Quantitative in vivo solubility and reconstitution of truncated circular permutants of green fluorescent protein
β Scribed by Yao-Ming Huang; Sasmita Nayak; Christopher Bystroff
- Book ID
- 105356739
- Publisher
- Cold Spring Harbor Laboratory Press
- Year
- 2011
- Tongue
- English
- Weight
- 474 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0961-8368
- DOI
- 10.1002/pro.735
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β¦ Synopsis
Abstract
Several versions of split green fluorescent protein (GFP) fold and reconstitute fluorescence, as do many circular permutants, but little is known about the dependence of reconstitution on circular permutation. Explored here is the capacity of GFP to fold and reconstitute fluorescence from various truncated circular permutants, herein called βleaveβoneβoutsβ using a quantitative in vivo solubility assay and in vivo reconstitution of fluorescence. Twelve leaveβoneβout permutants are discussed, one for each of the 12 secondary structure elements. The results expand the outlook for the use of permuted split GFPs as specific and selfβreporting gene encoded affinity reagents.
π SIMILAR VOLUMES
We have constructed three plasmid vectors for the expression of green fluorescent protein (GFP) fusion proteins using the following motif: (His) 6 -GFP-EK-X, where X represents chloramphenicol acetyl-transferase (CAT), human interleukin-2 (hIL-2), and organophosphorous hydrolase (OPH), respectively,