2015
DOI: 10.1016/j.tibtech.2015.03.012
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Non-immunoglobulin scaffolds: a focus on their targets

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Cited by 173 publications
(143 citation statements)
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“…The high-affinity binders are then selected by phage display or, recently, by ribosome display (24). Examples of such scaffold-protein affinity reagents (SPARs) (25) include DARPins (designed ankyrin repeat proteins). (26), monobodies, designed on the scaffold of human fibronectin III domain 3 (27), and also Affibody molecules (28) and anticalins (29).…”
Section: Nanobodies Versus Specific Binding Proteins Designed On Non-mentioning
confidence: 99%
“…The high-affinity binders are then selected by phage display or, recently, by ribosome display (24). Examples of such scaffold-protein affinity reagents (SPARs) (25) include DARPins (designed ankyrin repeat proteins). (26), monobodies, designed on the scaffold of human fibronectin III domain 3 (27), and also Affibody molecules (28) and anticalins (29).…”
Section: Nanobodies Versus Specific Binding Proteins Designed On Non-mentioning
confidence: 99%
“…6,7 The last years have witnessed a large number of studies attempting at developing label-free biosensors alternative to currently used platforms based on optical response. [8][9][10][11][12][13][14][15] As for IL-6, the latest reported biosensors that allow for a real-time monitoring of the cytokine levels without requiring secondary [33][34][35][36][37] .…”
Section: Introductionmentioning
confidence: 99%
“…However, artificial proteins for binding are usually smaller (i.e., <100 amino-acid residues) than antibodies. They have high stability with deficiency of disulfide bonds in contrast to antibodies [16,17]. Artificial proteins are thus a promising candidate to create biosensors [18,19].…”
Section: Antibody/antigen Interactionsmentioning
confidence: 99%