Analytical apparatus

Details Analytical apparatus Analytical apparatus

2001-06-21

2004-02-17

Chin, Christopher L. (Department: 1641)

Chemistry: analytical and immunological testing

Involving an insoluble carrier for immobilizing immunochemicals

C356S317000, C356S318000, C356S320000, C385S012000, C385S129000, C385S130000, C422S051000, C422S051000, C422S068100, C422S082110, C435S007100, C435S287100, C435S287200, C435S287900, C435S288700, C435S808000, C436S164000, C436S165000, C436S524000, C436S525000, C436S805000

Reexamination Certificate

active

06692974

ABSTRACT:

TECHNICAL FIELD
The present invention relates broadly to apparatus for the detection of analytes. The invention further relates to methods employing such apparatus.
BACKGROUND ART
The use of Surface Plasmon Resonance (SPR) for the detection of small soluble analytes from solution is well known (see e.g. “Advances in Biosensors—A Research Annual Vol 1. 1991” Ed. A P F Turner, Pub. Jai Press Ltd, London).
Briefly, an SPR apparatus generally comprises a light source for generating polarised light; a sensor, the outside of which is metal coated and may be contacted with a sample solution, and means for detecting the light which is internally reflected from the inner sensor surface.
In the absence of bound analyte, light is totally internally reflected at an incident angle characteristic of the refractive index (RI) of the sensor and of the sample solution. At a particular incident angle (the ‘SPR angle’), interaction of the metal with the evanescent wave set up by internal reflection of the polarised light causes a drop in intensity of the reflected light. This drop can be observed using the light detector.
The binding of analyte to the sensor surface, within the evanescent wave zone, alters the RI of the sensor and this perturbs the SPR angle. This perturbation can be observed using the light sensor and related to the surface concentration of analyte.
SPR detection in the literature has generally been limited to use with soluble molecular size analytes e.g. biomolecules such as proteins and nucleic acids which are specifically bound within the evanescent zone using appropriate ligands.
However, the SPR apparatus in the art to date has not been suitable for accurately detecting sample materials with both soluble and insoluble analytes therein. In particular, due to the more limited way in which (for instance) roughly spherical cells of several &mgr;m diameter interact with the evanescent zone, only fairly high concentrations (e.g. 10
7
-10
8
/ml) have been detectable using SPR. Thus in order to detect cells, as opposed to (for instance) protein antigens, further apparatus, and hence more cost, time and experimentation, have been required. For instance cells have frequently been detected using culture techniques followed by specific detection.
DISCLOSURE OF THE INVENTION
1. A surface plasmon resonance apparatus for detecting single particulate analytes, the apparatus comprising:
(a) a sensor, or means to receive a sensor, said sensor providing a metallised surface capable of binding the analyte;
(b) a light source capable of generating an evanescent wave at the sensor surface;
(c) a detector capable of detecting light scatterered or emitted from a single particulate analyte bound at the sensor surface, said detector being located on the opposite side of the sensor surface to which light from said source is incident.
Suitable sensors are slides.
Possible analytes may include those particulate or insoluble analytes containing or consisting of biomolecules, for instance bacteria or other cells, spores, viruses or virions etc., or biomolecules themselves such as proteins or polynucleotides. Possible bacterial targets include
cryptosporidium, E. coli, salmonella
etc.
The apparatus may thus be used with a wide variety of samples suspected or known to contain analytes. For examples environmental samples such as water, or biological samples.
Broadly speaking the apparatus operates as follows: in use the second detector detects the binding of soluble analytes to the sensor surface by detecting the changes in the intensity of light internally reflected from the sensor surface, whereas the first detector detects the binding of particulate analytes to the sensor surface by detecting the light scattered or emitted from the analytes bound thereto. The apparatus of the present invention is therefore capable of the sensitive detection of both soluble and particulate analytes, and thus may provide a quicker, cheaper or more sensitive alternative to the methods and apparatus presently used in the art.
It is important to stress the different functions of the detectors in the apparatus. The second detector must be arranged to detect light internally reflected from the sensor surface, the intensity of this light being dependent on the SPR effects occurring as analytes (especially soluble ones) bind at the sensor surface altering the refractive index of the sensor/sample interface. The detector may be a 2-D array detector as described in more detail in the Examples below.
By contrast the fist detector detects light which is scattered or otherwise emitted (optionally by fluorescence) from analytes (especially particulate ones) which interact with the evanescent field at the sensor surface. This may give a sensitivity for detecting large particulate analytes several orders of magnitude higher than would be obtainable using pure SPR. Clearly the nature of the first detector used will determine the sensitivity and acuity of the detection, but in preferred embodiments single cells bound within the evanescence zone may be detected and resolved using the first detector while the bulk binding effects of soluble molecules may be detected using the first.
Preferably the first detector is a video camera (e.g. a Charge Coupled Detector [CCD] camera), but any kind of light detector appropriated for detecting light scattered or emitted from the analytes may be used e.g. a 2-D diode array, a photomultiplier etc.
In one embodiment the first detector is located on the same side of the surface as the light source such as to be capable of detecting light which is back-scattered or emitted when an analyte is bound to thereto.
The term ‘light source’ as used herein means any source of light radiation, including where appropriate the tip of an optical fibre which is attached to a remote radiation source.
In a different embodiment, the first detector is located on the opposite side of the surface as the light source detector such as to be capable of detecting light which is scattered or emitted when an analyte is bound to thereto.
In either case it may be desirable that the first detector is located such as to be capable of detecting light scattered or emitted at a predetermined angle, for example substantially normally, to the sensor surface. This will minimise interference from light which is being totally internally reflected from the surface.
Generally the sensor block will comprise a prism or a hemicylinder, such as are known to those skilled in the art of SPR detection. The sensor block is adapted to receive the detachable sensor which provides the metallised surface. The adaptation may simply consist of providing a general area to mount the sensor such as a slide, or the block may be specially shaped or configured to receive it e.g. in a groove or properly-dimensioned well.
The block and or sensor may in addition be adapted to form all or part of one wall of a flow channel, through which a liquid sample can flow in liquid contact with the metallised surface. An apparatus comprising such a flow channel forms one embodiment of the first aspect of the invention.
Preferably the metallised sensor surface is adapted or otherwise functionalised such as to facilitate the immobilisation of macromolecules which are capable of specifically binding biomolecules thereto. For instance the sensor may have a hydrophilic dextran surface. Antibodies may then be immobilised thereto in order to specifically bind antigenic analytes. Alternatively a polynucleotide probe may be immobilised for specifically binding a polynucleotide analytes.
Preferably the e.g. antibodies are bound only to discrete portions of surface in order to facilitate the detecting light which is scattered or emitted when an analyte is bound to thereto. These portions may then be visualised (and possibly further resolved) by the second detector as contrasting discrete bright areas against the darker portions of the surface which do not have macromolecules bound to them.
The surface may have greater then one type of macromolecule immobilised thereto for spec

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