General qPCR and plate reader methods for rapid optimization of membrane protein purification and crystallization using thermostability assays

Thomas M. Tomasiak, Bjørn P. Pedersen, Sarika Chaudhary, Andrew Rodriguez, Yaneth Robles Colmanares, Zygy Roe-Zurz, Sobha Thamminana, Meseret Tessema, Robert M. Stroud

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

This unit describes rapid and generally applicable methods to identify conditions that stabilize membrane proteins using temperature-based denaturation measurements as a proxy for target time-dependent stability. Recent developments with thiol-reactive dyes sensitive to the unmasking of cysteine residues upon protein unfolding have allowed for routine application of thermostability assays to systematically evaluate the stability of membrane protein preparations after various purification procedures. Test conditions can include different lipid cocktails, lipid-detergent micelles, pH, salts, osmolytes, and potential active-site ligands. Identification and use of conditions that stabilize the structure have proven successful in enabling the structure determination of numerous families of membrane proteins that otherwise were intractable.

Original languageEnglish (US)
Pages (from-to)29.11.1-29.11.14
JournalCurrent Protocols in Protein Science
Volume2014
DOIs
StatePublished - 2014
Externally publishedYes

Keywords

  • Dye-based assay
  • Membrane proteins
  • Thermostability

ASJC Scopus subject areas

  • Structural Biology
  • Biochemistry

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