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1.
Drug Discov Today Technol ; 26: 33-42, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29249241

ABSTRACT

In this review we provide an overview of recent developments in the field of cell penetrating peptides (CPPs) on research that aims to achieve better control over their transduction properties - one of the big challenges - by means of restraining them. Three different constraining strategies are presented: triggerable activation, backbone rigidification and macrocyclization. Each of these methods have their opportunities in gaining control over CPP activity and selectivity.


Subject(s)
Cell-Penetrating Peptides/chemistry , Peptides, Cyclic/chemistry , Animals , Cell-Penetrating Peptides/metabolism , Humans , Peptides, Cyclic/metabolism
2.
J Mater Chem B ; 3(15): 2954-2961, 2015 Apr 21.
Article in English | MEDLINE | ID: mdl-32262495

ABSTRACT

Sensing cell adhesion by means of a colourimetric response provides an intuitive measure of cell binding. In this study polydiacetylene-containing peptide amphiphiles fibres were designed to sense cell adhesion by means of a colour change. The diacetylene-containing peptide amphiphiles were functionalised with the cell-binding motif RGDS, and subsequently mixed with non-functionalised diacetylene-containing spacer amphiphiles. The diacetylenes in the backbone of these fibres were polymerised using UV-light to give dark blue fibre solutions. Subsequent cell adhesion induced a colour change from blue to pink. The propensity of the RGDS fibres to change colour upon cell adhesion could be tuned by varying the C-terminal amino acid of the spacer amphiphile. In addition to this, by varying the RGDS density we found that the optimum colourimetric response was obtained for fibres with a 6 : 1 ratio of non-RGDS to RGDS amphiphiles.

3.
Chem Soc Rev ; 43(8): 2743-56, 2014 Apr 21.
Article in English | MEDLINE | ID: mdl-24448606

ABSTRACT

Proteins and peptides are fundamental components of living systems where they play crucial roles at both functional and structural level. The versatile biological properties of these molecules make them interesting building blocks for the construction of bio-active and biocompatible materials. A variety of molecular tools can be used to fashion the peptides necessary for the assembly of these materials. In this tutorial review we shall describe five of the main techniques, namely solid phase peptide synthesis, native chemical ligation, Staudinger ligation, NCA polymerisation, and genetic engineering, that have been used to great effect for the construction of a host of peptide-based materials.


Subject(s)
Biocompatible Materials/chemistry , Peptides/chemistry , Drug Carriers/chemistry , Genetic Engineering , Humans , Hydrogel, Polyethylene Glycol Dimethacrylate/chemistry , Microscopy, Electron, Transmission , Nanocapsules/chemistry , Peptides/chemical synthesis
4.
Faraday Discuss ; 166: 360-79, 2013.
Article in English | MEDLINE | ID: mdl-24611288

ABSTRACT

Peptide amphiphiles consisting of a hydrophobic alkyl tail coupled to the eight-amino acid GANPNAAG have been studied extensively for their fibre forming properties. However, detailed characteristics of the fibre structure, such as peptide conformation and molecular organisation, are unknown to date. In this report a range of characterization techniques is described that have been employed to elucidate the internal structure of these fibres. Based on the results obtained by circular dichroism spectroscopy, X-ray diffraction and solid state NMR spectroscopy it was concluded that in a self-assembled state the peptide is in a stretched beta-sheet conformation, with the alkyl tails interdigitated and hydrogen-bonded along the axis of the fibre.


Subject(s)
Palmitic Acid/chemistry , Peptides/chemistry , Circular Dichroism , Microscopy, Electron, Transmission , Protein Conformation , X-Ray Diffraction
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