Abstract:This review deals with short peptides (up to 50 amino acids) as biomimetic active recognition elements in sensing systems. Peptide-based sensors have been developed in recent years according to different strategies. Synthetic peptides have been designed on the basis of known interactions between single or a few amino acids and targets, with attention being paid to the presence of peptide motifs known to allow intermolecular self-organization of the sensing peptides over the sensor surface. Sensitive and sophis… Show more
“…[6][7][8][9][10] Driven by a clinical need for pointof-care diagnostics, next-generation biosensors with improved sensitivity and specificity have attracted increasing attention in recent years, leading to the development of peptide-based sensing approaches. 11 Peptides derived from phage display are attractive alternatives to biosensor probes. Compared to other sensing probes (e.g., antibodies), peptides can be readily synthesized and manipulated to optimize the target specificity; thus, peptides have high affinity and specificity for target analytes, even in a complex mixture and in minute amounts.…”
Section: Introductionmentioning
confidence: 99%
“…Compared to other sensing probes (e.g., antibodies), peptides can be readily synthesized and manipulated to optimize the target specificity; thus, peptides have high affinity and specificity for target analytes, even in a complex mixture and in minute amounts. [11][12][13] More recently, biosensors based on peptides obtained through phage display have been applied for the detection of cardiac troponin I. 14 In our previous work, we showed an electrochemical biosensor using a gold electrode through a self-assembled monolayer (SAM).…”
“…[6][7][8][9][10] Driven by a clinical need for pointof-care diagnostics, next-generation biosensors with improved sensitivity and specificity have attracted increasing attention in recent years, leading to the development of peptide-based sensing approaches. 11 Peptides derived from phage display are attractive alternatives to biosensor probes. Compared to other sensing probes (e.g., antibodies), peptides can be readily synthesized and manipulated to optimize the target specificity; thus, peptides have high affinity and specificity for target analytes, even in a complex mixture and in minute amounts.…”
Section: Introductionmentioning
confidence: 99%
“…Compared to other sensing probes (e.g., antibodies), peptides can be readily synthesized and manipulated to optimize the target specificity; thus, peptides have high affinity and specificity for target analytes, even in a complex mixture and in minute amounts. [11][12][13] More recently, biosensors based on peptides obtained through phage display have been applied for the detection of cardiac troponin I. 14 In our previous work, we showed an electrochemical biosensor using a gold electrode through a self-assembled monolayer (SAM).…”
“…[2][3][4][5] Peptides binding specific targets and selected by screening of combinatorial libraries have shown great potential as antibody-mimicking affinity ligands because of their versatile chemical and physical properties in addition to well-known synthetic approaches. [6][7] In the past, our research group has developed oligopeptide sequences with binding properties towards targets as estrogens [8], mycotoxins [9,10] and recombinant proteins [11]. Their high binding capacity and selectivity were obtained through a novel evolutionary combinatorial approach, based on the selection of the best sequence extracted from a starting dipeptide library screened for the binding towards a well-defined target.…”
“…Moreover, the affinity can be further enhanced by easy modifications of the peptides. 90 Meanwhile, peptides have shown excellent intrinsic stability in harsh environments (e.g. in the presence of chemical and thermal denaturants).…”
In this review, recent advances in the development of electronic detection methodologies based on non-antibody recognition elements such as functional liposomes, aptamers and synthetic peptides are discussed.
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