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A green fluorescent protein screen for identification of well‐expressed membrane proteins from a cohort of extremophilic organisms
Author(s) -
Hammon Justus,
Palanivelu Dinesh V.,
Chen Joy,
Patel Chintan,
Minor Daniel L.
Publication year - 2009
Publication title -
protein science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.353
H-Index - 175
eISSN - 1469-896X
pISSN - 0961-8368
DOI - 10.1002/pro.18
Subject(s) - green fluorescent protein , membrane protein , fusion protein , biology , protein expression , fluorescence , membrane , microbiology and biotechnology , biochemistry , computational biology , gene , recombinant dna , physics , quantum mechanics
Green fluorescent protein (GFP) fusion proteins provide a potentially facile tool for identification of well expressed, properly behaved membrane proteins for biochemical and structural study. Here, we present a GFP‐expression survey of >300 membrane proteins from 18 bacterial and archaeal extremophiles, organisms expected to be rich sources of membrane proteins having robust biophysical properties. We find that GFP‐fusion fluorescence intensity is an excellent indicator of over‐expression potential. By employing a follow‐up optimization protocol using a suite of non‐GFP constructs and different expression temperatures, we obtain 0.5–15 mg L −1 expression levels for 90% of the tested candidate proteins that pass the GFP screen. Evaluation of the results suggests that certain organisms may serve as better sources of well‐expressed membrane proteins than others, that the degree to which codon usage matches the expression host is uncorrelated with success rate, and that the combination of GFP screening and expression optimization is essential for producing biochemically tractable quantities of material.