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Biochem Biophys Res Commun ; 517(1): 146-154, 2019 09 10.
Article in English | MEDLINE | ID: mdl-31351587

ABSTRACT

The phosphinositide PtdIns(3)P plays an important role in autophagy; however, the detailed mechanism of its activity remains unclear. Here, we used a Systematic Evolution of Ligands by EXponential enrichment (SELEX) screening approach to identify an RNA aptamer of 40 nucleotides that specifically recognizes and binds to intracellular lysosomal PtdIns(3)P. Binding occurs in a magnesium concentration- and pH-dependent manner, and consequently inhibits autophagy as determined by LC3II/I conversion, p62 degradation, formation of LC3 puncta, and lysosomal accumulation of Phafin2. These effects in turn inhibited lysosomal acidification, and the subsequent hydrolytic activity of cathepsin D following induction of autophagy. Given the essential role of PtdIns(3)P as a key targeting molecule for autophagy induction, identification of this novel PtdIns(3)P RNA aptamer provides new opportunities for investigating the biological functions and mechanisms of phosphoinositides.


Subject(s)
Aptamers, Nucleotide/metabolism , Phosphatidylinositol Phosphates/metabolism , Aptamers, Nucleotide/chemistry , Aptamers, Nucleotide/pharmacology , Autophagy/drug effects , Base Sequence , Cell Line , Humans , Lysosomes/drug effects , Lysosomes/metabolism , SELEX Aptamer Technique , Vesicular Transport Proteins/metabolism
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