2016
DOI: 10.1016/j.msec.2016.06.060
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Self-assembling peptide hydrogels immobilized on silicon surfaces

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Cited by 4 publications
(4 citation statements)
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“…1e. The position of the single component at the binding energy of 400.3 eV corresponded to expected value for peptidic nitrogen atoms [23,24]. Both the C 1s and N 1s spectra confirm the binding of HELP coating on both borosilicate and Fig.…”
Section: Helps Primary Structures and Coatingssupporting
confidence: 63%
“…1e. The position of the single component at the binding energy of 400.3 eV corresponded to expected value for peptidic nitrogen atoms [23,24]. Both the C 1s and N 1s spectra confirm the binding of HELP coating on both borosilicate and Fig.…”
Section: Helps Primary Structures and Coatingssupporting
confidence: 63%
“…Here, we used the N K-edge of EP1-EP5 samples deposited on CVD graphene to probe the amide π orbital functionality along the peptide backbone, aiming to obtain an overall molecular orientation on the surface. [50][51][52] It is worth mentioning that the amino acid residues from peptides interact non-covalently with CNT and graphene in the same qualitative way, mainly through π-π stacking interactions. [53] The difference emerges in this interaction's magnitude, reportedly weaker for CNT than graphene.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, our carbon K-edge spectra were further calibrated using the resonance at 285.50 eV assigned to the C1s π* ring transition. The spectra were then normalized subtracting a straight line that fits the part of the spectrum below the edge and assessing to 1 the value at 320.00 eV and 425.00 eV for carbon and nitrogen, respectively [ 48 ].…”
Section: Methodsmentioning
confidence: 99%
“…Furthermore a possible strategy to promote osseo-integration and enhance the biological acceptance of the implants is the biofunctionalization of the Ti25Nb10Zr surface with bioactive molecules that can be grafted on the surface in order to establish a molecular dialogue with host cells [ 47 ]. Among other bioactive molecules, self-assembling peptides (SAPs) are extremely promising candidates, since thanks to their on-purpose designed sequence they are able to self-assemble in a beta-sheet secondary structure [ 48 , 49 ]. They can then aggregate in the presence of saline creating hydrogels that can be used either as drug delivery vehicles, in the case of factors to release with a precise kinetic, or can be decorated with adhesive sequences or proteins, appropriately conjugated with a self-assembling sequence, allowing the functionalization of the scaffold with adhesive signals in a 3D structure by simple co-aggregation.…”
Section: Introductionmentioning
confidence: 99%