Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2010-2-17
pubmed:databankReference
pubmed:abstractText
The pentameric Escherichia coli enzyme 2-hydroxypentadienoic acid hydratase assembles to form a 20-nm-diameter particle comprising 60 protein subunits, arranged with 532 symmetry when crystallised at low pH in the presence of phosphate or sulphate ions. The particles form rapidly and are stable in solution during gel filtration at low pH. They are probably formed through trimers of pentamers, which are stabilised by the interaction of two phosphate ions with residues of the N-terminal domains of subunits at the 3-fold axis. Once the particles are formed at high concentrations of phosphate (or sulphate), they remain stable in solution at 20-fold lower concentrations of the anion. Guest molecules can be trapped within the hollow protein shell during assembly. The C-termini of the subunits are freely accessible on the surface of the protein cage and thus are ideal sites for addition of affinity tags or other modifications. These particles offer a convenient model system for studying the assembly of large symmetrical structures and a novel protein nanoparticle for encapsulation and cargo delivery.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1089-8638
pubmed:author
pubmed:copyrightInfo
Copyright (c) 2009 Elsevier Ltd. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
12
pubmed:volume
396
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1379-91
pubmed:meshHeading
pubmed-meshheading:20053352-Amino Acid Sequence, pubmed-meshheading:20053352-Crystallization, pubmed-meshheading:20053352-Crystallography, X-Ray, pubmed-meshheading:20053352-DNA Primers, pubmed-meshheading:20053352-Escherichia coli, pubmed-meshheading:20053352-Escherichia coli Proteins, pubmed-meshheading:20053352-Genes, Bacterial, pubmed-meshheading:20053352-Hydro-Lyases, pubmed-meshheading:20053352-Models, Molecular, pubmed-meshheading:20053352-Molecular Sequence Data, pubmed-meshheading:20053352-Nanoparticles, pubmed-meshheading:20053352-Protein Multimerization, pubmed-meshheading:20053352-Protein Stability, pubmed-meshheading:20053352-Protein Structure, Quaternary, pubmed-meshheading:20053352-Protein Structure, Tertiary, pubmed-meshheading:20053352-Protein Subunits, pubmed-meshheading:20053352-Recombinant Proteins, pubmed-meshheading:20053352-Sequence Homology, Amino Acid
pubmed:year
2010
pubmed:articleTitle
Assembly of a 20-nm protein cage by Escherichia coli 2-hydroxypentadienoic acid hydratase.
pubmed:affiliation
Division of Medicine, UCL Medical School, Centre for Amyloidosis and Acute Phase Proteins, London NW3 2PF, UK. mark.montgomery@ucl.ac.uk
pubmed:publicationType
Journal Article