Patent Application
20190345429
This invention relates to the filed of biology, and more particularly, to devices for holding single cells for enabling experiments to be performed in the cells.
Delivery of molecules, DNAs and proteins into the cytoplasm of a cell is essential for cell-based research and development as well as clinical application such as drug screening and in vitro fertilization. Microinjection is one of the most precise techniques to inject cargo materials into the single cells or to remove cellular organelles. Motorized translation stages with high-resolution and high-precision in combination with microinjectors precisely control the position of injection needle, which punctate cell membrane and dispense predetermined volume of the cargo materials into the cells. The precision and controllability make the microinjection technique stand out from other delivery methods such as electroporation and viral transduction.
Microinjection techniques, however, requires well trained personnel. The success rate of injection highly depends to the operator's skill. Typically, it takes 15-30 s of operation time for microinjection per cell for a skilled operator. During the injection, even small movement will punctuate large hole on the cell membrane, which can lead to cell apoptosis.
The inventors have found that restraining cell movement by a cell holding device during the injection can minimize damage to the cell membrane and to diminish the time required for successfully perform a microinjection.
To address the issues of current microinjection techniques, the present invention relates to a device configured to hold a plurality single cells in an array and restrain cell movement during injection. Traditional injection methods require to hold a cell manually with one arm and operate the injector with the other arm, followed by release of the cell. In the device of the present invention, microwells are provided such that each microwell holds a single cell. Each microwell is shaped to anchor the cell to the microwell and to restrain movement during injection and textured surface.
By using the device of the present invention, the need of cell holding arm is obviated. This makes microinjection process faster and less skill dependent. In some embodiments of the present invention, the microwells isolate the cells in pre-defined positions. This enables automation of injection and tracking of the individual cells.
An aspect of some embodiments of the present invention relates to a device for holding a plurality of cells, the device comprising a top layer having a plurality of spaced apart microwells which are not in contact with each other, each microwell being open on top and sized to hold a single cell. Each microwell has a top cross sectional shape having a perimeter which includes at least one inner concave angle and at least one inner convex angle, for providing increased friction between the microwell and the cell contained within.
In a variant, the at least one inner convex angle is acute.
In another variant, the at least one of the microwells has the top cross-sectional shape having the perimeter which includes a plurality of inner concave angles and a plurality of inner convex angle, such that a plurality of extensions are formed, protruding inward from the perimeter, to provide increased friction between the microwell and the cell contained within.
In some embodiments of the present invention, at least one of the inner convex angles is acute.
In yet another variant, the top layer is transparent to visible light.
In a further variant, the device further comprises a substrate bonded to a bottom of the top layer.
In a variant, the substrate is rigid.
In another variant, the substrate is made of material that is transparent to visible light.
In yet another variant, at least one of the microwells is open on both the top and bottom of the top layer, and the substrate closes the at least one of the microwells at the bottom of the top layer.
In a further variant, the microwells are arranged to form an array of rows parallel to each other and of rows parallel to each other.
Each row may be perpendicular to the columns.
In yet a further variant, the top layer comprises at least one depression having a floor. The at least one depression comprises at least one respective microwell notched on the floor.
In a variant, each depression comprises a plurality of respective microwells notched on the respective floor of the depression.
In another variant all microwells are notched on the floor of the at least one depression.
In yet another variant, the top layer comprises at least two depressions spaced apart from each other and not in communication with each other, each depression having a respective floor. Each depression comprises at least one respective microwell notched on the respective floor of the depression.
In a further variant, each depression comprises a plurality of respective microwells notched on the respective floor of the depression.
In yet a further variant, all microwells are notched on the floors the at least two depressions.
In some embodiments of the present invention, the device of some embodiments the present invention is shaped as a microscope slide.
Other features and aspects of the invention will become apparent from the following detailed description, taken in conjunction with the accompanying drawings, which illustrate, by way of example, the features in accordance with embodiments of the invention. The summary is not intended to limit the scope of the invention, which is defined solely by the claims attached hereto.
The present invention, in accordance with one or more various embodiments, is described in detail with reference to the following figures. The drawings are provided for purposes of illustration only and merely depict typical or example embodiments of the invention. These drawings are provided to facilitate the reader's understanding of the invention and shall not be considered limiting of the breadth, scope, or applicability of the invention. It should be noted that for clarity and ease of illustration these drawings are not necessarily made to scale.
Some of the figures included herein illustrate various embodiments of the invention from different viewing angles. Although the accompanying descriptive text may refer to such views as “top,” “bottom” or “side” views, such references are merely descriptive and do not imply or require that the invention be implemented or used in a particular spatial orientation unless explicitly stated otherwise.
It should be understood that the invention can be practiced with modification and alteration, and that the invention be limited only by the claims and the equivalents thereof.
From time-to-time, the present invention is described herein in terms of example environments. Description in terms of these environments is provided to allow the various features and embodiments of the invention to be portrayed in the context of an exemplary application. After reading this description, it will become apparent to one of ordinary skill in the art how the invention can be implemented in different and alternative environments.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art to which this invention belongs. All patents, applications, published applications and other publications referred to herein are incorporated by reference in their entirety. If a definition set forth in this section is contrary to or otherwise inconsistent with a definition set forth in applications, published applications and other publications that are herein incorporated by reference, the definition set forth in this document prevails over the definition that is incorporated herein by reference.
Referring now to the drawings,
The cell holding device 100 includes a top layer 102 having a plurality of spaced apart microwells 104 which are open on top. Each microwell 104 has a depth d and is configured to hold an individual cell. Only a single cell is loaded into each microwell 104. The microwells 104 do not pose a spatial constraint to cell morphology changes for culturing. The microwells are separated from each other.
The top layer 102 includes biocompatible material and is transparent to visible light, such as PDMS (polydimethylsiloxane), PMMA (poly (methyl methacrylate)), PC (polycarbonate), PS (polystyrene), liquid silicon rubber (LSR), and room-temperature volcanizing (RTV) silicon, for example. In some embodiments of the present invention, the thickness of the top layer 102 is between 0.5 mm and 3 mm. In some embodiments of the present invention, the microwells are set to form an array of rows parallel to each other and of columns parallel to each other. Is some embodiments of the present invention, each row is perpendicular to the columns.
In some embodiments of the present invention, the top layer 102 is joined to a substrate 106. The substrate 106 is thin material that is transparent to visible light (such as glass or polyvinylchloride, polystyrene, polycarbonate, and/or cyclic olefin copolymer (COC) that is highly compatible for microscope, for example). In some embodiments of the present invention, the thickness of the substrate 106 is between 0.1 mm and 1.5 mm. The substrate 106 provides a rigid, flat base for supporting the top layer 102. The substrate 106 provides structural strength to the chip, and therefore makes the chip 100 easier to handle and move than the more compliant top layer 102.
In some embodiments of the present invention, as shown in
The device 100 used for single cell isolation, single cell imaging, and single cell based assay applications, as the device 100 is configured to contain the single cells in culture wells during the observation and analysis.
The microwells which are in the same depression do not prevent crosstalk between the cells contained therein, as the medium in the depression is common to all cells in the microwells of the depression. Therefore, chemicals may be exchanged between cells via the medium.
On the other hand, there is atmospheric barrier between different depressions, preventing communication between cells located in different depressions. This is because the medium in one depression does not communicate with the media of other depressions. The purpose of multiple depressions is to handle multiple cell types or different media.
In some embodiments of the present invention, top layer 102 includes a plurality of spaced-apart depressions 108. Each depression 108 has a floor into which one or more microwells 104 are notched. This allows a researcher to place different kinds of cells in each depression, or place cells of the same kind in all depressions while to exposing cells in each depression to different materials. In some a non-limiting example, the depression is about 0.8 mm deep, the top layer is 1 mm deep, and each microwell has a depth of 10-20 μm. It should be noted that these sizes are merely examples, and the scope invention extends to different sizes as well.
In the example of
In some embodiments, the top layer 102 has a single depression 108 as described above with respect to the depressions 108 of
In some embodiments of the present invention, the microwells 104 in the chip have walls are shaped to increase friction between the microwell and the cell contained within. This friction decreases the movement of the cell within the microwells and therefore facilitates microinjection in the cells.
In some embodiments of the present invention, each microwell, has a top cross-section having a perimeter which includes one or more inner concave angles and one or more inner convex angles. In some embodiments of the present invention, at least one of the convex angles is an acute angle. As will be explained further below, these shapes of the top cross-section are determined by the shape of the photomask used to fabricate the chip.
In some embodiments of the present invention, the perimeter of the top cross section has a plurality of inner concave angles and inner convex angles, such that a plurality of extensions protrude inwards from the perimeter, as seen, for example in
The microwell 104 has two horizontal dimensions: a large horizontal dimension D and a small horizontal dimension M. The dimensions D and M may be perpendicular to each other and are similar to each other (e.g. within 50% of each other). Both dimensions D and M are slightly larger than a dimension of the cell, to allow the cell of be held in the microwells. A non-limiting example of a dimension D is between 10 μm and 20 μm.
The cell suspension includes a plurality of the cells that are to be captured into the microwells. The cell suspension is dropped in depression 108, so that the cells within the device 100 are captured by the microwells. In a device produced by the inventors, about 1 mm of height the depression is sufficient to hold 100 μl of the cell suspension. The same height of the depression 108 also enables low angle approach of the injection needle as explain further below and shown in
The upright microscope has a holding plate 150 with an opening 152, a light source 154, and a magnifying lens 156. A lighting system directs light from the light source 154 through the opening 152, the device 100, to the lens 154. In some examples, the microscope may be configured as an inverted microscope, in which positions of the light source 154 and the magnifying lens 156 are inversed. A microinjector 158 has a needle tip 160 that is in the viewing region of the lens 156. This enables a user to view and move the microinjector to perform a microinjection in the cell.
The shape of the device 100 enables the needle of the microinjector to be set at a low angle a respect to the device 100. In a non limiting example, the angle a may be between 15 and 45 degrees. This enables easier control of the microinjector and also enables the user to use the needle of the microinjector to push the cells against the walls of their respective microcells.
In
The structure of the chip is first plotted with computer-aided design (CAD) program and then a photomask 204 is created by printing the CAD design on glass or quartz substrate. The CAD design plotted on photomask will be transferred to photoresistor layer, as will be explained further below.
In
In
The hard-baked wafer 200 and developed photoresistor 202a serve as a mold 208, shown in
In
In some embodiments of the present invention, the liquid 212 is a 10:1 mixture of a PDMS oligomer with a crosslinking prepolymer of the PDMS agent from a Sylgard™184 kit. The mixture is placed under vacuum for degassing, and is the poured into the basin 210 of the mold 208. The mixture is cured at 80° C. for 2 hours inside the mold 208 to assume a solid form. Once solid, the mixture is peeled off from the mold. Oxygen plasma is applied to the upper layer 102 and the thin substrate 106, and then the upper layer 102 and the thin substrate 106 are bonded together. Finally, the bottomless well plate is integrated to the bonded upper layer 102.
In
This application claims priority from U.S. Provisional Application Ser. No. 62/668,606 filed May 8, 2018, which is hereby incorporated herein by reference in the respective in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62668606 | May 2018 | US |
