Figure 1 Template-map sets used to generate a set of 108 8mers that contain 50% G/C content and are 4bm complements and reversals. 8mers are generated.

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Presentation transcript:

Figure 1 Template-map sets used to generate a set of 108 8mers that contain 50% G/C content and are 4bm complements and reversals. 8mers are generated by crossing each template with each map using the following rule: for each position in a map with a 1, the corresponding position in the template is changed to the complementary base, while for each position in a map with a 0, the corresponding position in the template is unchanged. From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

1 From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Figure 2 Reaction scheme showing the surface attachment chemistry of HS-DNA onto chemically modified gold films. The gold surface is modified with a monolayer of 11-mercaptoundecanoic acid (MUA) followed by the electrostatic adsorption of a poly-l-lysine monolayer (PL). This amine-terminated surface is then reacted with the bifunctional linker SSMCC, creating a thiol-reactive maleimide surface which is subsequently reacted with single-stranded 5′-thiol modified DNA. From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

5 From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

2 From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

3 From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

4 From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Table 1 Inherent and slide matches for the 108 set with the word label GCTT........TTCG From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Table 2 Oligonucleotides used in the four spot fluorescence experiments From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Figure 3 Arrangement of 4 DNA words attached to a chemically modified gold surface used in the four spot fluorescence experiments. The sequences of the words are listed in Table 2 From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Table 3 Experimental and predicted T<sub>m</sub><sup>a</sup> for various duplexes From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Figure 4 Four spot fluorescence imaging measurements on a representative set of 4 DNA words. Hybridization adsorption to the four word set was studied by the sequential exposure of the surface to each of the fluorescent complements. Between each exposure step, the surface was regenerated by exposure to urea. The far right column shows the internal bits of the surface bound words (top sequence) and the fluorescein-labeled complements (bottom sequence) in each hybridization step; perfect match duplexes are shown in blue, and mismatched bases are shown as red, underlined letters. Note that for each hybridization step, only the perfect match was observed after washing the surface in buffer at 37°C for 5 min. From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Table 4 Classification and predicted thermodynamics of 4 base mismatches (4bm) using Method 1 From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Figure 5 Word label discrimination experiment Figure 5 Word label discrimination experiment. Two 16mer words with the same internal 8mer sequence were immobilized onto a chemically modified gold surface and then sequentially exposed to the fluorescein-labeled complement of each word. Mismatched base pairs are shown as red, underlined letters. Discrimination was achieved by rinsing the surface in buffer solution for 5 min at 37°C. From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press

Figure 6 Selective enzymatic destruction experiment Figure 6 Selective enzymatic destruction experiment. A surface with the 4 DNA words W1-W4 arranged as depicted in Figure 3 was prepared and then exposed to a solution containing the set of fluorescein-labeled complements C1-C4 (i.e. the operation ‘Mark All’) giving the image shown in ( A ). The surface then underwent the following series of operations to give the image shown in ( B ): 1. Unmark: the removal of all hybridized complements; 2. Mark {W2, W3, W4}: exposure to a solution containing the complements to W2, W3, W4; 3. Destroy: exposure to a solution of the single-strand-specific enzyme Exonuclease I; 4. Unmark; 5. Mark All. This series of operations was repeated two more times to remove W2 and W4 as shown in ( C ) and ( D ) respectively. Exonuclease digestion removed >94% of W1, W2 and W4. From: Demonstration of a word design strategy for DNA computing on surfaces Nucleic Acids Res. 1997;25(23):4748-4757. doi:10.1093/nar/25.23.4748 Nucleic Acids Res | © 1997 Oxford University Press