Dufva et al introduced standard protocol for grafting agarose layer on to unmodified glass microscope slides. AFM characterization of grafted agarose film demonstrated a significant increase in surface roughness. SEM analysis showed the porous structure of agarose. Amino-modified 21 and 25 bp long capture probes were immobilized on activated agarose surface. Agarose-coated slides had the highest signal-to-noise ratio in hybridization. In addition, UV immobilization of DNA probes on to agarose surface on glass slides further increased the signal-to-noise ratio ⁽¹⁹⁾.

In the research of Wei et al a thin film of oxidized agarose was prepared on the surface of ordinary glass slides as antibody/antigen microarray substrate. The aldehyde groups derived from the agarose film were covalently linked with amino groups of antigens. AFM characterization and assay results demonstrated that gel assembly film was a surface of three-dimensional structure. The enzyme immunoassay system on the substrates was successfully developed. These microchips could provide simultaneous analysis for multi-auto-antibodies ⁽²¹⁾.

Koch and his co-workers spotted amine-modified oligonucleotides on the surface of activated agarose-coated slides using a manual eight-pin arraying device. The probes easily distinguished different plant pathogens from each other without cross section. Spotted probes on agarose differentiated samples as readily as probes on nylon but with potentially higher spot density and gave much higher signal than probes on silanated slides ⁽²²⁾.

In another study, Dufva et al ascertained that 13- to 17- base oligonucleotide tagged with a poly(T) 10-poly(C) 10 tail, but otherwise unmodified, could be crosslinked by UV irradiation to an agarose film grafted on to unmodified glass. These microarrays were used to diagnose mutations in the human β-globin gene. Sufficiently high discrimination signals were obtained between perfect match and mismatch probes in hybridization.

Xu et al developed a new kind of sensitive substrates by coating agarose on silica opal film fabricated on glass substrate. These substrates provided stronger fluorescence signals compared with agarose on unmodified glass and thus improved detection sensitivity ⁽²³⁾.

Microscope glass slides (25.4 mm×76.2 mm×1 mm) and glass cover slips were purchased from Sigma-Aldrich. PLL was purchased from Sigma and Agarose was provided by Roche. Betaine, Sodium Diodecyl Sulfate (SDS), Succinic Anhydride (SA), N-Methyl 2-Pyrrolidone (NMP), Boric acid, Sodium hydroxide (NaOH), Ethanol, Bovine Serum Albumin (BSA), Formamide and Salmon sperm DNA were purchased from Sigma. Saline sodium citrate was provided by Ambion. Sodium periodate was purchased from Fluka. DNA extraction kits were purchased from Tadbir Fan Azma Co. Cy5mono-reactive dye was purchased from GE-Healthcare. Finally, DNA labeling kits were provided by Agilent Technologies Co.

Three different polymeric layers were coated on the standard glass slides: (i) PLL, (ii) Agarose, and (iii) Agarose layer on the PLL coating.

After cleaning of microscope slides by a mixed solution of NaOH and ethanol, the slides were rinsed in dH₂O. For coating of PLL polymer on cleaned slides, PLL fresh coating solution was prepared by mixing 1:9 ratio of PLL and dH₂O, respectively. The slides were covered with the solution for 1 hr on an orbital shaker (50 rpm, Cole Parmer Economic orbital shaker). The slides were transferred in to slide centrifuge (Arrat It^® microarray high speed centrifuge) for liquid collection. Then, slides were placed in vaccum oven (43°C, Memmert) for complete drying. Agarose layer was also coated on unmodified glass slides and PLL-coated glass slides according to method described by Dufva et al ⁽¹⁹⁾.

DNA probes, which have 35-40 bp long (Table 1) were spotted on the fabricated substrates using Q-array mini system (Genetix, Germany). Printing solution, containing 150 mM of phosphate buffer, pH = 8.5 and 3X SSC with 1.5 M Betaine wasprepared. Dried probes were suspended in the mixture of equal volume of printing buffer and dH₂O to obtain final concentration of ∼ 200 ng/µl.

Substrates were printed at 40-50% relative humidity, and then dried in the air for 10 min. The probes were spotted in quadruplicate on the substrates. The DNA probes were immobilized on the slides by UV radiation at 254 nm using a CL-1000 UV crosslinker (UVP Inc.) for 3 min. Then, arrays were immersed in 1% Sodium Diodecylsulphate (SDS) for 30 s. Finally, the slides were dried using compressed nitrogen gas.

The micro-scale micrographs of the spotted and unspotted glass slides were obtained using AIS2100 Scanning Electron Microscopy (Seron Technology Inc., Korea). A Hysitron Inc. (USA) Triboscope^® Nanomechanical test instrument with 2D transducer, complete soft-ware and Berkovich diamond indenter were used to measure reduced elastic modulus (E_r) and hardness (H) of the coated and uncoated glass slides. Five measurements were performed in the peripheral and central parts of the slides. The AFM (Atomic Force Microscope) part and a Nanoscope E (Digital Instruments, USA) were used to obtain images of the surface. The AFM images were analyzed using Nanoscope^® software version III 5.12r2. Mean roughness (R_a), root-mean square roughness (R_ms), maximum height (R_max) and 3D surface area (R_area) were calculated using this software.

Genomic DNA was extracted from peripheral blood using TadbirFan Azma DNA extraction kit (Iran). For labeling genomic DNA, 2 µg of DNA was added to dH₂O to bring total volume to 21 µl. Then, 20 µl of 2.5X random primer/reaction buffer was added. The mixture was boiled for 5 min, and then placed on ice. 5 µl of 10X dNTP was added on ice. Then, 3 µl of cy5-dCTP dye and 1 µl of Klenow fragment were added. The mixture was incubated at 37 °C for 2 hr. The reaction was stopped by adding 5 µl of 0.5 M EDTA at pH = 8.0.

Hybridization solution was prepared according to Table 2. Pre-hybridization of the slides was done to eliminate non-specific binding of target to the slides. The slides were immersed in hybridization solution and incubated at 42°C for 1 hr in a water bath. Then, the pre-hybridized slides were washed in dH₂O and dried using compressed nitrogen gas.

Labeled DNA target was diluted in hybridization solution to 10 nM final concentration. The microarrays were hybridized with appropriate amount of target under cover slips in incubator at 42°C 5 hr until spots saturated. Then, the slides were immersed in the solution 2X SSC and 0.1% SDS and washed in 1X SSC for 1 min, in 0.2X SSC for 1 min and 0.05X SSC for 1-2 s and finally rinsed in dH₂O and dried using compressed nitrogen gas.

The hybridized microarrays were scanned using Scan Array GX Microarray Scanner (Perkin Elmer). Spots were quantified from the images generated from Scan Array GX Microarray software (Perkin Elmer) using Scan Analyze software version 2.5. For calculating signal-to-noise ratio (SNR) of spots, the following formula was employed: SNR = SM - BM Standard deviation of background

where SM was mean signal of four spots which replicated each probe when hybridized to cy5 labeled target and BM was mean background signal.

PLL used to coat glass slides for preparing microarrays can attach to glass slides more strongly than agarose layer. But PLL-coated surfaces have low binding capacity for biomolecules. Activated agarose provided a thin layer on the glass with active aldehyde groups which can bind to amino groups on various biomolecules, such as DNA, proteins, peptides and phospholipids. In addition to providing active groups on the surface, agarose could perform a physical function; it provided a uniform three-dimensional solid support for dynamic attaching of biomolecules. Activated agarose thin film on the PLL-coated glass slides resulted in chemical binding between two polymer layers; therefore, agarose could attach to PLL-coated slides more strongly than unmodified slides. Therefore, higher stability in hybridization reactions and higher signal-to-noise ratio were provided.

The surface profiles of the coated and uncoated glasses characterized by AFM showed that agarose provided three-dimensional thin film on the unmodified and PLL-coated glass slides (Figures 1A and 2A). The mean roughness (R_a), root-mean square roughness (R_ms), maximum height (R_max) and 3D surface area (R_area) for agarose-PLL coated, agarose coated and PLL-coated glass were reported in Table 3. The section analysis of agarose-PLL coated, agarose coated and PLL-coated slides revealed that their vertical distance were 35.520 and 33.504 nm, respectively (Figures 1C, 2C and 3C), while vertical distance of PLL-coated surface was 0.817 nm. The distance demonstrated the thickness of thin polymeric films on glass surface.

The mean reduced elastic modulus (E_r) and mean hardness (H) were calculated from five indentations performed in peripheral and central parts of surface and were reported in Table 4 for agarose on PLL-coated slides, agarose on unmodified glass and unmodified glass. The nano-indentation measurements on the surfaces ascertained the impressibility and softness of prepared substrate surface which was essential for spotter pins’ safety. Although, agarose coatings were applied manually to the surface, five different measurements showed that agarose layers were relatively uniform. The difference between mechanical properties of agarose-PLL in comparison with PLL two-dimensional layers was related to three-dimensional agarose structure on the surface. PLL is a polymer which can reduce hardness of the coated surface; therefore, the difference between the mechanical properties of agarose-PLL and agarose coatings and also the difference between PLL-coated and unmodified glass surfaces were related to coating by PLL polymeric layer.

SEM analysis of the agarose on the glass slides showed a porous film (Figure 4). In addition, this micrograph demonstrated that the orientation of agarose film was parallel to glass surface.

The SEM micrograph of the prepared microarrays on three different coated substrates showed spots written on the agarose layers were more regular than spots on the PLL-coated slides in shape and size (Figures 5A, B and C). Some spots on the PLL-coated substrate had an inappropriate quality and were ununiformed in diameter. It is worth mentioning that spots on the agarose had better quality (Figures 6A, B and C). The spot diameter was between 200-250 µm.

The activated agarose layer grafted to PLL-coated on the glass surface could sustain incubation at 37°C for 6.5 hr and at 50°C for 5 hr. Also, we examined the stability of aga-rose layer on the unmodified glass slides; it could sustain incubation at 37°C for 3 hr and at 50°C for 1 hr without rehydration and detaching from the slides. These slides can be stable in hybridization of biomolecules, such as proteins, peptides and oligonucleotides to microarrays.

The slides coated using activated agarose and agarose-PLL film showed significant increase in signal and signal-to-noise ratio in comparison with slides coated using PLL alone (Figures 7A and C). Also, background signal from substrate was higher in PLL-coated slides than two slides coated using agarose. The agarose layer on PLL-coated substrate showed the best hybridization signal (Figure 7B). The agarose-PLL coated substrates had a 4-fold and 2-fold increase in SNR compared with PLL-coated slides and agarose-coated slides, respectively. These results demonstrated that agarose-PLL coated slides are suitable for analyzing wide concentration range analytes.