Patent Application
20070132831
1. Field of the Invention
This invention relates to scanning systems for microarrays of biological species such as nucleic acids and proteins, and in general to illumination systems for any type of procedure that involves the individual and sequential illumination of a large number of sites arranged in a spatial array.
2. Description of the Prior Art
Microarrays are two-dimensional arrays of sites where chemical or biochemical assays are performed, each site often being of microscopic dimensions, with an independent assay and often a different molecular species at each site. Microarrays are formed on a variety of substrates, including glass slides, microtiter plates, and membranes. Microarrays are commonly used for example in binding assays for identifying, determining the binding affinity of, or otherwise characterizing unknown biological species. The size, number and spacing of the sites in a microarray can vary considerably. When the sites are wells in a standard microtiter plate, the wells will be 96 in number in a 12×8 array with a spacing between wells of 9 mm. When the sites are spots applied to a glass slide, which is typically 25 mm in width, by automated microprinting techniques, the number of sites can be in the thousands. For gene assays, a single glass slide will typically contain as many as 10,000 genes.
Imaging of the microarray for purposes of monitoring and detection of each assay is achieved by scanning, and in many methodologies, the scanning process includes illumination of each site of the microarray with excitation light. To accomplish this, the scanner head moves in reciprocating strokes across the microarray, each stroke having a velocity profile that includes deceleration at each end of the stroke prior to the reversal of direction, followed by an acceleration after the reversal of direction to bring the head back up to speed for the next stroke. Excitation is typically achieved by a laser which, to serve as a stable light source, is preferably left on for the entire duration of the scan. If sites of the microarray extend to the ends of the path of travel of the scanner head, the use of an uninterrupted laser beam can cause certain sites to receive greater exposure than others. This can lead to overexposure or photobleaching of the site contents. In addition, regardless of whether the laser beam is left on continuously or turned off at the ends of each stroke, a certain degree of light spillage to adjacent wells occurs, either by diffusion, reflection or refraction, when the laser is focused on any single well. Light spillage of this nature can occur between rows as well as within a row, particularly when the path of travel of the scanner head exceeds the width of the row. Light spillage can also occur when a single stroke covers only a portion of a row, with spillage onto portions of the row that are not being scanned. In all cases, the spillage causes undesirable overexposure or generates background noise among the scanning signals, or both.
These and other limitations of the prior art are addressed by the present invention, which resides in a microarray scanning illumination system that includes a sample support, a reciprocating-motion scan head, and a mask positioned between the sample support and the scan head, the mask blocking all light from passing from the scan head to the sample support other than through an opening in the mask that exposes only the sites to be scanned in a single stroke of the scan head or a series of parallel strokes. Defining the scanning direction along a single row as the x-axis, the width of the opening parallel to the x-axis in certain embodiments of the invention is sufficient to expose more than one, but less than all, of the sample sites in a row, and is shorter in length than the path of travel of the scan head in a single stroke of the reciprocating movement of the scan head. With the mask appropriately sized and positioned, light from the scan head will be blocked and thus prevented from reaching the microarray at the two ends of the path of travel where the scan head is decelerating or accelerating to reverse its direction. In certain embodiments as well, the mask can also be sized and positioned to expose only one row, or a portion of only one row, of sites in the microarray, thereby preventing spillage of light onto adjacent rows. The mask is particularly useful when the scan head traverses only a portion of a row in a single stroke but can be shifted to another portion or the remainder of the row at a later stage of the imaging process to complete a scan of the entire row. In general, the present invention resides in the use of the mask to prevent the unwanted illumination of sites not being scanned, or to prevent nonuniform exposure of sites due to the end effects of the reciprocating motion of the scan head, or to prevent both. In all cases, the mask is movable relative to the microarray, or vice versa, to expose different groups of sites to the scan head as needed to provide a complete scan of the microarray.
These and other objects, features, advantages, and embodiments of the invention will become apparent from the description that follows.
The sequence in which the sites of the microarray are illuminated by the light source during the scanning process path is referred to herein as the scanning protocol, and is determined by the length of each stroke of the scan head (to which the light source is affixed) during the reciprocating, i.e., back-and-forth, motion of the scan head, in conjunction with the incremental movements of the microarray to align the scan head with successive rows of sample sites on the microarray and all other movements of the scan head, mask, and microarray needed to complete the scanning of the entire microarray. While individual protocols can vary depending on the configuration and dimensions of the microarray, all protocols will include reciprocating motion of the scan head along the x-axis for each row of the microarray. While a uniform scan head speed would provide the most even distribution of illumination among the sample sites along the path of travel, absolute uniformity is not achievable. Instead, because the scan head driver must reverse the direction of the scan head at each end of its path of travel, reciprocating scan heads undergo a deceleration at each end of each stroke followed by acceleration in the reverse direction. Typical of the drivers used for scan heads are moving coil actuators, which utilize the well-known Lorentz force that results from an alternating current passing through an electric coil in a magnetic field. Moving coil actuators are also referred to as voice coil actuators, and examples of these actuators that are in current use are those supplied by the Kimco Magnetics Divison of BEI Technologies, Inc., San Marcos, Calif., USA, and by H2W Technologies, Inc., Valencia, Calif., USA. Disclosures of voice coil actuators are found in U.S. Pat. Nos. 6,894,408, 6,870,285, 6,815,846, and 6,787,943. Further voice coil actuators are described in commonly owned, co-pending U.S. patent application Ser. No. 11/265,000, filed Nov. 1, 2005, inventors Paul J. Patt et al., entitled “Moving Coil Actuator for Reciprocating Motion With Controlled Force Distribution,” and commonly owned, co-pending U.S. patent application Ser. No. 11/______, filed Nov. 30, 2005, inventor Daniel Y. Chu, entitled “Moving Coil Actuator with Expandable Range of Motion.” The contents of each of these documents are incorporated herein by reference. In scanning systems that incorporate any of these actuators, movement of the scan head is caused by movement of the coil which itself is a response to an electromagnetic force. While the velocity profile over the path of travel of the coil will vary with the magnitude of the electric potential, the configuration of the coil, and the sizes and relative positions of the coil and the magnet, the profiles for all such coils include deceleration and acceleration at the limits of travel, as noted above, for each row.
The travel path of the scan head during one stroke of the reciprocating motion is shown in
The mask 23 is positioned between the scan head 12 and the microarray 11, and preferably between the scan head 12 and the focusing lens 13 to obtain maximal benefit of the short focal length of the lens. The mask has a window or opening 24 that is centered between the two ends 21, 22 of the trajectory of the scan head. The width of the window 24 in this embodiment is approximately equal to the width of the central portion of the trajectory in which the velocity is at its target value. As a result, the scan head 12 and lens 13 are aligned with the window 24 only when the scan head and lens are moving at the target velocity, and all sites of the microarray that are not blocked by the mask 24 will be illuminated uniformly for a uniform duration of time since the scan head and lens pass each one at the same speed. The mask thus eliminates the overexposure that is achieved during the portions of the scan head travel in which deceleration and acceleration occur.
While the reciprocating motion is along the x-axis within individual rows, scanning of different rows in succession is achieved by incremental advances along the y-axis between strokes along the x-axis. The y-axis advances can be achieved by moving either the microarray or the scan head, actuator and mask. While scanning profiles can vary, the typical and preferred profile begins with a scan of sites in one row in a single direction along the x-axis, followed by an incremental advance of the microarray or scanning head along the y-axis to the next adjacent row, followed by a scan of sites of the new row along the x-axis in the direction opposite to that of the scan in the first row. The rows are thus scanned in alternating directions along the x-axis with incremental advances along the y-axis between each x-axis scan. For this scanning protocol, the mask window 24 can be just large enough to expose sites within only one row, requiring the mask and scanner to be moved together along the y-axis between each single row scan. Alternatively, the mask window 24 can be large enough to expose sites of two or more adjacent rows simultaneously, in which case the mask need only be moved after all rows exposed by the window have been scanned.
While the blocking of the scan head during acceleration and deceleration eliminates overexposure, a mask in accordance with this invention will also reduce or eliminate light spillage to sites not being scanned in a particular stroke. Light spillage arises in adjacent rows when a particular row is being scanned and also in adjacent portions of the same row when only a portion of a row is being scanned.
In the views shown in
The mask in each of these embodiments can be constructed of conventional materials well known among those skilled in the art. Any material that is non-transmissive and non-reflective of light can be used, and the window can either be an opening (i.e., a void), or a transparent material. The mask can be rigidly secured to the scan driver so that the two move together while allowing the scan head and lens to move relative to the mask. Alternatively, the mask can be independently movable.
As noted above, moving coil actuators are preferred as drivers for the scan head. Scanning systems with relatively short scan distances that are capable of scanning portions of rows as illustrated by
Further variations and embodiments will be apparent to those skilled in the art of microarray scanning who have studied the drawings and descriptions offered above. In addition to variations in the configurations and geometries of the mask, scan head and driver, for example, a variety of scanning protocols and operating conditions, all within the scope of this invention, will be readily apparent to the skilled engineer.
