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5OB3

iSpinach aptamer

Summary for 5OB3
Entry DOI10.2210/pdb5ob3/pdb
DescriptorRNA aptamer (69-MER), 4-(3,5-difluoro-4-hydroxybenzyl)-1,2-dimethyl-1H-imidazol-5-ol, POTASSIUM ION, ... (5 entities in total)
Functional Keywordsaptamer, ispinach, dfhbi, rna
Biological sourcesynthetic construct
Total number of polymer chains1
Total formula weight22908.01
Authors
Fernandez-Millan, P.,Autour, A.,Westhof, E.,Ryckelynck, M. (deposition date: 2017-06-26, release date: 2017-10-04, Last modification date: 2024-01-17)
Primary citationFernandez-Millan, P.,Autour, A.,Ennifar, E.,Westhof, E.,Ryckelynck, M.
Crystal structure and fluorescence properties of the iSpinach aptamer in complex with DFHBI.
RNA, 23:1788-1795, 2017
Cited by
PubMed Abstract: Fluorogenic RNA aptamers are short nucleic acids able to specifically interact with small molecules and strongly enhance their fluorescence upon complex formation. Among the different systems recently introduced, Spinach, an aptamer forming a fluorescent complex with the 3,5-difluoro-4-hydroxybenzylidene imidazolinone (DFHBI), is one of the most promising. Using random mutagenesis and ultrahigh-throughput screening, we recently developed iSpinach, an improved version of the aptamer, endowed with an increased folding efficiency and thermal stability. iSpinach is a shorter version of Spinach, comprising five mutations for which the exact role has not yet been deciphered. In this work, we cocrystallized a reengineered version of iSpinach in complex with the DFHBI and solved the X-ray structure of the complex at 2 Å resolution. Only a few mutations were required to optimize iSpinach production and crystallization, underlying the good folding capacity of the molecule. The measured fluorescence half-lives in the crystal were 60% higher than in solution. Comparisons with structures previously reported for Spinach sheds some light on the possible function of the different beneficial mutations carried by iSpinach.
PubMed: 28939697
DOI: 10.1261/rna.063008.117
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.004 Å)
Structure validation

226707

數據於2024-10-30公開中

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