LCP-Tm: An assay to measure and understand stability of membrane proteins in a membrane environment

Wei Liu, Michael A. Hanson, Raymond C. Stevens, Vadlm Cherezov

Research output: Contribution to journalArticlepeer-review

52 Scopus citations


Structural and functional studies of membrane proteins are limited by their poor stability outside the native membrane environment. The development of novel methods to efficiently stabilize membrane proteins immediately after purification is important for biophysical studies, and is likely to be critical for studying the more challenging human targets. Lipidic cubic phase (LCP) provides a suitable stabilizing matrix for studying membrane proteins by spectroscopic and other biophysical techniques, including obtaining highly ordered membrane protein crystals for structural studies. We have developed a robust and accurate assay, LCP-Tm, for measuring the thermal stability of membrane proteins embedded in an LCP matrix. In its two implementations, protein denaturation is followed either by a change in the intrinsic protein fluorescence on ligand release, or by an increase in the fluorescence of a thiol-binding reporter dye that measures exposure of cysteines buried in the native structure. Application of the LCP-Tm assay to an engineered human β2-adrenergic receptor and bacteriorhodopsin revealed a number of factors that increased protein stability in LCP. This assay has the potential to guide protein engineering efforts and identify stabilizing conditions that may improve the chances of obtaining high-resolution structures of intrinsically unstable membrane proteins.

Original languageEnglish (US)
Pages (from-to)1539-1548
Number of pages10
JournalBiophysical journal
Issue number8
StatePublished - Apr 21 2010
Externally publishedYes

ASJC Scopus subject areas

  • Biophysics


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