APPARATUS, SYSTEMS AND METHODS FOR PROGRAMMABLE TISSUE CULTURE ILLUMINATION
20180016538 ยท 2018-01-18
Inventors
Cpc classification
C12M35/02
CHEMISTRY; METALLURGY
C12M31/10
CHEMISTRY; METALLURGY
International classification
C12M1/42
CHEMISTRY; METALLURGY
Abstract
The disclosed apparatus, systems and methods relate to an illumination opto-plate configured to specifically light the wells of a culture plate.
Claims
1. An illumination device, comprising: a. a base, comprising; i. a plurality of LED fixtures; ii. a microcontroller; and iii. at least one LED driver; and b. an adaptor, comprising; i. at least one layer; ii. a plurality of openings; and iii. a plurality of walls, wherein the isled fixtures are configured to illuminate a culture plate.
2. The illumination device of claim 1, wherein each of the plurality of LED fixtures is independently programmable.
3. The illumination device of claim 1, wherein the adaptor has three layers.
4. The illumination device of claim 3, wherein a plurality of diffuser paper is disposed between the adaptor layers.
5. The illumination device of claim 3, wherein the adaptor layers further comprise mounting points.
6. The illumination device of claim 3, wherein the adaptor further comprises a mounting ridge configured for reception of the culture plate.
7. The illumination device of claim 6, wherein the walls of the adaptor are configured for individual well illumination.
8. The illumination device of claim 7, wherein the opto-plate further comprises a memory.
9. A system for illuminating a culture plate comprising: a. an opto-plate, comprising: i. at least one LED fixture; ii. at least one LED driver; and iii. at least one microcontroller; b. an adaptor, comprising; i. at least one layer; ii. at least one opening; and iii. a plurality of walls, wherein the adaptor is attached to the opto-plate such that when the culture plate is placed on the adaptor the LED fixtures illuminate the culture plate.
10. The system of claim 9, wherein the walls of the adaptor are configured such that each well within the culture plate is individually illuminated.
11. The system of claim 9, further comprising a lid.
12. The system of claim 9, further comprising an Arduino configured to run independent of a computer.
13. The system of claim 12, further comprising an output port configured for linkage of multiple opto-plates.
14. The system of claim 9, further comprising a diffuser.
15. An illumination device, comprising: a. an opto-plate, comprising at least one LED fixture; and b. an adaptor, wherein the illumination device is configured to illuminate a culture plate.
16. The illumination device of claim 15, wherein the opto-plate further comprises: a. at least one LED driver; b. at least one microcontroller; c. a power jack; and d. an output port.
17. The illumination device of claim 16, wherein the opto-plate has at least one of the following features: a. a memory; b. a logic converter; c. a capacitor; and d. a resistor.
18. The illumination device of claim 17, the adaptor further comprising; a. a mounting ridge, configured to hold a culture plate; and b. a lid.
19. The illumination device of claim 15, configured to illuminate a 96 well culture plate.
20. The illumination device of claim 15, configured to illuminate a 384 well culture plate.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] The novel features are set forth with particularity in the claims that follow. A better understanding of the features and advantages will be obtained by reference to the following detailed description that sets forth illustrative embodiments and the accompanying drawings of which:
[0010]
[0011]
[0012]
[0013]
[0014]
[0015]
[0016]
[0017]
[0018]
DETAILED DESCRIPTION
[0019] The various embodiments disclosed or contemplated herein relate to devices, systems and methods for illumination of tissue culture plates. The various illumination device embodiments disclosed or contemplated herein allow independent illumination of the wells within standard cell culture plates, can be programmed to use variable timing and intensities, and can be mounted with LEDs of various wavelengths.
[0020] Turning to the drawings in greater detail,
[0021] In this implementation of
[0022] In alternate implementations, further applications known to one of skill in the art are possible. In various embodiments, the base 12 has a power jack 16 to receive electrical power from a power source 18 to power the various opto-plate components, such as the LED fixtures 20, as best shown in
[0023]
[0024] According to various implementations, llumination intensity and timing of each of the LED fixtures 20 are fully programmable and controlled through the microcontroller 34, allowing for independent illumination profiles for each well. That is, each of the various LED fixtures 20 can be illuminated independently of any of the other fixtures 20, thereby allowing for independent illumination of any one or more of the corresponding wells of the plate (not shown). It is understood that several LED fixtures 20 are referenced in
[0025] In this implementation of
[0026] It is further understood that in implementations relating to smaller numbers of wells, such as a 6-well plate, other numbers of 2-color LED 22 and/or 1-color LED 24 lights may be used in each fixture 20 because the surface area and volume of the wells of a 6- or 12-well plate are larger than the wells of a 96-well plate. For example, in certain implementations of an opto-plate 10 for a 6-well culture plate (not shown), an individual lighting fixture 20 can have ten, twelve or more total lights made up of a combination of 2-color and 1-color LEDs, as desired.
[0027] In the implementation of
[0028] Continuing with
[0029] In various implementations, the microcontroller 34 is in operable communication with the LED fixtures 20 by way of the drivers 30 and transistor 33. In certain implementations, memory 38, such as RAM, and a logic converter 40, such as a 3V-5V logic converter, can also be disposed on the base 12 and in electrical and operable communication with the microcontroller 34 and/or LED fixtures 20 and other electrical components. In certain implementations, further known components, such as capacitors and the like, can also be operationally integrated by way of further surface-mount pads 42. It is understood that additional capacitors and resistors may also be operationally integrated into the electrical components to operate various electrical functions known to those of skill in the art.
[0030] It is understood that in these implementations, the use of a plug-in microcontroller 34 can obviate the need for a data cable connection during runtime, such that the opto-plate 10 can be pre-programmed and run independent of a computer connection. Further, through use of the microcontroller 34 and other components, in certain implementations the opto-plate 10 can have additional memory 38, such as RAM, that is user-programmable and can expand the memory capacity and thus the complexity of programs run on the opto-plate 10.
[0031] Continuing with the implementation of
[0032]
[0033] Turning to
[0034] In the implementations of
[0035] In this implementation, in the middle 52 and bottom 54 layers, each opening 60B, 60C in the layers 52, 54 is surrounded by walls 62A, 62B, 64A, 64B that interlock with complementary walls on the above layer, thereby ensuring that light from one well corresponding to one opening 61 cannot spread to a neighboring well corresponding to another opening 60.
[0036] In this implementation, diffuser paper (not shown), such as two 8 mm8 mm squares of paper can be placed within the layers defining the openings 60A, 60B, 60C of each of the wells 60. In these implementations, the paper can be disposed between the layers at each well opening 60, so as to be locked into place when the layers 50, 52, 54 are locked in place. In these implementations, two layers of diffuser paper for each well opening 60 (one in the space between each adapter layer) can facilitate good diffusion of LED light, important for each cell receiving comparable amount of light. In various implementations, the layers 50, 52, 54 have mounting points 70, 72, 74, 76, 78 such that fasteners can be passed through the openings to 70, 72, 74, 76, 78 attach the layers and affix the adaptor to the base 12 at the opto-plate openings (shown in
[0037] Continuing with
[0038]
[0039] Additionally,
[0040] The implementations of
[0041]
[0042] In
[0043] Although the disclosure has been described with reference to preferred embodiments, persons skilled in the art will recognize that changes may be made in form and detail without departing from the spirit and scope of the disclosed apparatus, systems and methods.
Example
[0044] One exemplary use of the illumination opto-plate 10 is found in Cancer Mutations and Targeted Drugs Can Disrupt Dynamic Signal Encoding by the Ras/Erk Pathway. by Bugaj, L. J., Sabnis, A., Mitchell, A., Garbarino, J., Toettcher, J. E., Bivona, T. G., and Lim, W. A. and is hereby incorporated by reference in its entirety for all purposes.
[0045] For more high-throughput and long-term analysis, the optoPlate 12, a device for optogenetic illumination in microwell plates (
[0046] To test if changes in signal transmission dynamics could alter gene expression decisions in cells, the levels of several downstream output proteins in response to optoSOS inputs were measured. An experimental model was designed to isolate the effects of altered Ras/Erk kinetics in a well-controlled cell line lacking potentially confounding mutations. Thus, the responses of wild-type NIH 3T3 cells in the presence and absence of 100 M SB590885 (paradox inhibitor of B-Raf) could be compared. This concentration of drug extended Ras/Erk pathway decay kinetics while minimally elevating basal ppErk levels. Cells were seeded and starved in 384-well plates, and, in the presence or absence of drug, were exposed to various dynamic input patterns using the optoPlate 12. After stimulating the cells over several hours, cells were fixed and immunostained for Erk-dependent transcriptional targets.
[0047] For all optogenetic experiments, cells were supplemented with HPLC-purified phycocyanobilin (PCB, Frontier Scientific #P14137) at a concentration of 5 uM (3T3s) or 10 uM (all other cells). Cells were incubated in PCB for 0.5-1 hr before optogenetic stimulation. For bulk Western blot experiments, cells were illuminated in a cell culture incubator with a custom built panel of either 650 nm or 750 nm LEDs for activation or inactivation of optoSOS, respectively. For 96- and 384-well In-Cell Western and immunofluorescence experiments, optogenetic experiments were performed with a custom-built 96-well optoplate 10 with adapters 14 accommodating either 96- or 384-well plates (
[0048] The optoPlate 12 was designed to enable incubator-compatible optogenetic illumination allowing independent control of all wells in microwell plates. The optoPlate 12 is designed to independently illuminate 96 well positions corresponding to the wells of a 96-well plate. This device can also be adapted for use with 384 well plates, as each position in a standard 96-well plate corresponds exactly to 4 wells of a 384 well plate. While those 4 wells will receive the same light input, culture conditions or downstream immunostaining can be varied, expanding the parameter space for an individual experiment.
[0049] Though the optoPlate 12 is designed to illuminate up to three colors per position, in this work only two (red and far-red) were used. Illumination is driven by an Arduino Micro microcontroller 34 communicating with 12 onboard LED driver 30 chips (TLC5947). Illumination parameters are specified through a custom script written in the Arduino IDE where illumination intensity and timing can be defined for each LED 20 in each position. The wiring diagram of the circuitboard is depicted (