PROCESS FOR SELF-ASSEMBLY OF STRUCTURES IN A LIQUID

FIELD OF THE INVENTION

The present invention relates to the assembly of nucleotides to form an oligonucleotide structure and sequence determination thereof. More particularly, this present invention relates to the field of DNA sequencing.

BACKGROUND OF THE INVENTION

The art of DNA sequencing, long accomplished by a multi-step brute force approach, was radically transformed by the development of new technologies during the human genome project advancing the pace of sequencing a genome from years to months. Completion of the human genome project saw successful innovations in the fields of recombinant protein engineering, fluorescent dyes, capillary electrophoresis, automation, informatics and process management. Metzger, M. L., Genome Res, 2005; 15:1767-76).

Modern sequence analysis is most commonly directed toward discovery and analysis of sequence variation as it relates to human health and disease. These continue to be large-scale projects that are plagued by technology that is slow in its application and inaccurate in its nature. Further, current technologies available for sequence analysis tend to require large amounts of nucleic acid template and large biological samples. Important parameters which can be addressed by improved technology include increased sequencing speed, increases in sequence read length achievable during a single sequencing run, decreasing in the amount of template required to obtain positive sequence results, decreasing the amount of reagent required for processing a sequence reaction, improving the accuracy and reliability of the sequences generated, and improved identification of nucleic acid repeats in the strand of DNA.

Several unique approaches are traditionally employed for sequencing DNA. The most common is the dideoxy-termination method of Sanger (Sanger et al., PNAS USA, 1977; 74:563-567). Single nucleotide analysis such as pyro-sequencing first described by Hyman 1988 (Analytical Biochemistry, 174, pages 423-436) has proved to be the most successful non-Sanger method. Cyclic reversible termination or CRT has also been employed with some success. Finally, sequence analysis has been accomplished by an exonuclease reaction wherein particular nucleotide residues are identified in a stepwise fashion as they are removed from the end of an oligonucleotide strand.

The Sanger method represents a mixed mode process coupling synthesis of a complementary DNA template using deoxynucleotides (dNTPs) with synthesis termination by the use of fluorescently labeled dideoxynucleotides (ddNTPs). Balancing reagents between natural dNTPs and ddNTPs leads to the generation of a set of fragments terminating at each nucleotide residue within the sequence. The individual fragments are then detected following capillary electrophoresis so as to resolve the different oligonucleotide strands. The sequence is determined by identification of the fluorescent profile of each length of fragment. This method has proven to be both labor and time intensive and requires extensive pretreatment of the DNA source. Microfluidic devices for the separation of resulting fragments from Sanger sequencing has improved sample injection and even decreased separation times, hence, reducing the overall time and cost of a DNA sequencing reaction. However, the time and labor required to successfully prosecute a Sanger method is still sufficiently great to make several studies beyond the reach of many research labs.

The single nucleotide addition methodology of pyro-sequencing has been the most successful non-Sanger method developed to date. Pyro-sequencing capitalizes on a non-fluorescence technique, which measures the release of inorganic phosphate converted to visible light through a series of enzymatic reactions. This method does not depend on multiple termination events, such as in Sanger sequencing, but instead, relies on low concentration of substrate dNTPs, so as to regulate the rate of dNTP synthesis by DNA polymerase. As such, the DNA polymerase extends from the primer, but pauses when a non-complementary base is encountered until such time as a complementary dNTP is added to the sequencing reaction. This method, over time, creates a pyrogram from light generated by the enzymatic cascade, which is recorded as a series of peaks and corresponds to the order of complementary dNTPs incorporated revealing the sequence of the DNA target. (See Ronaghi, Science, 1998; 281:363-65; Ronaghi, Analytical Biochemistry, 2002; 286:282-288; Langaeet and Ronaghi, Mutational Research, 2005; 573:96-102). While pyro-sequencing has the potential of reducing sequencing time, as well as amount of template required, it is typically limited to identifying 100 bases or less. Further, repeats of greater than five nucleotides are difficult to quantitate using pyro-sequencing methods. Also, pyro-sequencing methods must be carefully designed, as it is the order of dNTP addition that determines the pyrogram profile and investigators must design experiments so as to avoid asynchronistic extensions of heterozygous sequences as almost half of all heterozygous sequences result in asynchronistic extensions at the variable site. Netzger, 2005).

Cyclic Reversible Termination (CRT) uses reversible terminating deoxynucleotides, which contain a protecting group that serves to terminate DNA synthesis. A termination nucleotide is incorporated, imaged, and then deprotected so that the polymerase reaction may incorporate the next nucleotide in the sequence. CRT has advantages over pyro-sequencing in that all four bases are present during the incorporation phase, not just a single base during a single period of time. Single base addition is achievable through homopolymer repeats and synchronistic extensions are easily maintained past heterozygous bases. Perhaps the greatest advantage of CRT is that it may be performed on many highly parallel platforms, such as high-density oglionucleotide arrays (Pease et al., 1994, and Albert et al., 2003), PTP arrays (Laymon et al., 2003), or random dispersion of single molecules (Nutra and Church, 1999). High-density arrays and incorporation of di-labeled dideoxynucleotide dNTPs by DNA polymerase gives CRT significant improvement in throughput and accuracy. However, CRT suffers several drawbacks including short read lengths that must be overcome before it can be widely employed.

Finally, exonuclease methods sequentially release fluorescently labeled bases as a second step following DNA polymerization to a fully labeled DNA molecule. Using a hydrodynamic flow detector, each dNTP analog is detected by its fluorescent wavelength as it is cleaved by the exonuclease. This method has several drawbacks. For example, the DNA polymerase and, more importantly, the exonuclease must have high activity on the modified DNA strand and generation of a DNA strand fully incorporating four different fluorescent dNTP analogs has yet to be achieved.

Technological advances in fluorescence detection are essential to decrease the amount of target oglionucleotide necessary for sequencing analysis. Four color fluorescent systems such as those employed in Sanger methods have several disadvantages including inefficient excitation of fluorescent dyes, significant spectra overlap between each of the dyes, and inefficient collection of the emission signal. Several dyes have been recently developed that help address these issues, such as fluorescence resonance energy transfer (FRET) dyes (Ju et al., PNAS, 1995; 92:4347-51; Metzger, Science, 1996: 271:1420-1422). Additional strategies have been proposed, such as fluorescence lifetime and a radio frequency modulation. Finally, Lewis et al. recently described termed pulse multiline excitation (PME) which is an ineffective method for multifluorescence discrimination. (Lewis, PNAS, 2005: 102:5346-41).

Additional operational difficulties have been observed with the existing nucleic acid sequencing methodologies, especially ones associated with sequencing by synthesis methods. By way of an example, U.S. Pat. No. 4,863,849 (patent '849) discloses a method for determining DNA sequence by sequentially adding fluorescence labeled nucleotides to a polymerization mixture. The sequencing method per patent '849 involves adding an activated nucleotide precursor (a nucleoside 5′-triphosphate) having a known nitrogenous base to a reaction mixture comprising a primed single-stranded nucleotide template to be sequenced and a template-directed polymerase. After allowing sufficient time for the reaction to occur, the reaction mixture is washed so that unincorporated precursors are removed while the primed template and polymerase are retained in the reaction mixture. The wash or effluent is assayed for the incorporation of precursors. The detection of all of the of nucleotide precursor in the effluent that is added to the reaction mixture indicates that the added precursor is not incorporated into the growing chain and, therefore, is not part of the nucleotide sequence. If less nucleotide precursor is detected in the effluent than is added, however, this indicates that the added precursor has been incorporated into the growing chain and, therefore, is the next nucleotide of the sequence. One inherent requirement, hence an inescapable obstacle, to operate the patent '849 is the entire polymerization reaction chamber has to be washed so as to deplete unincorporated nucleotides after each addition of the nucleotides. This is partly due to the fact that a dose of homogenous nucleotides is added to the polymerization reaction in an amount in excess to the corresponding nucleic acid molecules. Since a washing step is demanded after each dosing of the nucleotides, an entire sequencing process may require several thousands of washing steps. Therefore, as critical to ensure sequencing accuracy based on the signal subtraction detection as noted above, numerous washing steps per patent '849 are inherently time-consuming and laborious.

The demand for rapid small and large scale DNA sequencing has radically increased over the last several years. Current sequencing methods tend to be expensive and time consuming. Further, the prior art methods each suffer the drawback of inaccuracy in identification of repeat nucleotides in the sequence. Thus, there remains a need for a rapid and accurate sequencing method that can be run on an automated platform.

SUMMARY OF THE INVENTION

The present process relates to a process and an apparatus for nucleic acid sequencing, more specifically DNA sequencing. The inventive process is accomplished by providing a set of at least four recognition chambers. A plurality of templates is added to each chamber. Subsequently, a plurality of recognition elements is added into each chamber with each chamber receiving a homogeneous species of recognition elements that are distinguishable from the recognition elements added to each of the other chambers. The template and recognition elements are then subjected to a polymerization reaction with a plurality of polymerization enzyme so that a complementary recognition element binds and is assembled into the final structure. The process continues by identifying which of the recognition elements is complementary by method of subtraction. Finally, a plurality of building elements, each building element corresponding to the incorporated recognition element, is added to each of N chambers to complete the addition of elements at that step. This sequence is repeated until the structure is complete. By identification of each of the individual elements as it is added to the growing oligomeric structure, the sequence of the template is determined.

Recognition elements and building elements of nucleotide monomers are optionally selected from the group including nucleotides, ribonucleotides, deoxynucleotides, dideoxynucleotides, peptide nucleotides, modified nucleotides, modified peptide nucleotides, modified phosphate sugar backbone nucleotides, amino acids, or modified amino acids.

In addition to the recognition chambers, the process optionally employs a repeat detection chamber. Repeat detection achieved by small stepwise addition of less than saturated amounts of building or recognition element and detection of free element following each stepwise addition. When the element added is no longer placed in sequence, the particular site on the template is considered saturated and the number of repeat elements in the sequence is calculated.

It is further envisioned that the liquid solution from each of the recognition chambers is optionally transferred to the repeat detection chamber prior to addition of recognition or building elements. After repeat detection, the liquid reaction material is then optionally transferred from the repeat detecting chamber and divided among all N recognition chambers prior to addition of recognition elements. Optionally, all the recognition or building elements are washed out of the repeat detecting chamber or the recognition chambers prior to addition of further elements.

In an alternative embodiment, a sequence construction chamber is additionally employed where solution from the recognition chambers and the repeat detection chamber is transferred to the sequence construction chamber and the structure is increased by addition of complementary building elements. Optionally, a large sequence construction chamber is employed so that after each step of building element addition, a volume of liquid is transferred from the sequence construction chamber back to the repeat detecting chambers, as well as each of the recognition chambers. This template is then added to by new recognition elements to determine what the next element and sequence is.

It is appreciated that the oligonucleotide, or ogligomeric template, is immobilized on a support, or free in solution. It is further appreciated that recognition or building elements are optionally washed away and removed from each of the N recognition chambers, the repeat detecting chamber, or the sequence construction chamber so that a clean template can be reutilized upon each subsequent addition, hence regenerating the system. The polymerization enzyme responsible for the polymerization reaction is illustratively a DNA polymerase, an RNA polymerase, a reverse transcriptase, or mixtures thereof.

As opposed to the template being attached to a support, the polymerization enzyme is optionally attached to the support, or is itself free in solution. The nucleic acid polymerizing enzyme is optionally a thermostable polymerase or a thermodegradable polymerase. Template types operable in the instant invention include double-stranded DNA, single-stranded DNA, single-stranded DNA hairpins, RNA, and RNA hairpins. The template is optionally attached to a support by hybridizing to a primer sequence that is itself optionally affixed to a support. The primer sequence is free in solution and is complementary to a small segment of the target sequence so that a polymerization reaction may be extended from the primer.

Recognition elements optionally comprise a label or a plurality of labels. Numerous label types are operable in the instant invention illustratively including chromophores, fluorescent moieties, haptens, enzymes, antigens, dyes, phosphorescent groups, chemiluminescent moieties, scattering or fluorescent nanoparticles, FRET donor or receptor molecules, Raman signal generating moieties, precursors thereof, cleavage products thereof, and combinations thereof. In addition, photobleachable, photoquenchable, or otherwise inactivatable labels are similarly operable. The label is optionally attached to a recognition element at any suitable site illustratively including a base, a sugar moiety, an alpha phosphate, beta phosphate, gamma phosphate, or combinations thereof. It is appreciated that each homogeneous species of recognition element optionally carries a label that is distinguishable from other labels on different recognition elements.

Detection of free recognition element is accomplished by one or many of numerous identifying techniques; illustratively, far field microscopy, near field microscopy, evanescent wave or wave guided illumination, nanostructure enhancement, photon excitation, multiphoton excitation, FRET, photo conversion, spectral wavelength discrimination, fluorophore identification, background suppression, mass spectroscopy, chromatography, electrophoresis, surface plasmon resonance, enzyme reaction, fluorescence lifetime measurements, radio frequency modulation, pulsed multiline excitation, or combinations thereof.

Background fluorescence or fluorescence of previously added recognition elements to a growing structure is optionally eliminated by photobleaching the label, cleaving the label, or otherwise inactivating the label. The label is optionally cleaved from the backbone prior or subsequent to addition of recognition or building elements.

The present invention also envisions an apparatus for self-assembly of a number of elements into a structure that comprises a reaction area, a preparation area, which is in fluidic connection with said reaction area, and a detection area, which is in fluidic, physical, or optical connection with the reaction area or preparation area. It is appreciated that the reaction area has no moving parts. Within the reaction area there are at least four recognition chambers where each chamber has a plurality of microdispensers. Each microdispenser is capable of dispensing a unique species of recognition element or a building element. The chambers within the reaction area are optionally a batch flow reactor, a plug flow reactor, or a drop reactor.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is further detailed with respect to the following nonlimiting figures. These figures depict only particular processes and apparatuses according to the present invention with variants existing beyond those depicted.

FIG. 1A is a schematic of a set of reaction chambers that contain reaction chamber solution 4, template molecule 3, polymerizing enzyme 5, and all other necessary reagents wherein the open site on the template molecule 3 is depicted by a T such that only the chamber with the A recognition element 1 is subjected to a successful polymerization reaction removing the A recognition element from the solution of that chamber alone and allowing detection of free recognition element species 1 in all other chambers leading to identification of which nucleotide species is in the hybridization position;

FIG. 1B1 depicts a primer 6 affixed to a support 7, the primer 6 hybridized to a DNA template molecule wherein a polymerizing enzyme 5 recognizes the 3′ end of the template 3, and the amount of recognition element 1 added to the reaction chamber is less than that required to saturate all hybridization sites on the template strands 3;

FIG. 1B2 depicts alternative schematic immobilization of FIG. 1B1 relative to a support wherein DNA template molecule affixed to a support 7, the DNA template molecule hybridized to a primer 6 wherein a polymerizing enzyme 5 recognizes the 3′ end of the template 3, and the amount of recognition element 1 added to the reaction chamber is less than that required to saturate all hybridization sites on the template strands 3;

FIG. 1C depicts a two reaction chamber protocol wherein a biotin/streptavidin interaction immobilizes a primer 6 to a support 7 and hybridization of the template 3 to the primer immobilizes the template to the support, hence, creating a binding site for a polymerizing enzyme 5 such that a complementary recognition element depicted by a rectangle is able to hybridize with the open site on the template molecule and the polymerizing enzyme binds the complementary recognition element to the growing primer strand to form the structure, whereas the non-homologous recognition element depicted by a triangle in chamber 2 will not be added to the growing structure, furthermore, stepwise addition of the complimentary recognition element species of building element completes the repeat determination step and saturation of all template strands, washing out of all unbound elements allows a repeat of the procedure in the same reaction chambers to complete the assembly and sequence identification of the structure;

FIG. 1D depicts a schematic of chambers 1 and 2 of FIG. 1C wherein an electric potential applied throughout a detection chamber 19 is used to selectively move non-complementary elements from the reaction chamber past a detector to a collection area 18; the collected free recognition elements are optionally returned to the reaction chamber by reversing the polarity of the electric field;

FIG. 2 depicts an alternative embodiment of a reaction chamber 2 wherein recognition elements 1 are flowed over template/primer/polymerase immobilized on a support 7 mediated by a pump 16 and the presence of free recognition element 1 is determined by a detector 9;

FIG. 3 depicts an overall schematic for an apparatus of the instant invention that includes a reaction area 17 that contains reaction chambers 2 each with a plurality of microdispensers 8 that dispense elements into the reaction chamber solution 4, and the reaction chamber is in fluid connection by a fluid communication medium 12 to a repeat detecting chamber 10 and a sequence building chamber 11, the reaction area 17 is in connection with a detection area 14 and a reagent preparation area 13. In a non-limiting example where N is 4, each microdispenser 8 supplies only one homogenous type of mono nucleotide such as A, T, G or C.

FIG. 4 depicts an overall schematic for an inventive sequencing process that includes four recognition chambers 1 wherein a plurality of DNA template molecules 2 is supplied. An electrical force 6a, 6b is applied to all four recognition chambers 1 to facilitate removal of unincorporated nucleotide monomers. Each chamber 1 accepts addition of nucleotide monomers through respective micro-dispenser 3. With a DNA template molecule 2 having first three sites as T, C, G, six rounds of addition of nucleotide monomers are illustrated generally in 5 and more specifically in 5a through 5f.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention relates to a process sequencing of a deoxyribonucleotide structure into its individual monomer units. Thus, the present invention has utility as a DNA sequencing process and apparatus.

Generally, determining the sequence of a structure containing N different elements requires a system having N sets of chambers. Each of N sets in turn contains N chambers. To initiate the assembly process a different element is placed in each chamber in every set. For example the i-th chamber in every set contains the i-th element. It is appreciated that each element is optionally affixed to a wall or structure or support or to the bottom of a chamber. When the target sequence is unique, i.e. the next element is always different from the previous one, the next step in the process is to put the same element into each chamber of the same set but different elements across sets. That is, all chambers of the i-th set will receive i-th element. Since there are N sets each set containing N chambers, there are N×N possible two element strings. There will be one and only one chamber where a second element will bind to the first element to begin growing the structure. In all other chambers there will be no addition of one element to the other. Thus, by subtraction it is identified what the sequence of the first and second elements are. For example, if the growth of the structure happened in the i-th chamber of the j-th set then the first element in a sequence is the i-th and the second one is the j-th where i and j are integers greater than zero and less than or equal to N.

All sets not containing the chamber wherein a two element structure was formed are discarded such that only one set of N chambers remains. It is appreciated that all chambers are then optionally washed of free unbound elements so that the only remaining structure in the system is the surface bound or solution two element structure. At this point an excess amount of the identified element is added to each chamber of the i-th set so that all chambers contain the same two element structure.

Finding the third and every other element in the sequence is reduced to a simple algorithm. N different elements are added into N chambers to reveal the next element. All chambers are then optionally washed of the elements from all N chambers and the identified element is added to all chambers in excess to grow the structure one more unit. By repeating the steps for every member of the unidentified sequence the element order is easily determined.

In a nonlimiting example, an unidentified DNA template sequence is resolved by the instant inventive process. DNA is comprised of four element types, an adenine, guanine, thiamine, and cytosine. Therefore, the integer N is equal to 4. It is appreciated that DNA is optionally synthesized in vitro in a chamber in the presence of all required molecules illustratively including a DNA polymerase and a helicase. It is further appreciated that with a given sequence of DNA only one of the four types of elements A, T, G or C will be assembled in with the target sequence at each hybridization site being identified. It is known in the art that A hybridizes to T and G hybridizes to C. If the next element in an unknown sequence of DNA is a T only the chamber containing an A recognition element will produce extension, thus, removing the A element from solution. All other chambers will contain free nucleotide. By identifying which wells contain free nucleotide the sequence of the target is deciphered. Thus, according to the inventive process DNA sequencing is illustratively performed using four chambers with the appropriate number of DNA molecule copies in each chamber.

Of primary importance to the inventive process is that each step is conceptually split into many small steps. Each small step consists of supplying one dose of elements wherein the number of DNA template copies is much larger than the number of elements delivered during each small step. Therefore, if a particular element is incorporated into a DNA molecule at the next unoccupied site in the sequence, it is appreciated that the number of free monomers is negligible in solution after the first small step. This process allows simple identification of repeat elements (or copy number of a particular template) in the structure sequence. In a nonlimiting example the total number of DNA copies of template copies in the chamber is ten times larger than the number of elements in each single dose. It is appreciated that the first dose of elements being one-tenth that of the number of DNA will occupy sites on one-tenth of the DNA molecules leaving nine-tenths of the sites on the DNA template molecules free. After ten small additions of elements all sites on the template DNA will be occupied. Between and after each addition one-tenth concentration of element it is appreciated that there will be no free monomer elements in solution because all of the elements will be incorporated into DNA molecules. Upon addition 11 observation of free monomers in the solution occurs which signals completion of the current step and beginning of the next one. As such, a primary advantage of the instant invention over the prior art is a rapid and accurate process for revealing repeat elements or nucleotides in the sequence.

In a nonlimiting example the chamber under consideration contains 100,000 copies of DNA template molecules. One dose of monomer elements contains 10,000 molecules of monomer. Therefore, it will require 10 doses of monomer element to fill the vacancies in all copies of DNA molecules. The eleventh dose will create 10,000 monomer elements available for detection in the solution signaling that the site is not a repeat and, further, signaling the next recognition step.

During sequence identification only one chamber out of four will incorporate elements into the growing DNA structure the other three chambers will demonstrate free monomers in solution, thus, revealing the nature of the monomer which is incorporated into the growing DNA structure. After identification of which monomer element is incorporated at the particular site sufficient copies of that identified monomer element is optionally added to the other three chambers, thus, occupying that site on a growing DNA structure in all four chambers. That completes the final step of the process and determination of the entire sequence of the unknown DNA template molecule is similarly determined.

The elements supplied to the chamber are classified by purpose. The first type of element is a recognition element. Recognition elements are a plurality of homogenous nucleotide monomers optionally labeled. Recognition elements are elements identifiable as free in solution after being unable to bind in a complementary fashion to the DNA template at the next available site. The second type of element is a building element. Building elements are a plurality of homogenous nucleotide monomers which do not need to be labeled for the purpose of practicing the instant invention. The phrase of “homogenous” refers to a feature of the nucleotide monomers supplied in a dose as being of same base identity. For example, a dose of nucleotide monomers of all dATP is considered homogenous. Building elements are elements not intended to be used for recognition, however, it is appreciated that they are optionally used as recognizing elements. Building elements are designed to occupy free sites in all growing DNA structures left vacant by the non-complementary recognizing elements in a chamber.

In a non-limiting example, an inventive DNA sequencing process is depicted in FIG. 4. Four recognition chambers, namely chamber A, chamber T, chamber C, and chamber G, are employed with the chambers each respectively subject to a dosing of homogenous supply of nucleotide monomers DATP (2′-deoxyadenosine 5′-triphosphate), dCTP (2′-deoxycytidine 5′-triphosphate), dGTP (2′-deoxycytidine 5′-triphosphate), or dTTP (2′-deoxythymidine 5′-triphosphate). Within each chamber, a plurality of y number of a single-stranded DNA template molecules are provided along with a sufficient supply of polymerization enzyme and primers so as to facilitate a DNA polymerization reaction. Polymerization conditions are set forth so that a polymerization reaction within each chamber is initiated by addition of the nucleotide monomers. Nucleotide monomers are optionally activated nucleotide precursor such as a nucleoside 5′-triphosphate having a known nitrogenous base to the polymerization reaction mixture comprising a primed single-stranded DNA template molecule to be sequenced and a template-directed polymerase. The reaction conditions are adjusted to allow incorporation of the nucleotide precursor only if it is complementary to the single-stranded DNA template molecule at the site located one nucleotide residue beyond the 3′ terminus of the primer. The plurality of DNA template molecules are each optionally immobilized on a support within each chamber. To each chamber, a dose of respective homogenous nucleotides is added whereas the dose corresponds to x number of nucleotide monomers, such as x number of dATP, dCTP, dTTP, or dGTP molecules. It is appreciated that x is a number less than half the number y. A theoretical number of x is one and hence of y is two. Suppose the next in position in the DNA sequence is a “T”, there is an immediate match in chamber A whereas a first dose of x number of dATP monomers are present. Because x is less than half the number of DNA template molecules, all x number of dATP monomers are matched and incorporated to the DNA template molecules leaving no free dATP monomers in Chamber A. Concurrently in chambers T, C, or G, since no nucleotide matching exists between the “T” position in the DNA template molecules and dCTP, dGTP, or dTTP, all these added nucleotide monomers are never incorporated and remain free in their respective chambers T, C. G. A suitable detection method is employed to monitor occurrence of unincorporated nucleotide monomers present in each chamber or present optionally in an effluent when contents in that chamber are at least partially contained in a solution. In so doing, nucleotide monomers are labeled with fluorescence and the detection method is a fluorescent imager. For the purpose of DNA sequencing, upon first dosing of nucleotide monomers in each of the four chambers, the nucleotide identity of the next in position in DNA template sequence is determined by the lacking of immediate fluorescence reading present in the effluent. Then an equivalent amount of nucleotide monomers (building elements of nucleotide monomers) of that same identify is supplied to the other three chambers where immediate fluorescence reading is observed, namely chamber T, C, G in the present example. The purpose of adding the building elements of nucleotide monomers is to occupy the “T”s in the DNA template molecules after first round of recognition and to expose the nucleotide positions downstream of the “T”. This process is repeated till the entire sequence of the DNA template is determined. The movement of nucleotide monomers within their respective chambers is optionally facilitated through an electric force; however, it is noted that the electric force is not deemed to interfere with the polymerization reaction. Therefore it is appreciated that once a matching of nucleotides occurs between the DNA template and an added nucleotide monomer, the electric force is applied so as not to cause to break the matching bond or even to interfere with the matching process. The fluorescence detection is a “presence”/“absence” event meaning the presence of fluorescence reading associated with the presence of very first unincorporated nucleotide molecule is all that is needed to make a determination as to the identify of the nucleotide sequence in that position. This is advantageous over the prior art method where, such that in the patent '849, a laborious fluorescence signal subtraction method is mandated. The electric force is applied either in pulses or continuously. When the electric force is applied in a pulsatile fashion, the electric force must be applied after each step of recognition and after each step of building. Nucleotide monomers in the effluent after the application of the electric force is optionally collected and reused for the sequencing process.

The “size” of a dose of recognition elements of nucleotide monomers is the total number of homogenous nucleotide molecules included in the dose. The size of each dose of nucleotides is preferably less than half the total copy number of DNA molecules in a sample. A theoretically possible minimum of the size of a dose of nucleotides is one; therefore a theoretically possible minimum of the total copy number of DNA molecules is two.

The inventive process is operable for many different types of sequence structures or element containing structures. A recognition element or a building element is illustratively a nucleotide, a ribonucleotide, deoxyribonucleotide, deoxynucleotide, peptide nucleotides, modified nucleotides, modified peptide nucleotides, modified phosphate sugar backbone nucleotides, amino acids, or modified amino acids.

Recognition elements are optionally labeled. A single label or multiple labels are optionally present on each individual recognition element. In a nonlimiting example, during DNA sequencing four different types of recognition elements are employed: A, T, G, or C. Each recognition element optionally contains the same label or different labels that are distinguishable from each other based on characteristics of the combination of label and the remainder of the recognition element. Labels are optionally bound to one or multiple sites on a recognition element such as in a nucleotide. Recognition elements optionally have a label attached at a base, on a sugar moiety, on the alpha phosphate, beta phosphate, gamma phosphate, or any combination thereof. Illustratively, a label for adenine preferably has a fluorophore bound to the gamma phosphate wherein the fluorophore is distinguishable from a fluorophore bound to the gamma phosphate on a different species of recognition element. Thus, in the case of DNA sequence the four recognition element species optionally contain four different fluorophores.

Multiple label types are operable in the instant invention illustratively including chromophores, fluorescent moieties, enzymes, antigens, dyes, phosphorescent groups, chemiluminescent moieties, scattering or fluorescent nanoparticles, Raman signal generating moieties, fluorescence resonance energy transfer donor or acceptor molecules, precursors thereof, cleavage products thereof, and combinations thereof. In addition, it is appreciated that the label on any recognition element is optionally photo bleachable, photo quenchable, or inactivatable. A recognition element is optionally bound into a single strand of growing DNA in the formation of a structure, and prior to, during, or subsequent to the addition of this recognition element the label is photo bleached such that contamination of the fluorescence of the label does not interfere with subsequent identification steps.

Identifying the presence or absence of free recognition elements in a chamber is dependent on the type of label present on the individual recognition elements. Numerous identifying methods are known in the art illustratively including far field microscopy, near field microscopy, evanescent wave or wave guided illumination, nanostructure enhancement, mass spectroscopy, photon excitation, multi photon excitation, FRET, photo conversion, spectral wavelength discrimination, fluorophore identification, background suppression, electrophoresis, surface plasma in resonance, enzyme reaction, fluorescence lifetime determination, radio frequency modulation, pulsed mutiline excitation, or combinations thereof.

It is appreciated that the structures are optionally complementary to a DNA template structure that guides which element is placed in the next location in the sequence. Illustratively, the template structure is a DNA oligonucleotide sequence. Template DNA sequences are optionally free in solution or bound to a support in a recognition chamber or to the recognition chamber wall itself. Immobilization of the template is accomplished through conventional techniques known in the art illustratively including covalent attachment to a functional group on the solid surface, or by biotin/avidin interaction. In an optional embodiment a short oligonucleotide primer is bound to a support. The oligonucleotide segment is complementary to a small known sequence on the DNA template strand. Hybridization of the DNA template strand with the surface bound oligonucleotide immobilizes the DNA template to the surface of the chamber in reversible fashion. This embodiment has the additional advantage of providing a primer sequence for a polymerization reaction to occur. It is common in the art of DNA sequencing analyses that small segments of known sequence are present at the termination of each unknown strand. The template strand is optionally double stranded DNA, single stranded DNA, single stranded DNA hairpins, RNA, or RNA hairpins.

The inventive process further comprises a polymerization reaction in which one unknown recognition element or building element is added to the growing DNA structure in a complementary fashion. The polymerization reaction is performed by a nucleic acid polymerizing enzyme that is illustratively a DNA polymerase, RNA polymerase, reverse transcriptase, or mixtures thereof. It is further appreciated that accessory proteins or molecules are present to form the replication machinery. In a preferred embodiment the polymerizing enzyme is a thermostable polymerase or thermodegradable polymerase. Use of thermostable polymerases is well known in the art such as Taq polymerase available from Invitrogen Corporation. Thermostable polymerases allow a recognition or building reaction to be initiated or shut down by a change in temperature or other condition in the chamber without destroying activity of the polymerase.

Accuracy of the base pairing in the preferred embodiment of DNA sequencing is provided by the specificity of the enzyme. Error rates for Taq polymerase tend to be false base incorporation of 10⁻⁵or less. Johnson, Annual of Biochemistry, 1993: 62:685-713; Kunkel, Journal of Biological Chemistry, 1992; 267:18251-18254 (both of which are hereby incorporated by reference). Specific examples of thermostable polymerases illustratively include those isolated from Thermus aquaticus, Thermus thermophilus, Pyrococcus woesei, Pyrococcus furiosus, Thermococcus litoralis and Thermotoga maritima. Thermodegradable polymerases illustratively include E. coli DNA polymerase, the Klenow fragment of E. coli DNA polymerase, T4 DNA polymerase, T7 DNA polymerase and other examples known in the art. It is recognized in the art that other polymerizing enzymes are similarly suitable illustratively including E. coli, T7, T3, SP6 RNA polymerases and AMV, M-MLV, and HIV reverse transcriptases.

The polymerases are optionally bound to a primer template sequence. When the template sequence is a single-stranded DNA molecule the polymerase is bound at the primed end of the single-stranded nucleic acid at an origin of replication or with double stranded DNA to a nick or gap. Similarly, secondary structures such as in a DNA hairpin or an RNA hairpin allow priming to occur and replication to begin. A binding site for a suitable polymerase is optionally created by an accessory protein or by any primed single-stranded nucleic acid.

In a preferred embodiment the template is bound to a support located within a recognition chamber. Materials suitable for forming a support optionally include glass, glass with surface modifications, silicon, metals, semiconductors, high refractive index dielectrics, crystals, gels and polymers. A support is illustratively a planar or spherical surface. It is appreciated in the inventive process that either a sequencing primer in the case of DNA sequencing, a target nucleic acid molecule, or the nucleic acid polymerizing enzyme are illustratively immobilized on the support. A complementary bonding partner for forming interactions with any of the above molecules or any other of the operational machinery in the inventive process are similarly appreciated to be suitable for immobilizing material onto a surface. Interaction of any of the replication machinery with the surface is optionally nonspecific. Examples of a specific type bonding interaction include a biotin/streptavidin linkage wherein a known primer sequence is optionally labeled with a biotin and the solid support is labeled with a streptavidin. When the biotin primer is added to the chamber a tight bonding interaction between the biotin and streptavidin occurs immobilizing the primer sequence onto the support surface. It is further appreciated that the target DNA sequence is optionally labeled itself so that it is immobilized on the support surface. Additionally, a primer sequence is optionally immobilized by hybridization with a complementary immobilized oligonucleotide. Thus a primary oligonucleotide is immobilized on a surface with a short sequence complementary to the primer oligonucleotide. It is preferred that the primer oligonucleotide is of sufficient additional length that hybridization between the immobilized nucleotide and the primer oligonucleotide allows base pairing between the primer oligonucleotide and the target DNA sequence, thus, binding the target DNA sequence to the support surface. Interaction of any suitable molecule to the support surface is appreciated to be reversible or irreversible. Alternative exemplary methods for immobilizing sequencing primer or target nucleic acid molecule to a support include antibody antigen binding pairs or photoactivated coupling molecules. It is appreciated in the art that numerous other immobilizing methods are similarly suitable in the inventive process.

It is further appreciated that the proteinaceous material of the polymerization enzyme in the case of a DNA polymerase is optionally immobilized on the surface either reversibly or irreversibly. For example, RNA polymerase was successfully immobilized on activated surface without loss of catalytic activity. Yin et al., Science, 1995; 270: 1653-57, which is hereby incorporated by reference. Alternatively, an antibody antigen pair is utilized to bind a polymerase enzyme to a support surface whereby the support surface is coated with an antibody that recognizes an epitope on the protein antigen. When the antigen is introduced into the reaction chamber it is reversibly bound to the antibody and immobilized on the support surface. A lack of interference with catalytic activity in such a method has been reported for 1 reverse transcriptase. Lennerstrand, Analytical Biochemistry, 1996; 235:141-152, which is hereby incorporated by reference. Additionally, DNA polymerase immobilization has been reported as a functional immobilization method in Korlach et al., U.S. Pat. No. 7,033,764 B2; incorporated herein by reference. Finally, any protein component can be biotinylated such that a biotin streptavidin interaction is optionally created between the support surface and the target immobilized antigen.

In a preferred embodiment both the DNA template molecule and the polymerase remain free in solution. Referring to FIG. 1, the sequencing procedure is initiated in a solution optionally containing the DNA template 3 as well as one of N species of recognition elements 1. Illustratively, four recognition element species are available represented by A, T, G and C. The four recognition chambers correspond to each species of recognition element wherein an individual species of recognition element is added. In each chamber a reaction is optionally initiated by the addition of a nucleic acid polymerizing enzyme. In an alternative embodiment a primed target sequence may be established by pre-addition of a target sequence, a primer, and a species of recognition element. No structure extension occurs in the absence of a DNA polymerase. The reaction is initiated by addition of the DNA polymerase. In an alternative embodiment all components of the replication machinery are present including the DNA polymerase, the template molecule, the primer, and a particular recognition element. The solution in this embodiment is optionally void of necessary ions for the function of the polymerase enzyme. For example, the reaction may be initiated by the addition of magnesium ions such that the replication machinery now becomes functional. In yet another alternative embodiment all of the reaction machinery is present, however, the reaction chamber is heated above a threshold temperature above the melting temperature of the template molecule and the primer such that hybridization between the primer and the template molecule does not occur. The polymerization reaction begins by adjusting the temperature to a suitable reaction temperature.

In the preferred embodiment depicted in FIG. 1A recognition element species are added to each chamber to initiate a polymerization reaction. Recognition elements are thereby diffused through the fluid medium or forced to flow through the chamber via hydrodynamic pump rapidly bringing the recognition element into association with the polymerization machinery. A recognition element inserts into the active site of the polymerase and the polymerase establishes whether this nucleotide analog is complementary to the first open base of the target nucleic acid molecule or whether a mismatch has occurred. In the reaction chamber illustrated in FIG. 1A where an A recognition element is added to the reaction chamber it is appreciated that the template at the next recognition site is defined by a T. Should an A recognition element be incorporated into the polymerase a positive match will occur and the polymerization machinery will form a covalent bond between the A and the primer sequence. However, in the second tube where a T recognition element is added a mismatch occurs and no polymerization process will proceed. If the ratio between the recognition element and the template is proper such that the recognition element illustratively is one-tenth the concentration of the template it is appreciated that all of recognition element in the A chamber will be bound and polymerized at the first hybridization site on the template molecule.

Each chamber is optionally in fluidic connection with a detector such that by removing each of the chambers free recognition elements are transported to the detector area and are readily detected. In a preferred embodiment each of the recognition elements is differentially labeled such that it can be easily distinguished from other recognition elements. Thus, a single detector is employed whereby the individual unincorporated element species are readily identified, thus, determining the sequence at the first hybridization site in the template molecule.

As depicted in FIG. 1D, an electrophoretic gel such as that formed by acrylamide, agarose, or other material known in the art is used intermediate each reaction chamber and a dedicated collection area 18 with a detector intermediate therebetween. Following sufficient time for all recognition elements to hybridize with the template strand, an electric potential is applied moving the free nucleotides past a detector 9 to the collection area. After identification of the next element in sequence, all unused elements are optionally returned to their respective recognition chambers by reversing the polarity of the electric field. This embodiment of the invention has the advantages of reducing reagent costs and time between sequencing iterations while simultaneously providing a reversible washing step for improved sequence addition.

In an alternative embodiment a sampling of each of the reaction chambers is obtained and injected into a mass spectrometer to recognize the presence of free elements. This embodiment has the advantage of using native, non-labeled elements whereby greater efficiency and accuracy of the polymerase is achieved. Alternatively, it is appreciated that multiple detector types are optionally employed. In a nonlimiting example, the recognition elements are fluorescently labeled. Detection of the species of hybridizing recognition element is, thus, detected by a fluorometer.

In a preferred embodiment the template is bound to a support. Unincorporated recognition elements of nucleotide monomers are optionally removed from recognition chambers. In an alternative embodiment the fluidic connection between each reaction chamber in the detector is such that the large template molecule remains in the chamber while the small recognition elements are readily transported through a barrier such as a size exclusion membrane or an electrophoretic gel. As such, each chamber is washed free of unbound recognition elements.

After identification of the particular recognition element species bound to the template molecule, building elements are added to each of the chambers at a known concentration to fully saturate all DNA template molecules. At this point all unbound recognition element and building element species are optionally removed from each chamber and the reaction cycle begins again so as to determine the next recognition element species in each of the template strands. Thus, by repeating the sequence of steps the sequencing primer is extended and the entire sequence of the target is determined.

The polymerization reaction is optionally conducted in a solution. It is appreciated that the solution be of suitable extension medium so as to permit diffusion, incorporation, and washing out of each of the reaction chambers. In a nonlimiting example suitable extension media a contains 50 mM Tris-HCl pH 8.0, 25 mM magnesium chloride, 65 mM sodium chloride, 3 mM DTT, and elements at appropriate concentration to permit identification of the sequence. It is appreciated that other extension medium are similarly suitable and optimized for the particular polymerase or template being utilized.

In an alternative embodiment as in the present nonlimiting illustration, a fifth chamber is present termed a repeat detecting chamber wherein, following identification of the recognition element species, recognition element species is added to the repeat detecting chamber to determine whether or not a repeat exists and the number of repeats in sequence. Following identification of both the recognition element species in the original reaction chambers as well as the number of repeats in the repeat detecting chamber, a suitable concentration of building elements is added to all chambers to fully saturate all sites at that portion in the growing structure. It is appreciated that a washing out procedure is optionally employed between each subsequent sequence whereby the unbound elements in all reaction chambers are removed.

In an alternative embodiment the repeat detecting chamber is in fluidic communication with each of the four reaction chambers. All the reaction solution from each of the four reaction chambers is transferred to the repeat detecting chamber. It is in the repeat detecting chamber that stepwise addition of the identified species of recognition element is added to determine whether or not a repeat exists. Once the presence of a repeat is determined, or shown not to exist, the repeat detecting chamber is optionally washed free of all unbound recognition elements and the fully hybridized growing DNA molecule is subsequently transferred back to each of the four reaction chambers for the next round of element recognition.

In an alternative embodiment there is no washing out of the elements which are left in solution as excessive free elements after each of the previous steps. However, it is appreciated that the ratio between recognition elements and template is such that there is little to no observable contamination as the procedure moves through several rounds of recognition. For example, in a situation with five chambers, four recognition chambers and a repeat detecting chamber, four contain copies of free DNA molecules to be sequenced. Each chamber is initially supplied only with a small dose of one species of recognition element. This small dose is illustratively one-tenth concentration of target DNA molecules to be sequenced. After identification of the next hybridizing recognition element that element is added to the fifth chamber only using small doses to determine if there is a repeat. After the correct dose of that element is determined, the appropriate concentration of building element is added to the first four chambers and the next round of recognition begins.

In an alternative embodiment there is no removal of unincorporated recognition elements or building elements after each of the previous steps. However, it is appreciated that the ratio between recognition elements and DNA template molecules is such that there is little to no observable contamination as the procedure moves through several rounds of recognition. For example, in a situation with four recognition chambers each containing copies of free DNA molecules to be sequenced. Each chamber is initially supplied only with a small dose of one species of recognition elements. This small dose is illustratively one-tenth concentration of DNA template molecules to be sequenced. If the number of doses required for detecting the presence of free monomers in solution is smaller than the number of doses required to saturate all the copies of DNA template, there is no need to wash free non-incorporated monomers out.

In yet another alternative embodiment a fifth chamber is present termed a sequence construction chamber Four recognition chambers contain copies of free DNA molecules to be sequenced, and each chamber is supplied with only a single species of recognition element. Subsequently, the solution from all four chambers is then moved to a fifth chamber where the appropriate number of building elements for all four chambers is added to the resulting solution so as to fully saturate all free sites in the growing structure that are complementary to the current hybridization site on the template. Following saturation of all sites the solution from the sequence construction chamber is transferred back equally to each of the four recognition chambers. All chambers now contain a DNA template molecule hybridized to a growing structure of equal length and a new round of recognition element species identification occurs.

In an alternative embodiment, after one round of recognition process, entire content of polymerization reaction mixture of each recognition chamber is removed and discarded. Sufficient building elements of same nucleotide identified in this round of recognition process are added to a sequence construction chamber where DNA template molecules in an amount four times of the DNA template molecules in each of the recognition chambers so as to fully saturate all hybridization sites on the template DNA molecule in this chamber. Unincorporated building elements are then removed and the residual contents of the sequencing construction chamber are divided equally and added back to each recognition chamber, and from there a new round of recognition process awaits to begin.

In an alternative process employing five chambers, four recognition chambers and one large sequence construction chamber, four small volumes of target DNA molecules in solution, or immobilized on a support in suspension, are transferred from the sequence construction chamber to each of the four recognition chambers. The next element in sequence is determined as described above. After the recognition element species is identified, the solution from all four recognition chambers is transferred back to the sequencing construction chamber where building elements are added to complete saturation of the identified vacancies on the growing DNA template molecules. It is appreciated that in this embodiment simultaneous sequencing of target DNA occurs. For example, in the situation where one large sequencing construction chamber is utilized small samples are withdrawn and divided amongst the four recognition chambers. The next element in series is identified and the presence of repeats is determined. The proper dose of building elements is then added to the sequence construction chamber to fully saturate all sites on the growing DNA structure.

It is appreciated that numerous other embodiments of the instant invention exist with greater or fewer chamber numbers, types, sizes, interconnections, or pathways and are also the subject of the instant invention.

An embodiment of the instant invention includes an apparatus. This apparatus optionally employs numerous reactor types illustratively including a batch reactor, a plug flow reactor, or a drop reactor. An apparatus for self-assembly of a number of elements comprises a reaction area that contains a suitable number of chambers relative to the number of different species of elements in the growing structure; a preparation area in fluidic connection with the reaction area whereby reagents and solutions are prepared to be delivered to the reaction area in stepwise or simultaneous fashion; and a detection area in fluidic, physical, or optical connection with the reaction area.

The detection area employs any suitable detector for detection of the type of label on each of the individual recognition elements. For example, if each of the recognition elements is labeled with a particular fluorophore a fluorescent detector is employed so as to identify which chambers contain free recognition elements. In the case where either unlabeled recognition elements are employed or nonoptically resolvable recognition elements are employed each of the reaction chambers is optionally connected to a mass spectrometer whereby the presence of free recognition elements is readily determined.

In the inventive apparatus the reaction area has N recognition chambers, each chamber having a plurality of microdispensers. The number of microdispensers is related to the number of possible recognition element species. For example, if there are four recognition element species each chamber in the reaction area has four microdispensers to allow distribution of the various species of recognition element. In an alternative embodiment there are eight microdispensers aimed at each of the reaction chambers such that any of the four recognition elements are optionally distributed to each reaction chamber as well as any building elements without fear of contamination between the elements. Thus, each microdispenser is filled with one type of element so that each type of element is available to be distributed into each chamber in the reaction area. In the case of five small chambers the fifth chamber similarly has four or eight microdispensers for delivery of elements to that chamber. It is appreciated that the number of microdispensers is optionally related to the number of the elements in the growing structure. In the case of ten separate element species as many as ten or twenty microdispensers for each chamber are employed. Alternatively, a single or fewer than N microdispensers is employed with a washing out step of each of the microdispensers between delivery of different recognition or building elements.

It is appreciated that the reaction area contains no moving parts. Fluidic connection between each of the chambers is optionally powered by differential electric potential so as to move free recognition or building elements between the chambers. Further, DNA template and growing structure may similarly be transferred between chambers.

Example 1

A standard reaction chamber protocol is outlined in FIG. 1C. DNA template with a known termination sequence of 3′-CAT TTT GCT GCC GGT CA- . . . -5′ (SEQ ID No. 1) is amplified by standard PCR techniques and purified on an anion exchange resin supplied by Quiagen, Inc., Valencia, Calif. 400 ng of template is added to each of four reaction chambers, a repeat detection chamber, and a sequence building chamber each containing a reaction solution of 60 mM Tris-SO₄(pH 8.9), 180 mM Ammonium Sulfate. A primer (8 μg) of complementary sequence 5′-GTA AAA CGA CGG CCA GT-3′ (SEQ ID No. 2) is added to each chamber and allowed to hybridize with the DNA template under suitable conditions. A single species of Fluorecein-12 labeled A, T, G, and C nucleotides obtained from Perkin Elmer, Waltham, Mass. are added to each of the four reaction chambers 1/10 mol/mol concentration relative to DNA template. A polymerization reaction is initiated by the addition of 1 unit (final) of Platinum® Taq DNA Polymerase (Invitrogen, Inc., Carlsbad, Calif.) along with 2 mM MgSO₄(final) in reaction solution. The reaction is allowed to proceed for 5 sec. An electric potential is applied to the solution of each reaction chamber in sequence whereby free nucleotide is selectively moved from the reaction chamber toward a detection area in which a fluorescent detector determines whether a fluorescent nucleotide is present in solution. Fluorescent parameters are 496 nm excitation, 517 nm emission with a 5 nm bandpass filter. Identification of which reaction chamber does not possess free labeled recognition element determines which element is next in sequence. The reaction chamber in which a labeled A was added demonstrates no free nucleotide.

Fluorescein-12 labeled A is added to the repeat detection chamber along with DNA polymerase, MgSO₄₁and reaction solution by a microdispenser in 1/10 mol/mol amounts in sequential fashion and the reaction is allowed to proceed for 5 seq followed by application of an electric potential to determine if free nucleotide is present in solution. It is appreciated that other relative amounts of nucleotide and template are similarly suitable in all chambers. Application of an electric potential moves free nucleotide to a detector area where the presence of free nucleotide is determined as above. The process in the repeat detection chamber is repeated until free nucleotide recognized by the detector. Twenty additions are required for the instant exemplary template strand indicating that there is an AA repeat sequence.

2× mol/mol concentration of unlabeled A nucleotide (building element) is added to each of the reaction chambers and the sequence building chamber and the polymerization is allowed to proceed for 2 min followed by application of an electric potential to wash out any remaining free recognition or building element from all chambers.

The process is repeated for 350 cycles to fully assemble and identify the sequence of all nucleotide elements in the DNA sequence.

Example 2

Referring to FIG. 2, a reaction chamber 2 is depicted as illustrated by a tubular loop structure wherein a support 7 is coated on a portion thereof which contains reaction solution. The support is coated with streptavidin by techniques known in the art. The primer of Example 1 is biotinylated by techniques known in the art illustratively by incorporation of biotin-aha-CTP (Invitrogen) in the primer sequence at the 5′ end. The primer is added to the reaction chamber and allowed to interact with the support. DNA template is then added at a concentration such that nearly all the DNA template will be hybridized with primer. Recognition elements 1, polymerase 5, and initiation ions such as in Example 1 are added by a microdispenser to the reaction chamber and a pump 16 circulates the fluid in the chamber such that the recognition element is flowed across the template bound support for 10 seconds with continuous monitoring by the fluorescent detector 9. Over the course of the reaction time the reaction chamber that contains the complementary recognition element demonstrates a reduction in fluorescence indicating that the element is incorporated onto the support bound primer. Analyses of each respective reaction chamber identify the next nucleotide in sequence. Two other similar reaction chambers, or standard container chambers are employed for the repeat detection chamber and the sequence building chamber and the structure building reaction and sequence identification is completed by subsequent iterative steps.

Patent documents and publications mentioned in the specification are indicative of the levels of those skilled in the art to which the invention pertains. These documents and publications are incorporated herein by reference to the same extent as if each individual document or publication was specifically and individually incorporated herein by reference.

The foregoing description is illustrative of particular embodiments of the invention, but is not meant to be a limitation upon the practice thereof. The following claims, including all equivalents thereof, are intended to define the scope of the invention.

	Number	Date	Country
	60836103	Aug 2006	US
	60905357	Mar 2007	US

	Number	Date	Country
Parent	11835054	Aug 2007	US
Child	11926755		US

PROCESS FOR SELF-ASSEMBLY OF STRUCTURES IN A LIQUID

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