Time-course and degradation rate of membrane scaffold protein (MSP1D1) during recombinant production

Ramona Faas, Dirk Kiefer, Laura Job, Annelie Pohle, Karin Moß, Marius Henkel, Rudolf Hausmann

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Membrane scaffold proteins (MSPs) are synthetic derivatives of apolipoprotein A-I, a major protein component of human high-density lipoprotein complexes. The most common among these is the variant MSP1D1, which has been in the focus of research on membrane mimetics in the past. As such, the amphipathic MSP1D1 has the ability to self-assemble in the presence of synthetic phospholipids into discoidal nanoparticles, so called nanodiscs. The recombinant production of MSP is exclusively reported using a standard laboratory expression system of the pET family. However, strong variations in both yield and achieved concentration as well as complications related to unspecific degradation are commonly reported. In addition, the time-course of recombinant protein as well as specific protein yields have not yet been quantified conclusively. In this study, the time-course of MSP1D1 concentration was investigated in a standard pET expression system in terms of quantification of production and degradation rates in comparison to a reference protein (eGFP).

Original languageEnglish
Pages (from-to)45-48
Number of pages4
JournalBiotechnology Reports
Volume17
DOIs
StatePublished - Mar 2018
Externally publishedYes

Keywords

  • Apolipoprotein A-I
  • Membrane scaffold protein
  • Nanodisc
  • Recombinant protein
  • pET expression system

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