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The peak corresponding to the stretch of the carboxylate moiety present in PM-IRRAS spectra collected after RGESP conjugation is due to the carboxylate group on the side chain of glutamic acid introduced on the surface as a result of peptide conjugation
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The peak corresponding to the stretch of the carboxylate moiety present in PM-IRRAS spectra collected after RGESP conjugation is due to the carboxylate group on the side chain of glutamic acid introduced on the surface as a result of peptide conjugation.
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An additional notable observation is that the amide I peak area after CuAAC was greater than the amide I peak area after carbodiimide condensation at each alkanethiolate mole fraction characterized. This observation suggests that the molar ratio of azide to carboxylate groups in the resulting SAM is greater than the molar ratio of azide to carboxylate groups in ethanol during SAM formation for all conditions studied. This observation is consistent with previous results that demonstrated that the rate of adsorption of HS-EG6-N3 (kN3) onto gold is significantly faster than the rate of adsorption of HS-EG6-EG3 (kEG3) onto gold (ref 7), and suggests that preferential HS-EG6-N3 adsorption onto gold may also occur in the presence of HS-EG6-COOH
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An additional notable observation is that the amide I peak area after CuAAC was greater than the amide I peak area after carbodiimide condensation at each alkanethiolate mole fraction characterized. This observation suggests that the molar ratio of azide to carboxylate groups in the resulting SAM is greater than the molar ratio of azide to carboxylate groups in ethanol during SAM formation for all conditions studied. This observation is consistent with previous results that demonstrated that the rate of adsorption of HS-EG6-N3 (kN3) onto gold is significantly faster than the rate of adsorption of HS-EG6-EG3 (kEG3) onto gold (ref 7), and suggests that preferential HS-EG6-N3 adsorption onto gold may also occur in the presence of HS-EG6-COOH.
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3. Based on the Stokes radius calculated from the estimated peptide volume, and assuming homogeneous alkanethiolate packing, the maximal packing of the peptide should be observed at ∼11.4% COOH. In contrast, our experiments indicate a maximum packing density between 5% and 7.5% COOH. The discrepancy could be explained by variation from theoretical calculations in the peptide Stokes radius or heterogeneous SAM packing
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3. Based on the Stokes radius calculated from the estimated peptide volume, and assuming homogeneous alkanethiolate packing, the maximal packing of the peptide should be observed at ∼11.4% COOH. In contrast, our experiments indicate a maximum packing density between 5% and 7.5% COOH. The discrepancy could be explained by variation from theoretical calculations in the peptide Stokes radius or heterogeneous SAM packing.
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