Patent Application
20050135974
(1) Field of the Invention
The present invention relates to a device for preparing assay samples using a number of microscope slides. Each slide has a number of assay reaction surface locations spaced on the planar surface of the slide. In preferred embodiments, the device comprises, in part, a microscope slide holder that has the exterior dimensions of a SBS standard microplate, such as a 96 well plate. The device accepts conventional microscope slides equipped with sixteen microarray surfaces spaced nine millimeters apart on center, or four for a 96 well plate. Individual chamber plates are placed on top of the slides, creating an individual well above each assay reaction surface location. In preferred embodiments, each assay reaction surface location can comprise a microarray of multiple reactive sites. Thus, parallel processing can be done of samples for genomic or proteomic profiling. An advantage of the present invention is that one can use the conventional high throughput assaying equipment for SBS standard microplates while using conventional microscope slides, thereby allowing the use of robotic assay reading equipment designed for slides.
(2) Description of the Related Art, Including Information Disclosed Under 37 CFR 1.97 & 1.98
Multiwell test plates (otherwise referred to in the art as either microtiterplates or microplates) are essential tools for scientists looking to assay many samples at a time. In an effort to provide more flexibility to microplates, the art has incorporated various features. As seen in U.S. Pat. No. 5,679,310, the microplate has been modified to include high surface area structure on the bottom interior of the wells. It has also been modified to use a porous separation medium at the bottom interior of the well so as to facilitate separation of liquids from solids in samples (see U.S. Pat. No. 5,417,923). Gasketed tops have been added to microplates to prevent cross contamination of samples (see U.S. Pat. No. 5,516,490).
With the development of genomics and proteomics, technologies are required that permit the automated processing of large numbers of samples that are interrogated with a large number of binding elements. Microchip technologies have provided numerous solutions that allow investigators to determine multiple reactivities within a given biological sample.
DNA and protein microarrays have become important methods to allow the simultaneous interrogation of multiple binding reactions (cf. Schena, M. et al., Science 270:467-469(1995), Duggan, D. J., et al., Nature Genetics 21:10-14,(1999), MacBeath, G. and Schrieber, S. L. Science 289:1760-1763(2000). Testing multiple samples at the same time for binding activity against all the elements of a given array significantly increases the power of parallel processing with minimal sample volumes.
For example Schena et. Al describe immobilizing large numbers of oligonucleotides, representing genomic sequences, to a glass microscope slide and hybridizing probes made from the total RNA of a cell to these sequences. This provides, in one binding experiment, a view of all the genes expressed in that cell at that point in time. Similar microarrays have been described using large numbers of antibodies immobilized on glass slides to understand which proteins, and in what quantity, are expressed in a cell or group of cells at a particular point in time. The generation of these microarrays is dependent, in part, on spotting robots able to deliver small volumes of samples to precise locations on the glass slide.
Methods and devices to provide and improve high throughput analysis of biomolecules (nucleic acids, proteins etc.) are important for elucidation of protein function, diagnostic testing, drug discovery and drug target identification. One set of technologies that have improved the simultaneous interrogation of large numbers of biomolecules is the use of microarrays. Microarrays are ordered displays of molecules generally immobilized on a surface. Such an array permits the simultaneous investigation of binding of many elements to target molecules. A variety of technologies have been developed to allow investigators to make, process and detect reactions on microarrays.
An object of the invention is to provide addressable protein microarrays on a surface that binds many different proteins, maintains the protein three dimensional structure, and immobilizes them in sufficient quantity to allow for sensitive detection.
A second object of the invention is to be able to interrogate sensitively the same array of proteins with different samples or binding partners. Because specific protein binding partners are generally rare, any technique which allows the use of minimum quantities is preferred.
A third object of the invention is to use a convenient set of methodologies to allow high throughput techniques. In particular, an object of the invention is to use the “micro plate” 96 well format, which is based on 9 mm spacings of reaction areas which are 7 mm either in diameter or square. Many pipetting aids, detection instrumentation, liquid handling systems and robotics have been designed to conform to this format.
A fourth object of the present invention is to provide for parallel processing of substantially identical microarrays on multiple samples.
A fifth object of the present invention is to provide a device that can take a microscope slide based reaction surface and convert it for use with conventional microplate-based, high throughput robotic equipment.
In essence, what microarrays allow is the accumulation of large amounts of data due to parallel processing. To this point in time this has largely been accomplished by subjecting single biological samples to large numbers of binding elements. If multiple samples could be processed against multiple arrays the amount of information would increase. This is particularly important in drug discovery, diagnostic and prognostic applications of microarrays where simultaneous screening of multiple samples is essential for quality comparative results.
The present invention is a device for preparing multiple assay samples for multiple reactive sites located on at least one assay slide. Each slide comprises a planar support having a set of exterior edges and a planar surface covered with a plurality of separate and discretely spaced assay reaction surface locations. Each assay reaction surface location is treated so as to provide a reaction surface for a sample that is to be assayed for a genomic or proteomic activity. Conventional reagents well known to those of skill in the art can be used for such reactions, including proteins and nucleic acids, typically derived from sequences occurring in cells and tissues. Each assay location must have at least one assay reaction site, but typically can have a plurality of assay reaction sites per assay surface location, possibly hundreds of assay reaction sites. The assay location surfaces are present at a density of at least eight per eighteen square centimeters.
Along with the slides, the present invention comprises at least one planar multiwell chamber plates. Each chamber plate has a plurality of bottomless wells located between a top planar surface and a bottom planar surface and encompassed by a set of exterior wall surfaces. Each chamber plate is dimensioned and configured so as to register the wells with the assay reaction surface locations of a corresponding assay slide. Each chamber plate is located adjacent to and in registration with the corresponding assay slide. Each chamber plate well is dimensioned so as to encompass the area of a corresponding assay reaction surface location on the corresponding assay slide. Each well is discrete from the other and is dimensioned so as to receive a sample. Each well has an opening that can communicate with the corresponding assay reaction surface location.
A slide holder equipped with a plurality of slide openings holds the slides. Each slide opening is dimensioned and configured so as to receive an assay slide. In some embodiments the opening is in a horizontal surface of the slide holder and is designed to receive slides from a vertical movement (see
The present invention also can comprise the use of a top for a securing means. As seen in
The present invention also can combine a top and the chamber plates into a unitary structure, as seen in
The instant devices can be used in methods for processing multiple assay samples. Typically, one would add a sample to at least one prepared well in at least one chamber plate and corresponding slide in any of the above devices. The assay reaction surface location can be prepared either with the slide in the slide holder or before the slide is placed in the slide holder. Typically, one would apply a plurality of samples to each slide, each to a respective assay reaction surface location. In cases where parallel processing is desired, one would have a substantially identical set of assay reaction sites on each slide.
Using conventional parameters, one reacts the sample with the assay reaction surface location in the well.
Finally, one measures the signal from the reacted sample using conventional signal measurement techniques appropriate for the selected signal chemistries. In some cases, after reacting the sample with the prepared surface, one will need to perform at least one additional reaction to produce the measurable signal. The signal can be measured with the slide either in the slide holder or removed from the slide holder. The signal can be measured by a conventional robotic signal measurement means. If parallel processing is desired for the slides, then one compares the signal from the samples so as to identify redundant reaction patterns that indicate any similarities within the samples Suitable samples include proteomic or genomic samples such as is selected from the group consisting of cell lysates, cell supernatants, plasma, serum, or biological fluids.
In preferred embodiments, the present invention relates to a device for preparing multiple assay samples (10). A first preferred embodiment is shown in
As seen in the Figures, the present invention also comprises four planar multiwell chamber plates (30) that are dimensioned to have the same planar area as the corresponding slides. Each chamber plate comprises sixteen bottomless wells (32) located between a top planar surface (34) and a bottom planar surface (36) and encompassed by a set of exterior wall surfaces (38). Each chamber plate is dimensioned and configured so as to allow the wells to be registerable with the assay location surfaces (26) of the microarray assay slide (20). Each chamber plate is located adjacent to and in registration with a corresponding assay slide. Each well is dimensioned to encompass the area of a corresponding assay reaction surface location on the corresponding assay slide, each well is discrete from the other and is dimensioned so as to receive a sample, and each well has an opening that can communicate with the corresponding assay location surface.
The chamber plate can be made of a material that is inert to any reaction that is to take place within the well and has an elastomeric nature, such as silicone rubber. The chamber plate can be releaseably secured to the corresponding slide by a releaseable sealing means located on the bottom planar surface of the chamber plate such that each slide can be releaseably engaged with the chamber plate, such as conventional releasable adhesives.
The present invention also comprises a slide holder (40) having four slide openings (42). Each slide opening is dimensioned and configured so as to receive an assay slide. Shoulders about the opening (44) support each slide in a registerable position. In addition, each slide opening can have one wall that slopes inward from an exterior wall of the slide holder such that the upper portion of the opening has an area less than that of the slide, thereby requiring the slide to be tilted in order to be received within the opening.
Suitable materials for the slide holder element of the present invention are conventional and known to those of skill in the art. Examples include acetal, polypropylene, PTFE, aluminum, stainless steel, polystyrene, or acrylics.
Finally, the present invention can have a slide retention means (50) attached to the slide holder. The slide retention means can be a spring-loaded depressable ball means (52) or a moveable protusion means. The slide retention means functions so as to allow each slide and corresponding chamber plate to be received in the corresponding opening in the slide holder, and yet be retained within the opening once seated in the opening.
A second preferred embodiment of the present invention uses a lid to secure the chamber plate and microscope slide to the slide holder. As seen in
The second preferred embodiment can include many of the optional features of the first preferred embodiment, including a releaseable sealing means located on the bottom planar surface of the chamber plate such that each slide can be releaseably engaged with the chamber plate, each opening in the slide holder has one wall that slopes inward from an exterior wall of the slide holder such that the upper portion of the opening has an area less than that of the slide, thereby requiring the microarray slide to be tilted in order to be received within the opening, each assay slide has the same dimensions along the exterior edges and the planar surface, each slide has the same set of assay reaction surface locations.
A third preferred embodiment is shown in
A fourth preferred embodiment is shown in FIGS. 7 to 9. Like the first preferred embodiment, the slide retention means is located in the slide holder. However, unlike the first preferred embodiment, the slide retention means (spring-loaded depressable ball 52) is located in a vertical operating position. Moreover, the slide holder has a slide opening (42) in the vertical exterior wall. Along with the shoulders (44) about the slide opening, flanges (54) are located along the upper surface so as to keep each slide from being removed by a horizontal movement. This structure permits a slide to be positioned in the slide holder with a horizontal movement that stops when one end of the slide engages the distal end of the slide opening, the spring loaded ball then being free of the slide at the proximal end of the slide opening.
A fifth preferred embodiment is shown in
In all of these embodiments, the microarray sample device can have a plurality of assay reaction sites at each assay reaction surface location. The reaction sites can be grouped so as to form a microarray at each assay surface reaction location.
In all of these embodiments, the microarray sample device can have at least two assay surface locations have the substantially identical pattern of assay reaction sites.
Sixteen pad FAST brand slides (made by Schleicher and Schuell BioScience, Inc. of Keene, N.H., USA) were arrayed with commercially available anti-IL6 antibody at concentrations of 1 mg/ml, 0.5 mg/ml, 0.25 mg/ml and buffer only using a Perker Elmer BioChip Arrayer (made by Perkin Elmer of Boston, Mass. The arrayed slides were placed in a slide holder as shown in
The slides were blocked for 15 minutes in 70 ul/well of a blocking buffer (1× Tris buffered saline (TBS), 2% Tween20 surfactant, 0.1% polyvinyl pyrriladone, and 0.5% polyvinyl alcohol). The blocking buffer was removed using the liquid handler. A solution of 1 mg/ml IL6 antigen in RPMI with 10% fetal calf serum was added to the well at 70 ul/well. The slides were incubated with antigen for 1 hour while rotating the slide holder.
After a first incubation, the antigen solution was removed and the slides were washed 3 times with 70 ul wash buffer (1× TBS and 0.1% Tween20 surfactant) by dispensing the buffer, pipetting up and down 3× and removing buffer with the liquid handler. The slides were incubated with 70 ul of biotinylated anti-IL6 antibody at a concentration of 100 ng/ml for 1 hour while rotating the slide holder.
After a second incubation, the slides were washed again as described above. A solution of streptavidin-Cy5 (a 1:8000 dilution of a 1 mg/ml stock) was added to the wells at 70 ul/well. The slides were incubated at 1 hour while rotating the slide holder. The slides were then washed again as described above, dried at 80 C for approximately 1 minute and scanned using a GSI Lumonics ScanArray 4000 scanner at laser PMT settings of 85:50 (made by Perkin Elmer of Boston, Mass.). All of the slides could be read as if processed individually.
As shown in
The left hand image shows IL-1b expression is increased in LPS-treated cells, while the right hand image shows IL-8 expression also is increased in LPS-treated cells. All transfer steps are performed using automated liquid handling.
The images in
The ordinarily skilled artisan can appreciate that the present invention can incorporate any number of the preferred features described above.
All publications or unpublished patent applications mentioned herein are hereby incorporated by reference thereto.
Other embodiments of the present invention are not presented here which are obvious to those of ordinary skill in the art, now or during the term of any patent issuing from this patent specification, and thus, are within the spirit and scope of the present invention.
