Miniproteins as phage display-scaffolds for clinical applications

Miniproteins are currently developed as alternative, non-immunoglobin proteins for the generation of novel binding motifs. Miniproteins are rigid scaffolds that are stabilised by alpha-helices, beta-sheets and disulfide-constrained secondary structural elements. They are tolerant to multiple amino a...

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Bibliographic Details
Main Authors: Zoller, Frederic (Author) , Haberkorn, Uwe (Author) , Mier, Walter (Author)
Format: Article (Journal)
Language:English
Published: 14 March 2011
In: Molecules
Year: 2011, Volume: 16, Issue: 3, Pages: 2467-2485
ISSN:1420-3049
DOI:10.3390/molecules16032467
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/molecules16032467
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/1420-3049/16/3/2467
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Author Notes:Frederic Zoller, Uwe Haberkorn and Walter Mier
Description
Summary:Miniproteins are currently developed as alternative, non-immunoglobin proteins for the generation of novel binding motifs. Miniproteins are rigid scaffolds that are stabilised by alpha-helices, beta-sheets and disulfide-constrained secondary structural elements. They are tolerant to multiple amino acid substitutions, which allow for the integration of a randomised affinity function into the stably folded framework. These properties classify miniprotein scaffolds as promising tools for lead structure generation using phage display technologies. Owing to their high enzymatic resistance and structural stability, miniproteins are ideal templates to display binding epitopes for medical applications in vivo. This review summarises the characteristics and the engineering of miniproteins as a novel class of scaffolds to generate of alternative binding agents using phage display screening. Moreover, recent developments for therapeutic and especially diagnostic applications of miniproteins are reviewed.
Item Description:Gesehen am 23.01.2023
Physical Description:Online Resource
ISSN:1420-3049
DOI:10.3390/molecules16032467