Open AccessA Journey from the Pool of Chiral Synthetic Building Blocks to Cell-Penetrating Peptides, to a Novel Type of Enzyme – and back
Author(s) -
Dieter Seebàch
Publication year - 2013
Publication title -
chimia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.387
H-Index - 55
eISSN - 2673-2424
pISSN - 0009-4293
DOI - 10.2533/chimia.2013.844
Subject(s) - enantiopure drug , enzyme , peptide , amino acid , biochemistry , chemistry , internalization , peptide sequence , cell , combinatorial chemistry , enantioselective synthesis , gene , catalysis
The roles of polyhydroxy-butyrates/alkanoates (PHB/PHA) in biology, for the preparation of chiral building blocks, and as a source of inspiration for the discovery of ?- and ?-peptides are discussed. The syntheses and structures of ?-peptides are outlined. The prerequisites for mimicking peptide/protein interactions with ?-peptides and two examples are presented. Single terminal ?-amino-acid residues can lead to stabilization of peptides (cf. NTS(8-13)) in plasma. Cell-penetrating ?-L-, ?-D-, mixed ?-L/D- and ?-oligoarginines (OAs) and -oligoprolines, as well as the mechanism(s) of internalization are compared. Recent studies show that infected erythrocytes, parasitic organisms and mycobacteria are entered by OA-derivatives, which have been employed as transporters of the antibiotic fosmidomycin. While ?-peptides are generally enzymatically stable (for days in mammals), a microorganism (S. xenopeptidilytica) with an Ntn enzyme (3-2W4 BapA) was discovered that cleaves only ?-peptides, and that was applied in preparations of (enantiopure) ?-amino acids and ?-peptides.