Circular proteins - no end in sight


Autoria(s): Trabi, Manuela; Craik, David J.
Data(s)

01/03/2002

Resumo

Circular proteins are a recently discovered phenomenon. They presumably evolved to confer advantages over ancestral linear proteins while maintaining the intrinsic biological functions of those proteins. In general, these advantages include a reduced sensitivity to proteolytic cleavage and enhanced stability. In one remarkable family of circular proteins, the cyclotides, the cyclic backbone is additionally braced by a knotted arrangement of disulfide bonds that confers additional stability and topological complexity upon the family. This article describes the discovery, structure, function and biosynthesis of the currently known circular proteins. The discovery of naturally occurring circular proteins in the past few years has been complemented by new chemical and biochemical methods to make synthetic circular proteins; these are also briefly described.

Identificador

http://espace.library.uq.edu.au/view/UQ:64164

Idioma(s)

eng

Publicador

Elsevier Science

Palavras-Chave #Biochemistry & Molecular Biology #Polypeptide Kalata B1 #Peptide Antibiotic As-48 #Cystine-knot #Structural Motif #Membranolytic Selectivity #Macrocyclic Polypeptides #Chassalia-parvifolia #Cyclic Polypeptide #Chemical Synthesis #Escherichia-coli #C1 #250302 Biological and Medical Chemistry #670403 Treatments (e.g. chemicals, antibiotics)
Tipo

Journal Article