Patent Application
20240288765
The Sequence Listing submitted herewith is hereby incorporated by reference in its entirety. The name of the file is ILI255B_IP-2505-US_Sequence_Listing.xml, the size of the file is 16,667 bytes, and the date of creation of the file is Feb. 12, 2024.
Some available platforms for sequencing nucleic acids utilize a sequencing-by-synthesis approach. With this approach, a nascent strand is synthesized, and the addition of each monomer (e.g., nucleotide) to the growing strand is detected optically and/or electronically. Because a template strand directs synthesis of the nascent strand, one can infer the sequence of the template DNA from the series of nucleotide monomers that were added to the growing strand during the synthesis. In some examples, sequential paired-end sequencing may be used, where forward strands are sequenced and removed, and then reverse strands are constructed and sequenced. In other examples, simultaneous paired-end sequencing may be used, where forward strands and reverse strands are sequenced at the same time.
For some examples of sequential and simultaneous paired-end sequencing, one or more primer sets are attached to a polymeric hydrogel in a depression of a flow cell surface. Individual depressions are separated from one another by interstitial regions, and it is desirable for the interstitial regions to be free of both the polymeric hydrogel and the primer(s) for signal integrity. Several example methods are described herein to selectively apply the polymeric hydrogel and the primer set(s) in the depressions without applying them to the interstitial regions. These methods eliminate having to perform removal methods, such as polishing, which can lead to undesirable contamination (e.g., of the hydrogel and/or of the interstitial regions), surface alteration, and/or increasing the overall length of the manufacturing workflow.
Features of examples of the present disclosure will become apparent by reference to the following detailed description and drawings, in which like reference numerals correspond to similar, though perhaps not identical, components. For the sake of brevity, reference numerals or features having a previously described function may or may not be described in connection with other drawings in which they appear.
Examples of the flow cells disclosed herein may be used for sequencing, examples of which include sequential paired-end nucleic acid sequencing or simultaneous paired-end nucleic acid sequencing.
For sequential paired-end sequencing, a primer set is attached within a depression of a flow cell. The primers in the primer set include orthogonal cleaving (linearization) chemistry that enables forward strands to be generated, sequenced, and then removed, and then enables reverse strands to be generated sequenced and then removed. In these examples, orthogonal cleaving chemistry may be realized through different cleavage sites that are attached to the different primers in the set. Several example methods are described to generate these flow cells.
For simultaneous paired-end sequencing, different primer sets are attached to different regions within each depression of the flow cell. In these examples, the primer sets may be controlled so that the cleaving (linearization) chemistry is orthogonal in the different regions. In these examples, orthogonal cleaving chemistry may be realized through identical cleavage sites that are attached to different primers in the different sets, or through different cleavage sites that are attached to different primers in the different sets. This enables a cluster of forward strands to be generated in one region and a cluster of reverse strands to be generated in another region. In an example, the regions are directly adjacent to one another. In another example, any space between the regions is small enough that clustering can span the two regions. In any of these examples, the forward and reverse strands are spatially separate, which separates the fluorescent signals from both reads while allowing for simultaneous base calling of each read. Several example methods are described to generate these flow cells.
It is to be understood that terms used herein will take on their ordinary meaning in the relevant art unless specified otherwise. Several terms used herein and their meanings are set forth below.
The singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise.
The terms comprising, including, containing and various forms of these terms are synonymous with each other and are meant to be equally broad.
The terms top, bottom, lower, upper, on, etc. are used herein to describe the flow cell and/or the various components of the flow cell. It is to be understood that these directional terms are not meant to imply a specific orientation, but are used to designate relative orientation between components. The use of directional terms should not be interpreted to limit the examples disclosed herein to any specific orientation(s).
The terms first, second, etc. also are not meant to imply a specific orientation or order, but rather are used to distinguish one component from another.
The term “each,” when used in reference to a collection of items, is intended to identify an individual item in the collection, but does not necessarily refer to every item in the collection. Exceptions can occur if explicit disclosure or context clearly dictates otherwise.
It is to be understood that the ranges provided herein include the stated range and any value or sub-range within the stated range, as if such values or sub-ranges were explicitly recited. For example, a range of about 400 nm to about 1 μm (1000 nm), should be interpreted to include not only the explicitly recited limits of about 400 nm to about 1 μm, but also to include individual values, such as about 708 nm, about 945.5 nm, etc., and sub-ranges, such as from about 425 nm to about 825 nm, from about 550 nm to about 940 nm, etc. Furthermore, when “about” and/or “substantially” are/is utilized to describe a value, the term(s) are/is meant to encompass minor variations (up to +/−10%) from the stated value.
As used herein, the term “attached” refers to the state of two things being joined, fastened, adhered, connected or bound to each other, either directly or indirectly. For example, a nucleic acid can be attached to a functionalized polymer by a covalent or non-covalent bond. A covalent bond is characterized by the sharing of pairs of electrons between atoms. A non-covalent bond is a physical bond that does not involve the sharing of pairs of electrons and can include, for example, hydrogen bonds, ionic bonds, van der Waals forces, hydrophilic interactions and hydrophobic interactions.
As used herein, a “bonding region” refers to an area of a patterned structure that is to be bonded to another material, which may be, as examples, a lid, a substrate, etc., or combinations thereof (e.g., a substrate and a lid). The bond that is formed at the bonding region may be a chemical bond (as described above), or a mechanical bond (e.g., using a fastener, etc.).
A “patterned structure” refers to a single-layer or multi-layer substrate that includes surface chemistry in a pattern, e.g., in depressions. The surface chemistry may include a functionalized layer and primers (e.g., used for library template capture and amplification). In some examples, the substrate has been exposed to patterning techniques (e.g., etching, lithography, etc.) in order to generate the pattern for the surface chemistry. However, the term “patterned structure” is not intended to imply that such patterning techniques have to be used to generate the pattern. The patterned structure may be generated via any of the methods disclosed hereinbelow.
A “patterned resin” refers to any polymer that can have depressions defined therein. Specific examples of resins and techniques for patterning the resins will be described further hereinbelow.
The term “substrate” refers to a structure upon which various components of the flow cell (e.g., a polymeric hydrogel, primer(s), etc.) may be added. The substrate may be a wafer, a panel, a rectangular sheet, a die, or any other suitable configuration. The substrate may be inert to a chemistry that is used to modify the depressions or that is present in the depressions. For example, a substrate can be inert to chemistry used to form the polymeric hydrogel, to attach primer(s), etc. The substrate may be a single layer base support or a multi-layer structure including a base support and a layer (upon which surface chemistry is introduced) over the base support. As such, the term “base support” refers to either a single layer base support or a base support that forms a part of a multi-layer structure.
In some example methods that utilize ultraviolet (UV) light, the substrate is capable of transmitting UV light (e.g., light that is used to pattern a photoresist).
As used herein, the term “flow cell” is intended to mean a vessel having a flow channel where a reaction can be carried out, an inlet for delivering reagent(s) to the flow channel, and an outlet for removing reagent(s) from the flow channel. In some examples, the flow cell also enables the detection of the reaction that occurs in the flow cell. For example, the flow cell can include one or more transparent surfaces allowing for the optical detection of arrays, optically labeled molecules, or the like.
As used herein, a “flow channel” or “channel” may be an area defined between two bonded components, which can selectively receive a liquid sample. In some examples, the flow channel may be defined between a patterned resin of a substrate and a lid, and thus may be in fluid communication with one or more depressions defined in the patterned resin. In other examples, the flow channel may be defined between two substrates (each of which has sequencing chemistry thereon), and thus may be in fluid communication with the surface chemistry of the substrates.
As used herein, the term “depression” refers to a discrete concave feature in a substrate having a surface opening that is at least partially surrounded by interstitial region(s) of the substrate. Depressions can have any of a variety of shapes at their opening in a surface including, as examples, round, elliptical, square, polygonal, star shaped (with any number of vertices), etc. The cross-section of a depression taken orthogonally with the surface can be curved, square, polygonal, hyperbolic, conical, angular, etc. As examples, the depression can be a well or two interconnected wells. The depression may also have more complex architectures, such as ridges, step features, etc.
As used herein, the term “interstitial region” refers to an area, e.g., of a single layer or multi-layer substrate that separates depressions (concave regions). For example, an interstitial region can separate one depression of an array from another depression of the array. The two depressions that are separated from each other can be discrete, i.e., lacking physical contact with each other. In many examples, the interstitial region is continuous, whereas the depressions are discrete, for example, as is the case for a plurality of depressions defined in an otherwise continuous surface. In other examples, the interstitial regions and the depressions are discrete, for example, as is the case for a plurality of depressions in the shape of trenches, which are separated by respective interstitial regions. The separation provided by an interstitial region can be partial or full separation. Interstitial regions may have a surface material that differs from the surface material of the depressions. For example, depressions can have a functionalized polymer and one or more primer sets therein, and the interstitial regions can be free of polymer and/or primer set(s).
As used herein, the “primer” is defined as a single stranded nucleic acid sequence (e.g., single strand DNA or single strand RNA). Some primers, referred to herein as amplification primers, serve as a starting point for template amplification and cluster generation. Other primers, referred to herein as sequencing primers, serve as a starting point for DNA or RNA synthesis. The 5′ terminus of the primer may be modified to allow a coupling reaction with a functional group of a polymer. The primer length can be any number of bases long and can include a variety of non-natural nucleotides. In an example, the sequencing primer is a short strand, ranging from 10 to 60 bases, or from 20 to 40 bases.
As used herein, a “nucleotide” includes a nitrogen containing heterocyclic base, a sugar, and one or more phosphate groups. Nucleotides are monomeric units of a nucleic acid sequence. In RNA, the sugar is a ribose, and in DNA, the sugar is a deoxyribose, i.e. a sugar lacking a hydroxyl group that is present at the 2′ position in ribose. The nitrogen containing heterocyclic base (i.e., nucleobase) can be a purine base or a pyrimidine base. Purine bases include adenine (A) and guanine (G), and modified derivatives or analogs thereof. Pyrimidine bases include cytosine (C), thymine (T), and uracil (U), and modified derivatives or analogs thereof. The C-1 atom of deoxyribose is bonded to the N-1 atom of a pyrimidine or to the N-9 atom of a purine. A nucleic acid analog may have any of the phosphate backbone, the sugar, or the nucleobase altered. Examples of nucleic acid analogs include, for example, universal bases or phosphate-sugar backbone analogs, such as peptide nucleic acid (PNA).
The term “depositing,” as used herein, refers to any suitable application technique, which may be manual or automated, and, in some instances, results in modification of surface properties. Generally, depositing may be performed using vapor deposition techniques, coating techniques, grafting techniques, or the like. Some specific examples include chemical vapor deposition (CVD), spray coating (e.g., ultrasonic spray coating), spin coating, dunk or dip coating, doctor blade coating, puddle dispensing, flow through coating, aerosol printing, screen printing, microcontact printing, inkjet printing, or the like.
The term “orthogonal,” when used to describe cleaving (linearization) chemistry, means that the reagent(s) used to cleave the cleavage site of one primer in a set are not capable of cleaving the cleavage site of another primer in the same set or a different set, and vice versa. Additionally, “orthogonal” sacrificial layers are susceptible to different removal chemistries. In other words, the etch reagent used to remove one sacrificial layer will not (completely) remove another sacrificial layer due to the other sacrificial layer i) being inert to the etch reagent or ii) having a much lower etch rate when exposed to the etch reagent for another sacrificial layer.
In some examples, the term “over” may mean that one component or material is positioned directly on another component or material. When one is directly on another, the two are in contact with each other. For example, in the multi-layer substrate 15 shown in
In other examples, the term “over” may mean that one component or material is positioned indirectly on another component or material. By indirectly on, it is meant that a gap or an additional component or material may be positioned between the two components or materials. For example, in
As used herein, a “negative photoresist” refers to a light sensitive material in which a portion that is exposed to light of particular wavelength(s) becomes insoluble in a developer. In an example of the methods disclosed herein, the insoluble negative photoresist has less than 5% solubility in the developer. With the negative photoresist, the light exposure changes the chemical structure so that the exposed portions of the material becomes less soluble (than non-exposed portions) in the developer. While not soluble in the developer, the insoluble negative photoresist may be at least 99% soluble in a remover that is different from the developer. The remover may be a solvent or solvent mixture used, e.g., in a lift-off process.
In contrast to the insoluble negative photoresist, any portion of the negative photoresist that is not exposed to light is at least 95% soluble in the developer. In some examples, the portion of the negative photoresist not exposed to light is at least 98%, e.g., 99%, 99.5%, 100%, soluble in the developer.
As used herein, a “positive photoresist” refers to a light sensitive material in which a portion that is exposed to light of particular wavelength(s) becomes soluble to a developer. In these examples, any portion of the positive photoresist exposed to light is at least 95% soluble in the developer. In some examples, the portion of the positive photoresist exposed to light is at least 98%, e.g., 99%, 99.5%, 100%, soluble in the developer. With the positive photoresist, the light exposure changes the chemical structure so that the exposed portions of the material become more soluble (than non-exposed portions) in the developer.
In contrast to the soluble positive photoresist, any portion of the positive photoresist not exposed to light is insoluble (less than 5% soluble) in the developer. While not soluble in the developer, the insoluble positive photoresist may be at least 99% soluble in a remover that is different from the developer. In some examples, the insoluble positive photoresist is at least 98%, e.g., 99%, 99.5%, 100%, soluble in the remover. The remover may be a solvent or solvent mixture used in a lift-off process.
The term “transparent” refers to a material, e.g., in the form of a single layer or multi-layer substrate, that is capable of transmitting a particular wavelength or range of wavelengths. For example, the material may be transparent to wavelength(s) that are used to chemically change a positive or negative photoresist. Transparency may be quantified using transmittance, i.e., the ratio of light energy falling on a body to that transmitted through the body. The transmittance of a substrate will depend upon the thickness of the substrate, the wavelength of light, and the dosage of the light to which it is exposed. In the examples disclosed herein, the transmittance of the transparent material may range from 0.25 (25%) to 1 (100%). The material of the substrate may be a pure material, a material with some impurities, or a mixture of materials, as long as the resulting base support or substrate is capable of the desired transmittance. Additionally, depending upon the transmittance of the substrate, the time for light exposure and/or the output power of the light source may be increased or decreased to deliver a suitable dose of light energy through the substrate to achieve the desired effect (e.g., generating a soluble or insoluble photoresist).
An “acrylamide monomer” is a monomer with the structure
or a monomer including an acrylamide group with that structure. Examples of the monomer including an acrylamide group include azido acetamido pentyl acrylamide:
Other acrylamide monomers may be used.
An aldehyde, as used herein, is an organic compound containing a functional group with the structure —CHO, which includes a carbonyl center (i.e., a carbon double-bonded to oxygen) with the carbon atom also bonded to hydrogen and an R group, such as an alkyl or other side chain. The general structure of an aldehyde is:
As used herein, “alkyl” refers to a straight or branched hydrocarbon chain that is fully saturated (i.e., contains no double or triple bonds). The alkyl group may have 1 to 20 carbon atoms. Example alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl, pentyl, hexyl, and the like. As an example, the designation “C1-4 alkyl” indicates that there are one to four carbon atoms in the alkyl chain, i.e., the alkyl chain is selected from the group consisting of methyl, ethyl, propyl, iso-propyl, n-butyl, isobutyl, sec-butyl, and t-butyl.
As used herein, “alkenyl” refers to a straight or branched hydrocarbon chain containing one or more double bonds. The alkenyl group may have 2 to 20 carbon atoms. Example alkenyl groups include ethenyl, propenyl, butenyl, pentenyl, hexenyl, and the like.
As used herein, “alkyne” or “alkynyl” refers to a straight or branched hydrocarbon chain containing one or more triple bonds. The alkynyl group may have 2 to 20 carbon atoms.
As used herein, “aryl” refers to an aromatic ring or ring system (i.e., two or more fused rings that share two adjacent carbon atoms) containing only carbon in the ring backbone. When the aryl is a ring system, every ring in the system is aromatic. The aryl group may have 6 to 18 carbon atoms. Examples of aryl groups include phenyl, naphthyl, azulenyl, and anthracenyl.
An “amine” or “amino” functional group refers to an —NRaRb group, where Ra and Rb are each independently selected from hydrogen
C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C3-7 carbocyclyl, C6-10 aryl, 5-10 membered heteroaryl, and 5-10 membered heterocyclyl, as defined herein.
An “azide” or “azido” functional group refers to —N3.
As used herein, “carbocycle” means a non-aromatic cyclic ring or ring system containing only carbon atoms in the ring system backbone. When the carbocycleis a ring system, two or more rings may be joined together in a fused, bridged or spiro-connected fashion. Carbocycles may have any degree of saturation, provided that at least one ring in a ring system is not aromatic. Thus, carbocycles include cycloalkyls, cycloalkenyls, and cycloalkynyls. The carbocycle group may have 3 to 20 carbon atoms. Examples of carbocyclyl rings include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexenyl, 2,3-dihydro-indene, bicyclo[2.2.2]octanyl, adamantyl, and spiro[4.4]nonanyl.
As used herein, the term “carboxylic acid” or “carboxyl” as used herein refers to —COOH.
As used herein, “cycloalkylene” means a fully saturated carbocyclyl ring or ring system that is attached to the rest of the molecule via two points of attachment.
As used herein, “cycloalkenyl” or “cycloalkene” means a carbocyclyl ring or ring system having at least one double bond, wherein no ring in the ring system is aromatic. Examples include cyclohexenyl or cyclohexene and norbornenyl or norbornene. Also as used herein, “heterocycloalkenyl” or “heterocycloalkene” means a carbocycle ring or ring system with at least one heteroatom in ring backbone, having at least one double bond, wherein no ring in the ring system is aromatic.
As used herein, “cycloalkynyl” or “cycloalkyne” means a carbocycle ring or ring system having at least one triple bond, wherein no ring in the ring system is aromatic. An example is cyclooctyne. Another example is bicyclononyne. Also as used herein, “heterocycloalkynyl” or “heterocycloalkyne” means a carbocycle ring or ring system with at least one heteroatom in ring backbone, having at least one triple bond, wherein no ring in the ring system is aromatic.
The term “epoxy” (also referred to as a glycidyl or oxirane group) as used herein refers to
As used herein, “heteroaryl” refers to an aromatic ring or ring system (i.e., two or more fused rings that share two adjacent atoms) that contain(s) one or more heteroatoms, that is, an element other than carbon, including but not limited to, nitrogen, oxygen and sulfur, in the ring backbone. When the heteroaryl is a ring system, every ring in the system is aromatic. The heteroaryl group may have 5-18 ring members.
As used herein, “heterocycle” means a non-aromatic cyclic ring or ring system containing at least one heteroatom in the ring backbone. Heterocycles may be joined together in a fused, bridged or spiro-connected fashion. Heterocycles may have any degree of saturation provided that at least one ring in the ring system is not aromatic. In the ring system, the heteroatom(s) may be present in either a non-aromatic or aromatic ring. The heterocycle group may have 3 to 20 ring members (i.e., the number of atoms making up the ring backbone, including carbon atoms and heteroatoms). In some examples, the heteroatom(s) is/are O, N, or S.
The term “hydrazine” or “hydrazinyl” as used herein refers to a —NHNH2 group.
As used herein, the term “hydrazone” or “hydrazonyl” as used herein refers to a
group in which Ra and Rb are each independently selected from hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C3-7 carbocyclyl, C6-10 aryl, 5-10 membered heteroaryl, and 5-10 membered heterocyclyl, as defined herein.
As used herein, “hydroxy” or “hydroxyl” refers to an —OH group.
“Nitrile oxide,” as used herein, means a “RaC≡N+O−” group in which Ra is defined herein. Examples of preparing nitrile oxide include in situ generation from aldoximes by treatment with chloramide-T or through action of base on imidoyl chlorides [RC(Cl)═NOH] or from the reaction between hydroxylamine and an aldehyde.
“Nitrone,” as used herein, means a
group in which R1, R2, and R3 may be any of the Ra and Rb groups defined herein.
A “thiol” functional group refers to —SH.
As used herein, the terms “tetrazine” and “tetrazinyl” refer to a six-membered heteroaryl group comprising four nitrogen atoms. Tetrazine can be optionally substituted.
“Tetrazole,” as used herein, refers to a five-membered heterocyclic group including four nitrogen atoms. Tetrazole can be optionally substituted.
As used herein, the term “polyhedral oligomeric silsesquioxane” refers to a chemical composition that is a hybrid intermediate (e.g., RSiO1.5) between that of silica (SiO2) and silicone (R2SiO). An example of polyhedral oligomeric silsesquioxane may be that described in Kehagias et al., Microelectronic Engineering 86 (2009), pp. 776-778, which is incorporated by reference in its entirety. In an example, the composition is an organosilicon compound with the chemical formula [RSiO3/2]n, where the R groups can be the same or different. Example R groups for polyhedral oligomeric silsesquioxane include epoxy, azide/azido, a thiol, a poly(ethylene glycol), a norbornene, a tetrazine, acrylates, and/or methacrylates, or further, for example, alkyl, aryl, alkoxy, and/or haloalkyl groups.
An example of a flow cell for sequential paired-end sequencing generally comprises a patterned structure including a substrate, a functionalized layer over at least a portion of the substrate; and a primer set including two different primers attached to the functionalized layer.
An example of a flow cell for simultaneous paired-end sequencing generally comprises a patterned structure, which includes a substrate; two functionalized layers over at least a portion of the substrate; and different primer sets attached to the two functionalized layers.
One example of the flow cell 10 is shown in
Between the two patterned structures or the one patterned structure and the lid of an enclosed flow cell 10 is a flow channel 11. The two patterned structures or the one patterned structure and the lid may be bonded together via a spacer layer (not shown). Thus, in the enclosed flow cell examples, each flow channel 11 is defined by the patterned structure, the spacer layer, and either the lid or the second patterned structure.
In the open-wafer flow cell, the patterned structure may include a lane that defines a flow channel 11. Alternatively, the open-wafer flow cell may be a flat surface to which liquid reagents can be applied, and thus may not have a defined flow channel 11.
The example shown in
Each flow channel 11 is in fluid communication with an inlet and an outlet (not shown). The inlet and outlet of each flow channel 11 may be positioned at opposed ends of the flow cell 10. The inlets and outlets of the respective flow channels 11 may alternatively be positioned anywhere along the length and width of the flow channel 11 that enables desirable fluid flow.
The inlet allows fluids to be introduced into the flow channel 11, and the outlet allows fluid to be extracted from the flow channel 11. Each of the inlets and outlets is fluidly connected to a fluidic control system (including, e.g., reservoirs, pumps, valves, waste containers, and the like) which controls fluid introduction and expulsion.
The flow channel 11 may have any desirable shape. In an example, the flow channel 11 has a substantially rectangular configuration with curved ends (as shown in
The depth of the flow channel 11 (e.g., that is partially defined by layer 16 or the single layer substrate 14′) can be as small as a monolayer thick when microcontact, aerosol, or inkjet printing is used to deposit a separate (spacer) material that defines the flow channel 11 walls. For other examples, the depth of the flow channel 11 can be about 1 μm, about 10 μm, about 50 μm, about 100 μm, or more. In an example, the depth may range from about 10 μm to about 100 μm. In another example, the depth may range from about 10 μm to about 30 μm. In still another example, the depth is about 5 μm or less. It is to be understood that the depth of the flow channel 11 may be greater than, less than or between the values specified above.
The spacer layer used to attach the patterned structure and the lid or the second patterned structure may be any material that will seal portions of the patterned structure and the lid or the second patterned structure. As examples, the spacer layer may be an adhesive, a radiation-absorbing material that aids in bonding, or the like. In some examples, the spacer layer is the radiation-absorbing material, e.g., KAPTON® black (DuPont de Nemours, Inc.).
The patterned structure and the lid or the second patterned structure may be bonded using any suitable technique, such as laser bonding, diffusion bonding, anodic bonding, eutectic bonding, plasma activation bonding, glass frit bonding, or others methods known in the art.
When used, the lid may be any material that is transparent to the excitation light that is directed toward the flow cell 10. In optical detection systems, the lid may also be transparent to the emissions generated from reaction(s) taking place in the flow cell 10. As examples, the lid may include glass (e.g., borosilicate, fused silica, etc.) or a transparent polymer. A commercially available example of a suitable borosilicate glass is D 263®, available from Schott North America Inc. Commercially available examples of suitable polymer materials, namely cycloolefin polymers, are the ZEONOR® products available from Zeon Chemicals L.P. In some instances, the lid is shaped to form the top of the flow cell 10, and in other instances, the lid is shaped to form both the top of the flow cell as well as sidewalls the flow channel 11.
The patterned structure includes a bonding region where it can be sealed to the lid or to the second patterned structure. The bonding region may be located at the perimeter of each flow channel 11 and at the perimeter of the flow cell 10.
The flow channel 11 is at least partially defined by at least one patterned structure. The patterned structure may include a substrate, such as a single layer base support 14′ (as shown in
Examples of suitable single layer base supports 14′ (or base supports 14, when a multi-layer substrate 15 is used) include epoxy siloxane, glass, modified or functionalized glass, plastics (including acrylics, polystyrene and copolymers of styrene and other materials, polypropylene, polyethylene, polybutylene, polyurethanes, polytetrafluoroethylene (such as TEFLON® from Chemours), cyclic olefins/cyclo-olefin polymers (COP) (such as ZEONOR® from Zeon), polyimides, etc.), nylon (polyamides), ceramics/ceramic oxides, silica, fused silica, or silica-based materials, aluminum silicate, silicon and modified silicon (e.g., boron doped p+ silicon), silicon nitride (Si3N4), silicon oxide (SiO2), tantalum pentoxide (Ta2O5) or other tantalum oxide(s) (TaOx), hafnium oxide (HfO2), carbon, metals, inorganic glasses, resins, or the like.
In an example, the single layer base support 14′ (or the base support 14, when used as part of the multi-layer structure 15) may be a circular sheet, a panel, a wafer, a die etc. having a diameter ranging from about 2 mm to about 300 mm, e.g., from about 200 mm to about 300 mm, or may be a rectangular sheet, panel, wafer, die etc. having its largest dimension up to about 10 feet (˜3 meters). For example, a die may have a width ranging from about 0.1 mm to about 10 mm. While example dimensions have been provided, it is to be understood that a base support 14, 14′ with any suitable dimensions may be used.
As explained hereinabove, examples of the multi-layer structure 15 (when used) include the base support 14 (e.g., glass, silicon, tantalum pentoxide, or any of the other single layer base support 14′ materials) and at least one other layer 16 thereon, as shown in
In some of these examples, an inorganic oxide may be selectively applied to the base support 14 of the multi-layer structure 15 via vapor deposition, aerosol printing, or inkjet printing to form the layer 16. Examples of suitable inorganic oxides include tantalum oxide (e.g., Ta2O5), aluminum oxide (e.g., Al2O3), silicon oxide (e.g., SiO2), hafnium oxide (e.g., HfO2), etc. Other examples of the multi-layer structure 15 include the base support 14 and a patterned resin as the other layer 16. Some examples of suitable resins for the layer 16 include a polyhedral oligomeric silsesquioxane resin (e.g., commercially available under the tradename POSS® from Hybrid Plastics), a non-polyhedral oligomeric silsesquioxane epoxy resin, a poly(ethylene glycol) resin, a polyether resin (e.g., ring opened epoxies), an acrylic resin, an acrylate resin, a methacrylate resin, an amorphous fluoropolymer resin (e.g., CYTOP® from Bellex), and combinations thereof. It is to be understood that any resin material that can be selectively deposited, or deposited (on the base support 14) and patterned to form depressions 12 and interstitial regions 22, may be used for the patterned resin of the layer 16 for the multi-layer substrate 15.
Suitable deposition techniques for the layer 16 include chemical vapor deposition, dip coating, dunk coating, spin coating, spray coating, puddle dispensing, ultrasonic spray coating, doctor blade coating, aerosol printing, screen printing, microcontact printing, etc. Suitable patterning techniques for the layer 16 include photolithography, nanoimprint lithography (NIL), stamping techniques, embossing techniques, molding techniques, microetching techniques, etc. The deposition and patterning techniques that are used may depend, in part, upon the material used for the base support 14 and for the material used for the layer 16.
As shown in
Many different layouts of the depressions 12 may be envisaged, including regular, repeating, and non-regular patterns. In an example, the depressions 12 are disposed in a hexagonal grid for close packing and improved density. Other layouts may include, for example, rectilinear (rectangular) layouts, triangular layouts, and so forth. In some examples, the layout or pattern can be an x-y format in rows and columns. In some other examples, the layout or pattern can be a repeating arrangement of the depressions 12 and the interstitial regions 22. In still other examples, the layout or pattern can be a random arrangement of the depressions 12 and the interstitial regions 22.
The layout or pattern may be characterized with respect to the density (number) of the depressions 12 in a defined area. For example, the depressions 12 may be present at a density of approximately 2 million per mm2. The density may be tuned to different densities including, for example, a density of about 100 per mm2, about 1,000 per mm2, about 0.1 million per mm2, about 1 million per mm2, about 2 million per mm2, about 5 million per mm2, about 10 million per mm2, about 50 million per mm2, or more, or less. It is to be further understood that the density can be between one of the lower values and one of the upper values selected from the ranges above, or that other densities (outside of the given ranges) may be used. As examples, a high density array may be characterized as having the depressions 12 separated by less than about 100 nm, a medium density array may be characterized as having the depressions 12 separated by about 400 nm to about 1 μm, and a low density array may be characterized as having the depressions 12 separated by greater than about 1 μm.
The layout or pattern of the depressions 12 may also or alternatively be characterized in terms of the average pitch, or the spacing from the center of one depression 12 to the center of an adjacent depression 12, or from the right edge of one depression 12 to the left edge of an adjacent depression 12 (edge-to-edge spacing). The pattern can be regular, such that the coefficient of variation around the average pitch is small, or the pattern can be non-regular in which case the coefficient of variation can be relatively large. In either case, the average pitch can be, for example, about 50 nm, about 0.1 μm, about 0.5 μm, about 1 μm, about 5 μm, about 10 μm, about 100 μm, or more or less. The average pitch for a particular pattern of depressions 12 can be between one of the lower values and one of the upper values selected from the ranges above. In an example, the depressions 12 have a pitch (center-to-center spacing) of about 1.5 μm. While example average pitch values have been provided, it is to be understood that other average pitch values may be used.
The size of each depression 12 may be characterized by its volume, opening area, depth, and/or diameter or length and width. For example, the volume can range from about 1×10−3 μm3 to about 100 μm3, e.g., about 1×10−2 μm3, about 0.1 μm3, about 1 μm3, about 10 μm3, or more, or less. For another example, the opening area can range from about 1×10−3 μm2 to about 100 μm2, e.g., about 1×10−2 μm2, about 0.1 μm2, about 1 μm2, at least about 10 μm2, or more, or less. For still another example, the depth can range from about 0.1 μm to about 100 μm, e.g., about 0.5 μm, about 1 μm, about 10 μm, or more, or less. For another example, the depth can range from about 0.1 μm to about 100 μm, e.g., about 0.5 μm, about 1 μm, about 10 μm, or more, or less. For yet another example, the diameter or each of the length and the width can range from about 0.1 μm to about 100 μm, e.g., about 0.5 μm, about 1 μm, about 10 μm, or more, or less.
The depressions 12 used for sequential paired-end sequencing include a single functionalized layer 20 (as shown in
In some of the examples disclosed herein, the functionalized layers 20A, 20B (when used) are chemically the same, and any of the techniques disclosed hereinbelow may be used to sequentially immobilize the primer sets 30, 32 to the desired layer 20A, 20B. In other examples disclosed herein, the functionalized layers 20A, 20B are chemically different (e.g., the layers 20A, 20B include different functional groups for respective primer set 30, 32 attachment), and any of the techniques disclosed herein may be used to immobilize the primer sets 30, 32 to the respective layers 20A, 20B. In other examples disclosed herein, the materials applied to form the functionalized layers 20A, 20B may have the respective primer sets 30, 32 pre-grafted thereto, and thus the immobilization chemistries of the functionalized layers 20A, 20B may be the same or different.
In some examples, the functionalized layer 20 (or layers 20A, 20B, when used) may be any gel material that can swell when liquid is taken up and can contract when liquid is removed, e.g., by drying. In an example, the gel material is a polymeric hydrogel. In an example, the polymeric hydrogel includes an acrylamide copolymer, such as poly(N-(5-azidoacetamidylpentyl)acrylamide-co-acrylamide, PAZAM. PAZAM and some other forms of the acrylamide copolymer are represented by the following structure (I):
wherein:
One of ordinary skill in the art will recognize that the arrangement of the recurring “n” and “m” features in structure (I) are representative, and the monomeric subunits may be present in any order in the polymer structure (e.g., random, block, patterned, or a combination thereof).
The molecular weight of PAZAM and other forms of the acrylamide copolymer may range from about 5 kDa to about 1500 kDa or from about 10 kDa to about 1000 kDa, or may be, in a specific example, about 312 kDa.
In some examples, PAZAM and other forms of the acrylamide copolymer are linear polymers. In some other examples, PAZAM and other forms of the acrylamide copolymer are lightly cross-linked polymers.
In other examples, the gel material may be a variation of the structure (I). In one example, the acrylamide unit may be replaced with N,N-dimethylacrylamide
In this example, the acrylamide unit in structure (I) may be replaced with
where RD, RE, and RF are each H or a C1-C6 alkyl, and RG and RH are each a C1-C6 alkyl (instead of H as is the case with the acrylamide). In this example, q may be an integer in the range of 1 to 100,000. In another example, the N,N-dimethylacrylamide may be used in addition to the acrylamide unit. In this example, structure (I) may include
in addition to the recurring “n” and “m” features, where RD, RE, and RF are each H or a C1-C6 alkyl, and RG and RH are each a C1-C6 alkyl. In this example, q may be an integer in the range of 1 to 100,000.
As another example of the polymeric hydrogel, the recurring “n” feature in structure (I) may be replaced with a monomer including a heterocyclic azido group having structure (II):
wherein R1 is H or a C1-C6 alkyl; R2 is H or a C1-C6 alkyl; L is a linker including a linear chain with 2 to 20 atoms selected from the group consisting of carbon, oxygen, and nitrogen and 10 optional substituents on the carbon and any nitrogen atoms in the chain; E is a linear chain including 1 to 4 atoms selected from the group consisting of carbon, oxygen and nitrogen, and optional substituents on the carbon and any nitrogen atoms in the chain; A is an N substituted amide with an H or a C1-C4 alkyl attached to the N; and Z is a nitrogen containing heterocycle. Examples of Z include 5 to 10 carbon-containing ring members present as a single cyclic structure or a fused structure. Some specific examples of Z include pyrrolidinyl, pyridinyl, or pyrimidinyl.
As still another example, the gel material may include a recurring unit of each of structure (III) and (IV):
wherein each of R1a, R2a, R1b and R2b is independently selected from hydrogen, an optionally substituted alkyl or optionally substituted phenyl; each of R3a and R3b is independently selected from hydrogen, an optionally substituted alkyl, an optionally substituted phenyl, or an optionally substituted C7-C14 aralkyl; and each L1 and L2 is independently selected from an optionally substituted alkylene linker or an optionally substituted heteroalkylene linker.
It is to be understood that other molecules may be used to form the functionalized layers 20 or 20A, 20B as long as they are functionalized to graft oligonucleotide primer sets 30′ or 30, 32 thereto. Some examples of suitable functionalized layer materials include functionalized silanes, such as norbornene silane, azido silane, alkyne functionalized silane, amine functionalized silane, maleimide silane, or any other silane having functional groups that can attach the desired primer set. Other examples of suitable functionalized layer materials include those having a colloidal structure, such as agarose; or a polymer mesh structure, such as gelatin; or a cross-linked polymer structure, such as polyacrylamide polymers and copolymers, silane free acrylamide (SFA), or an azidolyzed version of SFA. Examples of suitable polyacrylamide polymers may be synthesized from acrylamide and an acrylic acid or an acrylic acid containing a vinyl group, or from monomers that form [2+2] photo-cycloaddition reactions. Still other examples of suitable polymeric hydrogels include mixed copolymers of acrylamides and acrylates. A variety of polymer architectures containing acrylic monomers (e.g., acrylamides, acrylates etc.) may be utilized in the examples disclosed herein, such as branched polymers, including star polymers, star-shaped or star-block polymers, dendrimers, and the like. For example, the monomers (e.g., acrylamide, acrylamide containing the catalyst, etc.) may be incorporated, either randomly or in block, into the branches (arms) of a star-shaped polymer.
The gel material of the functionalized layers 20 or 20A, 20B may be formed using any suitable copolymerization process. The gel material may also be deposited using any of the deposition methods disclosed herein.
The attachment of the functionalized layers 20 or 20A, 20B to the underlying base support 14′ (or to the layer 16 of the multi-layer substrate 15) may be through covalent bonding. In some example methods described hereinbelow, the underlying base support 14′ (or layer 16 of the multi-layer substrate 15) may first be activated, e.g., through silanization or plasma ashing, for attachment of the functionalized layer 20 or 20A, 20B. Covalent linking may be helpful for maintaining the primer set in the desired regions throughout the lifetime of the flow cell 10 during a variety of uses.
As explained previously, the depressions 12 also include the primer set 30′ attached to the functionalized layer 20, or the primer sets 30, 32 attached to respective functionalized layers 20A, 20B.
The primer set 30′ includes two different primers 31, 33 that are used in sequential paired end sequencing. As examples, the primer set 30′ may include P5 and P7 primers, P15 and P7 primers, or any combination of the PA primers, the PB primers, the PC primers, and the PD primers set forth herein. As examples, the primer set 30′ may include any two PA, PB, PC, and PD primers, or any combination of one PA primer and one PB, PC, or PD primer, or any combination of one PB primer and one PC or PD primer, or any combination of one PC primer and one PD primer.
Examples of P5 and P7 primers are used on the surface of commercial flow cells sold by Illumina Inc. for sequencing, for example, on HISEQ™, HISEQX™, MISEQ™, MISEQDX™, MINISEQ™, NEXTSEQ™, NEXTSEQDX™, NOVASEQ™, ISEQ™, GENOME ANALYZER™, and other instrument platforms. The P5 primer may be any of the following:
where “n” is inosine in SEQ. ID. NO. 2; or
where “n” is alkene-thymidine (i.e., alkene-dT) in SEQ. ID. NO. 3.
The P7 primer may be any of the following:
where “n” is 8-oxoguanine in each of SEQ. ID. NOS. 4-6.
The P15 primer is:
where “n” is allyl-T (i.e., a thymine nucleotide analog having an allyl functionality).
The other primers (PA-PD) mentioned above include:
While not shown in the example sequences for PA-PD, it is to be understood that any of these primers may include a cleavage site, such as uracil, 8-oxoguanine, allyl-T, etc. at any point in the strand.
Each of the primers disclosed herein may also include a polyT sequence at the 5′ end of the primer sequence. In some examples, the polyT region includes from 2 T bases to 20 T bases. As specific examples, the polyT region may include 3, 4, 5, 6, 7, or 10 T bases.
The 5′ end of each primer may also include a linker (e.g., 46, 46′ described in reference to
In any of the examples using the primer set 30′, the attachment of the primers 31, 33 to the functionalized layer 20 leaves a template-specific portion of the primers 31, 33 free to anneal to its cognate template and the 3′ hydroxyl group free for primer extension.
Turning now to the primer sets 30, 32, these primer sets are related in that one set includes an un-cleavable first primer and a cleavable second primer, and the other set includes a cleavable first primer and an un-cleavable second primer. The primer sets 30, 32 allow a single template strand to be amplified and clustered across both primer sets 30, 32, and also enable the generation of forward and reverse strands on adjacent functionalized layer 20A, 20B due to the cleavage groups being present on the opposite primers of the sets 30, 32. Examples of these primer sets 30, 32 will be discussed in reference to
Each of the first primer sets 30A, 30B, 30C, and 30D includes an un-cleavable first primer 34 or 34′ and a cleavable second primer 36 or 36′; and each of the second primer sets 32A, 32B, 32C, and 32D includes a cleavable first primer 38 or 38′ and an un-cleavable second primer 40 or 40′.
The un-cleavable first primer 34 or 34′ and the cleavable second primer 36 or 36′ are oligonucleotide pairs, e.g., where the un-cleavable first primer 34 or 34′ is a forward amplification primer and the cleavable second primer 36 or 36′ is a reverse amplification primer or where the cleavable second primer 36 or 36′ is the forward amplification primer and the un-cleavable first primer 34 or 34′ is the reverse amplification primer. In each example of the first primer set 30A, 30B, 30C, and 30D, the cleavable second primer 36 or 36′ includes a cleavage site 42, while the un-cleavable first primer 34 or 34′ does not include a cleavage site 42.
The cleavable first primer 38 or 38′ and the un-cleavable second primer 40 or 40′ are also oligonucleotide pairs, e.g., where the cleavable first primer 38 or 38′ is a forward amplification primer and un-cleavable second primer 40 or 40′ is a reverse amplification primer or where the un-cleavable second primer 40 or 40′ is the forward amplification primer and the cleavable first primer 38 or 38′ is the reverse amplification primer. In each example of the second primer set 32A, 32B, 32C, and 32D, the cleavable first primer 38 or 38′ includes a cleavage site 42′ or 44, while the un-cleavable second primer 40 or 40′ does not include a cleavage site 42′ or 44.
It is to be understood that the un-cleavable first primer 34 or 34′ of the first primer set 30A, 30B, 30C, and 30D and the cleavable first primer 38 or 38′ of the second primer set 32A, 32B, 32C, and 32D have the same nucleotide sequence (e.g., both are forward amplification primers), except that the cleavable first primer 38 or 38′ includes the cleavage site 42′ or 44 integrated into the nucleotide sequence (shown in
It is to be understood that when the first primers 34 and 38 or 34′ and 38′ are forward amplification primers, the second primers 36 and 40 or 36′ and 40′ are reverse primers, and vice versa.
The un-cleavable primers 34, 40 or 34′, 40′ may be any primers with a universal sequence for capture and/or amplification purposes, such as the P5 or P15 and P7 primers or any combination of the PA, PD, PC, PD primers (e.g., PA and PB or PA and PD, etc.). In some examples, the P5 and P7 primers are un-cleavable primers 34, 40 or 34′, 40′ because they do not include a cleavage site 42, 42′, 44. For example, the sequences set forth herein for P5 and P7 do not include uracil, inosine, alkene-thymidine, or 8-oxoguanine. It is to be understood that any suitable universal sequence can be used as the un-cleavable primers 34, 40 or 34′, 40′.
Examples of cleavable primers 36, 38 or 36′, 38′ include the P5 and P7 primers or other universal sequence primers (e.g., the PA, PB, PC, PD primers) with the respective cleavage sites 42, 42′, 44 incorporated into the respective nucleic acid sequences (e.g.,
Each primer set 30A and 32A or 30B and 32B or 30C and 32C or 30D and 32D is attached to a respective functionalized layer 20A, 20B. As described herein, the functionalized layer 20A, 20B may include different functional groups that can selectively react with the respective primers 34, 36 or 34′, 36′ or 38, 40 or 38′, 40′, or may include the same functional groups and the respective primers 34, 36 or 34′, 36′ or 38, 40 or 38′, 40′ may be pre-grafted or sequentially attached as described in some of the methods.
While not shown in
The PX capture primers may be:
In the example shown in
In this example, immobilization may be by single point covalent or by a strong non-covalent attachment to the respective functionalized layer 20A, 20B at the 5′ end of the respective primers 34 and 36 or 38 and 40.
Examples of terminated primers that may be used include an alkyne terminated primer, a tetrazine terminated primer, an azido terminated primer, an amino terminated primer, an epoxy or glycidyl terminated primer, a thiophosphate terminated primer, a thiol terminated primer, an aldehyde terminated primer, a hydrazine terminated primer, a phosphoramidite terminated primer, a triazolinedione terminated primer, and a biotin-terminated primer. In some specific examples, a succinimidyl (NHS) ester terminated primer may be reacted with an amine at a surface of the functionalized layer 20A, 20B, an aldehyde terminated primer may be reacted with a hydrazine at a surface of the functionalized layer 20A, 20B, or an alkyne terminated primer may be reacted with an azide at a surface of the functionalized layer 20A, 20B, or an azide terminated primer may be reacted with an alkyne or DBCO (dibenzocyclooctyne) at a surface of the functionalized layer 20A, 20B, or an amino terminated primer may be reacted with an activated carboxylate group or NHS ester at a surface of the functionalized layer 20A, 20B, or a thiol terminated primer may be reacted with an alkylating reactant (e.g., iodoacetamine or maleimide) at a surface of the functionalized layer 20A, 20B, a phosphoramidite terminated primer may be reacted with a thioether at a surface of the functionalized layer 20A, 20B, or a biotin-modified primer may be reacted with streptavidin at a surface of the functionalized layer 20A, 20B. In another example using biotin and streptavidin, streptavidin may be added to attach a biotin-modified primer and a biotinylated functionalized layer 20A, 20B.
Also, in the example shown in
In the example shown in
Examples of suitable linkers 46, 46′ may include nucleic acid linkers (e.g., 10 nucleotides or less) or non-nucleic acid linkers, such as a polyethylene glycol chain, an alkyl group or a carbon chain, an aliphatic linker with vicinal diols, a peptide linker, etc. An example of a nucleic acid linker is a polyT spacer, although other nucleotides can also be used. In one example, the spacer is a 6T to 10T spacer. The following are some examples of nucleotides including non-nucleic acid linkers (where B is the nucleobase and “oligo” is the primer):
In the example shown in
The example shown in
The example shown in
In any of the examples using the primer sets 30, 32, the attachment of the primers 34, 36 and 38, 40 or 34′, 36′ and 38′, 40′ to the functionalized layers 20A, 20B leaves a template-specific portion of the primers 34, 36 and 38, 40 or 34′, 36′ and 38′, 40′ free to anneal to its cognate template and the 3′ hydroxyl group free for primer extension.
Different methods that may be used to generate flow cells 10 are disclosed herein. The various methods will now be described.
One method of forming a flow cell 10 is depicted in
As shown in
The depression 12 may be formed in the layer 16 of the multi-layer substrate 15 using any suitable technique, such as by etching, or by nanoimprint lithography (NIL), or by photolithography, etc. When a base support 14′ (of a single layer substrate) is used, the depression 12 may be formed in the base support 14′ using any suitable technique, such as photolithography, nanoimprint lithography (NIL), stamping techniques, laser-assisted direct imprinting (LADI) embossing techniques, molding techniques, etching/microetching techniques, etc.
One example of forming the depression 12 in the layer 16 is depicted in
With the depression 12 formed in the layer 16 of the multi-layer substrate 15, this example method continues with the application of a sacrificial layer 18 over the depression 12 and over the interstitial regions 22.
Examples of suitable materials for the sacrificial layer 18 include metals (e.g., aluminum, copper, titanium, gold, silver, etc.), photoresists, and nitrides (silicon, aluminum, tantalum, etc.). Further examples of the sacrificial layer 18 include semi-metals, such as silicon and germanium. In some examples, the semi-metal or metal may be at least substantially pure (<99% pure). In other examples, molecules or compounds of the listed elements may be used, as long as they provide the desired etch stop or other function in a particular method. For example, oxides of any of the listed semi-metals (e.g., silicon dioxide) or metals (e.g., aluminum oxide) may be used, alone or in combination with the listed semi-metal or metal. As another example, silicon nitride may be used, either alone or in combination with silicon. As further examples, aluminum nitride may be used (either alone or in combination with aluminum), or tantalum nitride may be used (either alone or in combination with tantalum). These materials may be deposited using any suitable technique disclosed herein. The deposition technique used may depend, in part, upon the material used for the sacrificial layer 18. It is to be understood that in some examples of the method (e.g., when a separate photoresist is used to apply the sacrificial layer 18 at desired areas, as described in reference to
In some examples, selective deposition techniques (such as chemical vapor deposition (CVD) and variations thereof (e.g., low-pressure CVD or LPCVD)), atomic layer deposition (ALD), masking techniques, and/or etching may be used to apply the sacrificial layer 18 in the desirable areas. One of these examples involves: applying the sacrificial layer 18 over the depressions 12 and the interstitial regions 22, and etching the sacrificial layer 18 from the depressions 12, whereby the sacrificial layer 18 remains on the interstitial regions 22. This example is depicted in
As shown in
As shown in
As examples, a reactive ion etch (e.g., with 10% CF4 and 90% O2) may be used that etches the sacrificial layer 18 at a rate of about 17 nm/min. In another example, a 100% O2 plasma etch may be used that etches the sacrificial layer 18 at a rate of about 98 nm/min. Other suitable sacrificial layer 18 etchants include CF4/O2/N2, CHF3/O2, and CHF3/CO2. As still other specific examples, a CHF3 and O2 and Ar reactive ion etch may be used for a silicon dioxide sacrificial layer 18 or SF6 and O2 or CF4 and O2 or CF4 may be used for a silicon nitride sacrificial layer.
In other examples, a photoresist that is resistant to etching may be applied and developed (as described herein) prior to etching. The photoresist may be any negative or positive photoresist and may be exposed to light so that an insoluble portion of the photoresist remains over the sacrificial layer 18 at the interstitial regions 22, and so that a soluble portion of the photoresist is removed from over the sacrificial layer 18 in the depression 12. This creates a mask over the interstitial regions 22 during the etching process. In these examples, the sacrificial layer 18 within the depression 12 is removed during etching, but the sacrificial layer 18 covered by the photoresist (e.g., at the interstitial regions 22) remains intact. In these examples, etching may be performed using a dry etch process, or a wet etch process. Examples of materials and suitable wet etchants/etching conditions may include: an aluminum sacrificial layer can be removed in acidic or basic conditions, a copper sacrificial layer can be removed using FeCl3, a copper, gold or silver sacrificial layer can be removed in an iodine and iodide solution, a titanium sacrificial layer can be removed using H2O2, a silicon sacrificial layer can be removed in basic (pH) conditions, a silicon dioxide sacrificial layer can be removed using a hydrofluoric acid (HF) etch, and a silicon nitride sacrificial layer can be removed using a phosphoric acid etch.
While
Examples of suitable negative photoresists that may be used as the sacrificial layer 18 or that may be used to cover the sacrificial layer 18 (as described above) include those in the NR® series of photoresists (available from Futurrex), or in the SU-8 Series of photoresists, or in the KMPR® Series of photoresists (the two latter of which are available from Kayaku Advanced Materials, Inc.), or in the UVN™ Series of photoresists (available from DuPont). When the negative photoresist sacrificial layer 18 is used, it is selectively exposed to certain wavelengths of light to form an insoluble negative photoresist over the interstitial regions 22, and is exposed to a developer to remove soluble portions (e.g., those portions that are not exposed to the certain wavelengths of light) from the depressions 12.
Examples of suitable positive photoresists that may be used as the sacrificial layer 18 or that may be used to cover the sacrificial layer 18 (as described above) include those in the MICROPOSIT® S1800 series or the AZ® 1500 series, both of which are available from Kayaku Advanced Materials, Inc. Another example of a suitable positive photoresist is SPR™-220 (from DuPont). When a positive photoresist is used, selective exposure to certain wavelengths of light forms a soluble region (e.g., which is at least 95% soluble in a developer) in the depressions 12, and the developer is used to remove the soluble regions. Those portions of the positive photoresist overlying the interstitial regions 22 are not exposed to light, and will become insoluble in the developer. The insoluble positive photoresist thus remains over the interstitial regions 22.
The soluble portions are removed with a suitable developer so that the depressions 12 are exposed. Examples of suitable developers for the negative photoresist include aqueous-alkaline solutions, such as diluted sodium hydroxide, diluted potassium hydroxide, or an aqueous solution of the metal ion free organic TMAH (tetramethylammonium hydroxide). Examples of suitable developers for the positive photoresist include aqueous-alkaline solutions, such as diluted sodium hydroxide, diluted potassium hydroxide, or an aqueous solution of the metal ion free organic TMAH (tetramethylammonium hydroxide).
While some example methods of applying the sacrificial layer 18 to the interstitial regions 22 have been described, other examples may be used that involve photolithography and/or lift-off techniques. One of these examples, which is depicted in
As shown in
As shown in
As shown in
Following the application of the sacrificial layer 18, the insoluble photoresist 48″ (and the sacrificial layer 18 applied thereon) is then removed from the structure of
Returning now to
Any remaining portions of the sacrificial layer 18 (e.g., the portions on the interstitial regions 22) and the functionalized layer 20 that has been applied thereon are then removed via a lift-off process. This is depicted in
As shown in
While not shown, the method shown in
In other examples, the primer set 30′, including primers 31, 33, is not pre-grafted to the functionalized layer 20. In these examples, the primers 31, 33 may be grafted after the functionalized layer 20 is applied (e.g., at
When grafting is performed during the method, grafting may be accomplished using any suitable grafting techniques. As examples, grafting may be accomplished by flow through deposition (e.g., using a temporarily bound lid), dunk coating, spray coating, puddle dispensing, or by another suitable method. Each of these example techniques may utilize a primer solution or mixture, which may include the primer set 30′, water, a buffer, and a catalyst. With any of the grafting methods, the primers 31, 33 (of primer set 30′) react with reactive groups of the functionalized layer 20 and have no affinity for the layer 16 of the multi-layer substrate 15 (or the base support 14′ of the single layer substrate). As such, the interstitial regions 22 are free of the primers 31, 33.
While
Method of Forming a Flow Cell with Two Functionalized Layers Using Two Sacrificial Layers
Referring now to
While the examples of the method shown in
As shown in
The depression 12 may be formed in the layer 16 of the multi-layer substrate 15 using any suitable technique described herein, such as nanoimprint lithography (NIL) or photolithography, etc. While not shown in
With the depression 12 formed in the layer 16 of the multi-layer substrate 15, this example method continues with the application of each of the first sacrificial layer 18′ and the second sacrificial layer 26. Any example of the sacrificial layer 18 disclosed herein may be used for the first sacrificial layer 18′ and for the second sacrificial layer 26, as long the first sacrificial layer 18′ has a slower etch rate than the second sacrificial layer 26 in a particular etchant. A specific example of the sacrificial layers 18′, 26 that can be used together include aluminum (as layer 18′) and silicon nitride (as layer 26). Another example of sacrificial layers 18′, 26 that can be used together include two silicon nitride sacrificial layers 18′, 26 with different stoichiometry and different etch rates. The stoichiometry of the sacrificial layers 18′, 26 may be controlled during deposition of the sacrificial layers 18′, 26.
Different methods of depositing the first sacrificial layer 18′ and the second sacrificial layer 26 and generating the structure of
In one example, applying the first sacrificial layer 18′ over the interstitial regions 22 involves: depositing the first sacrificial layer 18′ over the substrate 15 and dry etching the first sacrificial layer 18′ from the depressions 12, whereby the first sacrificial layer 18′ remains on the interstitial regions 22. This is similar to the processes depicted in
This example continues with the application of the second sacrificial layer 26. This is depicted in
As shown in
As shown in
As shown in
Following the application of the second sacrificial layer 26, the insoluble photoresist 48″ (and the sacrificial layer 26 applied thereon) is then removed from the structure of
Another example of generating the structure of
In this example, the formation of the first sacrificial layer 18′ involves: applying a first photoresist 48 over the substrate 15 (similar to
This example method continues with the application of the second sacrificial layer 26. In this example, the formation of the second sacrificial layer 26 involves: applying a second photoresist 49 over the depressions 12 and over the first sacrificial layer 18′ (similar to
In this example method, the first photoresist 48 (used to apply the first sacrificial layer 18′) and/or the second photoresist 49 (used to apply the second sacrificial layer 26) used may be any of the negative and/or positive photoresists described herein. Any suitable developers and removers described herein may be used for the first photoresist 48 and/or the second photoresist 49.
In this example method, removal of the insoluble second photoresist 49″ and the second sacrificial layer 26 applied thereon exposes the portion 72 of the depression 12, while leaving the first sacrificial layer 18′ (remaining on the interstitial regions 22) intact. This generates the structure shown in
Following application of the first sacrificial layer 18′ and the second sacrificial layer 26 (as shown in
The second sacrificial layer 26 is then removed to expose the portion 74 of the depression 12 (e.g., the portion that had been covered by the second sacrificial layer 26). This is shown in
It is to be further understood that in these examples, the material of the first sacrificial layer 18′ is different from the material of the second sacrificial layer 26, such that the first sacrificial layer 18′ and the second sacrificial layer 26 have orthogonal wet etch chemistries. In other words, the choice of wet etch reagents is such that the reagent used for etching the sacrificial layer 26 does not etch the sacrificial layer 18′ at all, or the reagent etches the sacrificial layer 18′ at a much lower rate in comparison to the etch rate of the sacrificial layer 26. As such, at least some of the first sacrificial layer 18′ remains intact over the interstitial regions 22 after the second sacrificial layer 26 is removed. In some instances, the first sacrificial layer 18′ is not affected by the removal of the second sacrificial layer 26, and in other instances, a minimal amount of the first sacrificial layer 18′ is removed during removal of the second sacrificial layer 26. The layer 16 (e.g., in the portion 74) may function as an etch stop to second sacrificial layer 26 etching, e.g., when the layer 16 has a different etch rate than the second sacrificial layer 26 or is not susceptible to the etchant/lift-off solvent that is used to remove the second sacrificial layer 26.
As shown in
The portion 74 may first have been activated to covalently attach the second functionalized layer 20B (as described herein).
Following the application of the functionalized layer 20B, the method proceeds with the removal of the first sacrificial layer 18′ from the interstitial regions 22. This is depicted in
Removal of the first sacrificial layer 18′ (and the functionalized layer 20B thereon) exposes the interstitial regions 22 (shown in
While not shown, the method shown in
Some example methods include pre-grafting the primers 34, 36 or 34′, 36′ (not shown in
In other examples, the primers 34, 36 or 34′, 36′ are not pre-grafted to the first functionalized layer 20A. In these examples, the primers 34, 36 or 34′, 36′ may be grafted after the functionalized layer 20A is applied (e.g., at
When grafting is performed during the method, grafting may be accomplished using any suitable grafting techniques, such as those disclosed herein. With any of the grafting methods, the primers 34, 36 or 34′, 36′ react with reactive groups of the functionalized layer 20A or the primers 38, 40 or 38′, 40′ react with reactive groups of the functionalized layer 20B, and have no affinity for the layer 16 of the multi-layer substrate 15 (or the base support 14′ of the single layer substrate).
While
Method of Forming a Flow Cell with Two Functionalized Layers Using Two Different Sacrificial Layer Thicknesses
Referring now to
While the examples of the method shown in
As shown in
As shown in
Some examples of applying the sacrificial layer 18″ involve sputtering or thermally evaporating a sacrificial layer 18″ material. For example, a metal material may be sputter coated or thermally evaporated on the surface of the layer 16 of the multi-layer substrate 15. During sputtering, the metal material is deposited at an angle (e.g., 45° or 60°) relative to the surface. This creates a shadow effect in the depression 12 where less or no metal material is deposited in an area of the depression 12 that is transverse to the incoming metal material. Thus, the substrate (e.g., the base support 14′ of the single layer substrate or the multi-layer substrate 15) is rotated throughout sputtering to introduce the metal material to particular area(s) of the depression 12. As the metal material continues to be applied to the interstitial regions 22 as the substrate is rotated, this process deposits more of the metal material on the interstitial regions 22 and less of the metal material in the depression 12 due, at least in part, to the shadow effect. The pressure may also be adjusted during sputtering. Low pressure (about 5 mTorr or less) renders sputtering more directional, which maximizes the shadow effect. A similar effect may be achieved with thermal evaporation (e.g., using low pressure), and thus this technique may be used instead of sputtering to create the sacrificial layer 18″. Thus, as a result of sputtering or thermal evaporation, a sacrificial layer 18″ having a first thickness T1 is generated over a portion of the depression 12, while leaving a first portion 72′ of the depression 12 exposed, and a second thickness T2 of the sacrificial layer 18″ is generated over the interstitial regions 22 (as shown in
In other examples, photolithography and lift-off techniques are used to apply the sacrificial layer 18″ having the first thickness T1 and the second thickness T2 to generate the structure of
As shown in
As shown in
As shown in
Following the application of the sacrificial layer 18″, the insoluble photoresist 48″ (and the sacrificial layer 18″ applied thereon) is then removed from the structure of
This example continues with the application of the second photoresist 49. As shown in
As shown in
As shown in
Following the application of the additional sacrificial layer 18″, the insoluble second photoresist 49″ (and the sacrificial layer 18″ applied thereon) is then removed from the structure of
For the sacrificial layer 18″, it is to be understood that the first thickness T1 may be about 30 nm or less and is at least 10 nm thinner than the second thickness T2. In some examples, the first thickness T1 is 20 nm or less (which provides desirable UV transmittance). As such, in some instances, T1≤20≤T2−10 nm. In one example, the second thickness T2 is about 30 nm and the first thickness T1 is at least 10 nm thinner (e.g., 20 nm or less, such as 8.5 nm, 15 nm, etc.). As other examples, T1=30 nm and T2=40 nm; T1=5 nm and T2=15 nm; T1=10 nm and T2=20 nm; and T1=15 nm and T2=25 nm.
Referring back to
The entire sacrificial layer 18″ may then be exposed to a lift-off process. This process will remove the first functionalized layer 20A that is positioned on the sacrificial layer 18″, without removing the portion of the first functionalized layer 20A that is covalently attached at the second portion 72, due in part to the covalent bonding of the functionalized layer 20A to the layer 16. However, due to the differences in thickness T1 and T2, any portions of the sacrificial layer 18″ having the first thickness T1 will be completely removed (along with any functional layer 20A thereon), while any portions of the sacrificial layer 18″ having the second thickness T2 are reduced by the thickness of the first thickness T1 to form a sacrificial layer 18″ having a reduced second thickness T2′ on the interstitial regions 22 (without any functionalized layer 20A thereon). Any suitable etching process described herein may be used. This process exposes the first portion 74 of the depression 12.
In this example method, as shown at
The sacrificial layer 18″ having the reduced second thickness T2′ (and the functionalized layer 20B thereon) may be removed from the interstitial regions 22 using another lift-off process, as depicted in
Removal of the sacrificial layer 18″ having the reduced second thickness T2′ and the functionalized layer 20B thereon exposes the interstitial regions 22, as depicted in
While not shown, the method described in reference to
In other examples, the primers 34, 36 or 34′, 36′ are not pre-grafted to the functionalized layer 20A. In these examples, the primers 34, 36 or 34′, 36′ may be grafted after the functionalized layer 20A is applied (e.g., at
When grafting is performed during the method, grafting may be accomplished using any of the grafting techniques described herein.
While
To further illustrate the present disclosure, examples are given herein. It is to be understood that these examples are provided for illustrative purposes and are not to be construed as limiting the scope of the present disclosure.
One of the methods described in
SEM (scanning electron microscope) images of the flow cell surface were taken before acetone exposure (
In this example, a silanized complementary metal-oxide-semiconductor silicon substrate having a tantalum oxide layer patterned with depressions was used. Silicon nitride was used as the sacrificial layer. The silicon nitride was applied over the depressions and over the interstitial regions. A photoresist was applied over the silicon nitride at the interstitial regions. A dry etching process was performed using CF4 to remove the silicon nitride from within the depressions, while leaving the silicon nitride on the interstitial regions (e.g., the silicon nitride covered by the photoresist) intact.
PAZAM including ATTO™ 488 (VMAT2 polyclonal antibody from Alomone Labs) as a fluorescent label was used as the hydrogel, and was deposited over the silicon nitride and in the depressions. The substrate was exposed to HELLMANEX® (alkaline cleaning concentrate from Hellma) 1% at 60° C. to remove the silicon nitride and the PAZAM positioned thereon.
A confocal image of the substrate after silicon nitride removal was taken and is reproduced herein in black and white in
It should be appreciated that all combinations of the foregoing concepts and additional concepts discussed in greater detail below (provided such concepts are not mutually inconsistent) are contemplated as being part of the inventive subject matter disclosed herein. In particular, all combinations of claimed subject matter appearing at the end of this disclosure are contemplated as being part of the inventive subject matter disclosed herein. It should also be appreciated that terminology explicitly employed herein that also may appear in any disclosure incorporated by reference should be accorded a meaning most consistent with the particular concepts disclosed herein.
Reference throughout the specification to “one example”, “another example”, “an example”, and so forth, means that a particular element (e.g., feature, structure, and/or characteristic) described in connection with the example is included in at least one example described herein, and may or may not be present in other examples. In addition, it is to be understood that the described elements for any example may be combined in any suitable manner in the various examples unless the context clearly dictates otherwise.
While several examples have been described in detail, it is to be understood that the disclosed examples may be modified. Therefore, the foregoing description is to be considered non-limiting.
This application claims the benefit of U.S. Provisional Application Ser. No. 63/485,695, filed Feb. 17, 2023, the content of which is incorporated by reference herein in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 63485695 | Feb 2023 | US |
