<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bin Mohamed Suffian IF</submitter><funding>Biotechnology and Biological Sciences Research Council</funding><pagination>43160</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5335696</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>An E. coli expression system offers a mean for rapid, high yield and economical production of Hepatitis B Virus core (HBc) particles. However, high-level production of HBc particles in bacteria is demanding and optimisation of HBc particle yield from E. coli is required to improve laboratory-scale productivity for further drug delivery applications. Production steps involve bacterial culture, protein isolation, denaturation, purification and finally protein assembly. In this study, we describe a modified E. coli based method for purifying HBc particles and compare the results with those obtained using a conventional purification method. HBc particle morphology was confirmed by Atomic Force Microscopy (AFM). Protein specificity and secondary structure were confirmed by Western Blot and Circ</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Yield Optimisation of Hepatitis B Virus Core Particles in E. coli Expression System for Drug Delivery Applications.</pubmed_title><pmcid>PMC5335696</pmcid><funding_grant_id>BB/J008656/1</funding_grant_id><pubmed_authors>Brown P</pubmed_authors><pubmed_authors>Bui T</pubmed_authors><pubmed_authors>Nishimura Y</pubmed_authors><pubmed_authors>Garcia-Maya M</pubmed_authors><pubmed_authors>Palermo AR</pubmed_authors><pubmed_authors>Bin Mohamed Suffian IF</pubmed_authors><pubmed_authors>Al-Jamal KT</pubmed_authors><pubmed_authors>Kondo A</pubmed_authors><pubmed_authors>Ogino C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Yield Optimisation of Hepatitis B Virus Core Particles in E. coli Expression System for Drug Delivery Applications.</name><description>An E. coli expression system offers a mean for rapid, high yield and economical production of Hepatitis B Virus core (HBc) particles. However, high-level production of HBc particles in bacteria is demanding and optimisation of HBc particle yield from E. coli is required to improve laboratory-scale productivity for further drug delivery applications. Production steps involve bacterial culture, protein isolation, denaturation, purification and finally protein assembly. In this study, we describe a modified E. coli based method for purifying HBc particles and compare the results with those obtained using a conventional purification method. HBc particle morphology was confirmed by Atomic Force Microscopy (AFM). Protein specificity and secondary structure were confirmed by Western Blot and Circ</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2026-05-30T04:21:34.351Z</modification><creation>2019-03-27T02:37:46Z</creation></dates><accession>S-EPMC5335696</accession><cross_references><pubmed>28256592</pubmed><doi>10.1038/srep43160</doi></cross_references></HashMap>