photoactivatable biotins described by Pirrung (1996) or Cass (1996).

The conductive substrate may, of course, be any of a range of such substrates known in the art, for example gold coated glass or silicon.

One advantage of this approach is the ability to fabricate differential electrodes (active versus control) with the high degree of spatial resolution achievable using optical methods, and unachievable using other methods (such as controlled liquid deposition). This high degree of spatial resolution would result in improved common mode rejection and therefore improved sensitivity as well as simplifying the manufacturing process.

In a third aspect the present invention consists in an improved biosensor, the biosensor comprising a membrane and an electrode having a conductive substrate, the membrane including membrane spanning lipids and ion channels comprising first and second half membrane spanning monomers, the membrane being attached to the conductive substrate such that a functioning reservoir exists between the membrane and the conductive substrate, ligands specific for an analyte attached the ion channels and membrane spanning lipids, the improvement comprising providing on at least one of the first and second half membrane spanning monomers a photocleavable/switchable group which inhibits dimer formation.

In a fourth aspect the present invention consists in an improved biosensor, the biosensor comprising a membrane the conductance/impedance of which is altered by the presence or absence of an analyte and a conductive substrate, the membrane including membrane spanning lipids and ion channels comprising first and second half membrane spanning monomers such that the membrane is tethered to the conductive substrate such that a functioning reservoir exists between the membrane and the conductive substrate, and ligands attached to the ion channels and membrane spanning lipids. the improvement comprising providing on at least one of the first and second half membrane spanning monomers or membrane spanning lipids a photoswitchable group derived from a compound in accordance with Formula 1.

Formula 1 wherein R1 represents 0 to about 3 groups where each is independently H or saturated or unsaturated, substituted or unsubstituted Ci l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14 hydrocarbon; R2 represents 0 to about 3 groups where each is independently hydrogen or saturated or unsaturated, substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted ClA hydrocarbon; Y represents H, saturated or unsaturated, substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted CIA hydrocarbon COR6, CONR7R8, COOR14, S(O)nRl5 where n is 0, 1 or 2, R6 R7, R8, Rl4 and R15 are each independently represent H, saturated or unsaturated, substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted ClA hydrocarbon or aryl; Rg is -C(O)X where X

represents H, saturated or unsaturated, substituted or unsubstituted Cl l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14 hydrocarbon, or OH, or OR10 in which Rlo is alkyl, or NRllRl2 in which R11 and Rl2 are H, alkyl or taken together with N form a ring, or aryl or Rg together with R1 form a substituted or unsubstituted 5-6 member cyclic or heterocyclic ring; Z represents 0 or NR13 R13 is H, saturated or unsaturated substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14 hydrocarbon or aryl.

The compound will include a functional group at Y or Rg such that the compound can be linked to at least one of the first and second half membrane spanning monomers or membrane spanning lipids.

Particularly preferred compounds from which the photoswitchable linkers are derived are shown in Formula 2 below.

Formula 2 wherein R1 represents 0 to about 3 groups where each is independently hydrogen or saturated or unsaturated, substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14 hydrocarbon; R2 represents 0 to about 3 groups where each is independently hydrogen or saturated or unsaturated, substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14 hydrocarbon; X represents H, saturated or unsaturated, substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14

hydrocarbon, or aryl, or OH, or OR10 in which R10 is alkyl, or NR1lRl2 in which R1l and R12 are H, alkyl or taken together with N form a ring,; Y represents H, or saturated or unsaturated, substituted or unsubstituted Cl l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14 hydrocarbon, COR6, CONR7R8, COOR14, S(O)nR15 where n is 0, 1 or 2, Re, R7, R6, R14 and R15 are each independently represent H, saturated or unsaturated, substituted or unsubstituted C1 l0 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C14 hydrocarbon or aryl; Z represents 0 or NR13 R13 is H, saturated or unsaturated, substituted or unsubstituted C1.10 hydrocarbon, preferably saturated or unsaturated, substituted or unsubstituted C1.4 hydrocarbon or aryl.

Specific examples of suitable photoswitchable linkers that are suitable for use in the present invention are shown in Figure 10.

It will be appreciated that certain compounds of Formula 1 are novel and the present invention therefore provides, in a fifth aspect, compounds in accordance with Formula 1, provided that when RO is -C(O)X and X is H, at least one of R1, R2, R3 or Y is other than H.

Throughout this specification, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.

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 and Figures in which:- Figures 1 to 9 are schematic representations of the biosensors of the presnt invention; and Figure 10 shows the structure of some of the compounds of the present invention.

An example of an improved biosensor in accordance with the invention is shown schematically in Figure 1.

The improved biosensor can be advantageously used in the detection of an analyte. An exemplary protocol for use of this type of biosensor is as follows.

An initial measurement of biosensor impedance is made and the sample suspected to contain the analyte is then added. A second measurement is made and a light source is triggered on. A third measurement of the time course response to light is made. The light source is then triggered off and a fourth measurement of the time course response to the removal of light is made. These later steps may be repeated, switching the light on and off.

Various combinations and subsets of the later measurement steps can be used depending on the type of photogroup and the level of sensitivity required. Such a construct would not allow a real gating response until illumination, and would therefore allow for non-specific effects (e.g. caused by serum addition) to be separately determined, and removed from the real gating response.

The benefits of another fabrication protocol is shown in Figure 2.

Accordingly, in a fifth aspect the present invention consists in a method comprising the following steps: (i) providing a conductive substrate; (ii) forming a membrane including membrane spanning lipids and ion channels comprising first and second half membrane spanning monomers, the membrane being attached to the conductive substrate such that a functioning reservoir exists between the membrane and the conductive substrate; (iii) providing on the half membrane spanning monomer remote from the conductive substrate a photoswitchable binder to streptavidin and providing biotin on the membrane spanning lipid; (iv) adding streptavidin; (v) triggering a light source and rinsing; (vi) triggering the light source off and adding streptavidin; (vii) optionally repeating steps (v) and (vi); and (viii) adding ligands specfic to an analyte to the ion channels and membrane spanning lipids.

It is preferred that the photoswitchable binder to streptavidin is caged biotin, HABA or derivative thereof. Preferably the photoswitchable binder is caged biotin or a compound in accordance with Formula 1 above.

The aim here is to minimise the formation of any gA-SA-MSL linkages (i.e streptavidin gating). The advantage of this process is that streptavidin gating is reduced and thus the dynamic range is improved. Note an alternative version is that in step (v) the rinsing step can be avoided, meaning that additional SA in step (vi) need not be added.

A method for using photoswitchable linkers during measurement of analyte responses to improve sensitivity by separating any non-specific effect (caused during analyte addition) from the gating response (see Figure 3).

A tethered membrane assembly is made with biotinylated MSL and gA bearing a photoswitchable group derived from a compound in accordance with Formula 1. A biotinylated antibody streptavidin complex is then introduced into the electrolyte solution. The light source is then switched on so that the antibody complex links to the biotinylated MSL but not to the photoswitchable group gA. The analyte is then added and continually stirred and allowed to incubate so that analyte links to MSL via antibody streptavidin biotin complex. (Note at this point there is no crosslinking of MSL to gA or gA to gA because light is on). The solution is then rinsed so that unlinked antibody is removed. An impedance measurement is then made which gives the channel on baseline. Impedance measurements continue and then the light is switched off. The time course of gating is measured as gramicidin crosslinks to MSL via a photoswitchable group streptavidin-biotin-antibody-analyte-antibody-biotin-strepta vidin- photoswitchable group -MSL complex.

The advantages are improved dynamic range due to reduction of streptavidin gating and also an increase in sensitivity as the long incubation time required to crosslink the antibody to MSL no longer limits the rate of change of gating which is carried out rapidly after the crosslinking has occurred (this assumes that off times are significantly longer than on times).

Further, analyte addition artifacts are avoided and thorough mixing can be carried out, and also this method is suitable for optically phase locked loop approaches.

A method for using photoswitchable linkers during measurement of analyte responses to improve sensitivity is shown in Figure 4.

A tethered membrane assembly is made with MSL and gA both bearing a photoswitchable group in accordance with the invention. A

biotinylated antibody streptavidin complex is then introduced into the electrolyte solution. The light source is switched on so that the antibody complex is not bound to either MSL or gA. Analyte is added and continually stirred and allowed to incubate so that analyte crosslinks all antibody- streptavidin complexes. Impedance measurements then commence which gives the channel on baseline Impedance measurements continue and then the light is switched off whilst impedance measurements are made for a further period of time. The time course of gating is measured as gramicidin crosslinks to MSL via a photoswitchable group -streptavidin-biotin-antibody-analyte-antibody-biotin- streptavidin-biotin-MSL complex There are four principal advantages to this method; 1. An amplification in sensitivity is possible where the on rate of the optically switchable group is significantly greater than the on-rate of the antibody to the analyte, and the off times are greater than both, 2. The analyte binding is carried out in three dimensions rather than two, 3. Analyte addition artifacts are avoided and thorough mixing can be carried out, and 4. This method is suitable for optically phase locked loop approaches.

A method for using photoswitchable linkers during measurement of analyte responses to improve sensitivity is shown in Figure 5.

These methods can be modified by using antibodies bearing a photoswitchable group instead of the gA of MSL. In this case the advantages are analyte addition artifacts are avoided and thorough mixing can be carried out, and this method is suitable for optically phase locked loop approaches.

A method for using photoswitchable linkers during measurement of analyte responses to improve sensitivity in a competition assay (such as depicted in figure 6) wherein non-specific effects are separated from the real gating response.

A tethered bilayer employing a gramicidin (or other ion channel) derivative which bears a derivative of the required analyte and a photoswitchable group which binds to streptavidin is produced. A measurement of biosensor impedance is made then the analyte is added. A second measurement is made then a light source is triggered on. A third measurement of the time course response to light is made then the light

source is triggered off. A fourth measurement of the time course response to the removal of light is then made.

The photoswitchable group could of course replace biotin. Such a group may be photoswitchable group or a derivative thereof.

A method for using photoswitchable linkers during measurement of analyte responses to improve sensitivity in a competition assay (such as depicted in figure 7) wherein any non-specific effects (caused during analyte addition) can be separated from the gating response.

A tethered bilayer employing a gramicidin (or other ion channel) derivative which bears a derivative of the required analyte and a photoswitchable group connected to a membrane spanning lipid is produced.

A measurement of biosensor impedance is then made prior to addition of analyte. Analyte is added and a second measurement is made. A light source is then triggered on and a third measurement of the time course response to light is made. The light source is then triggered off and a fourth measurement of the time course response to the removal is made.

A method for using photoswitchable linkers during measurement of analyte responses to improve sensitivity in a lateral segregation assay wherein any non-specific effects (caused during analyte addition) can be separated from the gating response(such as depicted in figure 8).

A tethered bilayer employing a gramicidin (or other ion channel) derivative which bears a derivative of the required analyte and a photoswitchable tether to the bottom layer gramicidin (or other ion channel) is produced. A measurement of biosensor impedance is made and the analyte is added. A second measurement is then made and a light source is triggered on. A third measurement of the time course response to light is made then the light source is triggered off. A fourth measurement of the time course response to the removal is then made.

It will be recognised that a caged biotin could be used in place of a photoswitchable streptavidin ligand such as HABA (or a derivative) in the examples cited above, specifically those depicted in figures 3,4, and 5.

Several caged biotin derivatives are known in the literature, such as those reported by Pirrung (1993, 1996). Such caged derivatives revert to biotin on

irradiation with light and therefore cannot be switched between forms that bind streptavidin and forms that do not bind streptavidin.

An additional example of the use of such caged biotin compounds is depicted in Figure 9.

i) manufacture (e.g. via evaporation) a gold coated substrate on a surface (such as glass or silicon) ii) manufacture a tethered bilayer employing a gramicidin (or other ion channel) derivative which bears a caged biotin iii) streptavidin is added to the system, and attaches to biotin on the MSL4XB iv) a biotinylated receptor is added to the system, and attaches to the SA on MSL4XB v) further biotin is added to block the remaining binding sites on SA vi) a light source is triggered on vii) streptavidin is added to the system, and attaches to newly generated biotin (on the gramicidin) viii) a biotinylated receptor is added to the system, and attaches to the SA on gramicidin ix) analyte is added to the system x) an impedance measurement is made The advantage of this manufacture process is that formation of gA- SA-NISL linkages (i.e. streptavidin gating) is minimised and thus the dynamic range is improved. A further advantage is that receptors can be selected to bind specifically at MSL4XB and the gramicidin derivative, which in turn may improve the response.

Materials and Methods The photoswitchable ligands of the general formulae 1 and 2 are prepared by well known synthetic procedures. For example, the coupling of diazo aromatics with substituted phenols and their derivatives, has been well documented (Berwick 1972; Oku 1979; Weber 1994). It will be recognised that compounds derived from such a coupling reaction can be further functionalised. For example, a free hydroxyl group could be acylated or

etherified using conventional synthetic methods. Representative examples of compounds prepared via these chemical synthetic pathways are depicted in Figure 10.

Preparation of caged biotin - gramicidin complex (gAxx[Bl) A photo-generatable derivative of biotin (so called caged biotin) was prepared by a modification of the method of Pirrung et al (Bioconj. Chem., 1996, 7, 317). This compound (9mg) was dissolved in dichloromethane (5ml) and treated with dicyclohexylcarbodiimide (DCC) (3mg), N-hydroxy succinimide (NHS) (2mg) and dimethylaminopyridine (0.2mg). After stirring at room temperature for two hours a derivative of gramicidin bearing two aminocaproyl groups linked end-to-end and attached to the terminal hydroxyl of gramicidin (prepared by conventional peptide chemistry techniques) was added (30mg, as a solution in methanol (lml) and triethylamine (0.1 ml)). The solution was stirred for 18 hours, evaporated to dryness and then passed through a Sephadex LH-20 column eluting with dichloromethane-methanol-water (800:50:4). The main fraction was then purified by HPLC on a 40mm X 200mm Waters Prep Nova-Pako HR silica column (6calm, 60Å) eluting with dichloromethane-methanol-water (800:40:4) operating at a flow rate of 25ml/min. The fraction, eluting at 24.5 minutes, possessed a 1H-nmr spectrum and mass spectrum in full agreement with the proposed structure.

Investigation of specific photosensitive chemistry in Ion Channel Sensing system Avidin/Streptavidin-biotin chemistry is one of the most widely used reactions in immunochemistry and is the strongest known noncovalent, biological interaction between a protein and a ligand, with KA= l015Ml. The

bond formation is very rapid and once formed, is unaffected by wide extremes of pH, temperature, organic solvents and other denaturing agents.

Conditions which are usually sufficient for denaturing proteins fail to disassociate the avidin-biotin complex. A reporter molecule could be bound to streptavidin covalently, or biotinylated and attached to streptavidin via the streptavidin-biotin interaction. Selective activation and functionalisation of this complex is targeted in this group of experiments.

There are at least two applications that can be identified with the use of photosensitive compounds. The first one is using this chemistry for making the array and the other is for improving the signal by selectively filtering out the non-specific signals and other noise components. Both these applications can be used effectively either independently or together.

The following experiment was conducted with a form of biotin that is not active in the native state (i.e. will not bind to streptavidin) but can be activated by uV irradiation to bind streptavidin. This photoactivable form of biotin has been conjugated with gramicidin and used as an essential component of the bilayer membrane for targeting chemistries using streptavidin-biotin complex.

Materials and methods: Preparation of electrodes: The gold electrodes were built on commercially available glass microscope slides. The glass slides were cleaned for 2 hours in the glass cleaning solution "Extran 300", rinsed several times with copious volumes of deionised water and dried in a stream of nitrogen in clean room conditions.

The metal deposition was carried out using an Edwards evaporation unit. An adhesion layer of chromium (~20no) was deposited followed by a layer of gold (100nM). One side of the glass slides was fully coated with metal. The metal treated glass slides were removed from the evaporator and quickly immersed in an ethanolic solution of monolayer components for an hour (AM300), rinsed profusely in ethanol and preserved in ethanol. These electrodes were stored at 40C for 24 hours before assembling the second layer of the membrane.

Preparation of reagents and biomolecules: Preparation of solutions of test compound and control compounds.

The photoactivable biotin in its native form has a molecular weight of 686d and has a molecular weight of 2.809kd in the form of gAxx[B]. This compound was dissolved in ethanol to prepare a 2mM solution (5.5mg in 1.958ml) and further diluted to a lOuM solution. An aliquot of the gAxx[B] solution was activated by irradiating the solution at 350nM for a period of 20 minutes.

Three types of second layer membrane solutions were prepared with 3mM lipids DPEPC (1,2-di(3RS, 7R, 11R-phytanyl)-glycero-3-phosphocholine) and GDPE (1,2-di(3RS, 7R, 11R-phytanyl)-glycerol) in 7:3 ratio and three types of gA5xB. The first solution was prepared with gA5xB (see Figure 11), the second with the inactive form of photoactivatable gAxx[B] and the third solution with the activated form of photoactivatable gAxx[B].

Streptavidin was diluted in PBS to a concentration of O.lmg/ml. The matched pair of biotinylated Thyroid Stimulating Hormone (TSH) Fabs (E20650M and E45650M) was combined in equal molar ratio to give a 50ug/ml solution in PBS. TSH analyte was diluted in chilled PBS to prepare a 2.5nM solution.

Assembling biosensor blocks: The monolayer AM300 was deposited on metallised glass electrodes as per established protocol. The electrodes were assembled into biosensor blocks. The second layer solution was added manually (15Fl per cell) and washed five times with PBS to assemble the bilayer membrane. The fully assembled blocks had the following second layers: Block 1: Row A (cells 1-8) with a ratio of 40k: 1 standard gA5xB Row B (cells 9-16) with a ratio of 40k: 1 inactive for of gAxx[B] Block 2: Same as above Block 3: Row A (cells 1-8) with standard gA5xB as in blocks 1 and 2 Row B (cells 9-16) with the activated form of gAxx[B].

A second group of 2 blocks were assembled with the inactive form of gAxx[B] and the cells were exposed to uV irradiation. The exposure time for pairs of cells was varied to study the effects of time length of exposure and

select the most effective time period for future experiments. Exposure times down to one minute were found to be effective.

Observations: The inactive form of gAxx[B] did not show a binding response when treated with 42nM streptavidin. This was reproducible and the positive control used in cells could be continued further to complete the TSH assay, The activated form showed moderate response when exposed to streptavidin.

Cells 1-8 used the standard composition of second layer as a positive control for comparison and these responded to streptavidin. Cells 9-16 using the inactive form of gAxx[B] showed no response when exposed to streptavidin.

In the time course measurements the inactive gAxx[B] did not appear to facilitate a specific response as compared to the specific response elicited with standard gA5x[B].

Determination of the impedance responses showed that the activated form of gAxx[B] (test cells 9-16) showed a positive response to the addition of streptavidin. The inactive from of gAxx[B] did not facilitate any specific response. It may be concluded from these experiments that photoactivable gAxx[B] can be effectively activated by ultra violet irradiation to actively bind to streptavidin and allow gating of the biosensor.

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 the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.

References: 1. Pirrung et al, j Am. Chem. Soc., 1993, 115, 12050 ; Pirrung et al, Bioconj. Chem. 1996, 7, 137.

2. Berwick et al., J. Org. Chem., 1972, 37, 2409.

3. Oku et al., J. Org. Chem., 1979, 44, 3342.

4. Weber et al, J. Am. Chem. Soc., 1994, 116, 2717.

5. Pillai, Sythesis, 1980, 1