Your browser doesn't support javascript.
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
1.
Biosci Biotechnol Biochem ; 85(5): 1170-1174, 2021 Apr 24.
Article in English | MEDLINE | ID: covidwho-1010330

ABSTRACT

Interleukin-6 (IL-6) binds to the IL-6 receptor (IL-6R) subunit, related to autoimmune diseases and cytokine storm in COVID-19. In this study, we performed systematic evolution of ligands by exponential enrichment and identified a novel RNA aptamer. This RNA aptamer not only bound to IL-6R with a dissociation constant of 200 n m, but also inhibited the interaction of IL-6R with IL-6.


Subject(s)
Aptamers, Nucleotide/therapeutic use , COVID-19 Drug Treatment , Cytokine Release Syndrome/drug therapy , Interleukin-6/antagonists & inhibitors , Receptors, Interleukin-6/antagonists & inhibitors , Aptamers, Nucleotide/chemistry , Base Sequence , COVID-19/complications , Cytokine Release Syndrome/etiology , DNA, Viral/drug effects , Humans , Interleukin-6/metabolism , Receptors, Interleukin-6/metabolism , SELEX Aptamer Technique
2.
Biochem Biophys Res Commun ; 535: 47-53, 2021 01 08.
Article in English | MEDLINE | ID: covidwho-978223

ABSTRACT

The interaction of the multifunctional cytokine interleukin (IL)-6 and its receptor (IL-6R) is involved in various diseases, including not only autoimmune diseases such as rheumatoid arthritis but also cancer and cytokine storms in coronavirus disease 2019 (COVID-19). In this study, systematic evolution of ligands by exponential enrichment (SELEX) against human IL-6R from mRNA-displayed unnatural peptide library ribosomally initiated and cyclized with m-(chloromethyl)benzoic acid (mClPh) incorporated by genetic code expansion (sense suppression) was performed using the PURE (Protein synthesis Using Recombinant Elements) system. A novel 13-mer unnatural mClPh-cyclized peptide that binds to the extracellular domain of IL-6R was discovered from an extremely diverse random peptide library. In vitro affinity maturation of IL-6R-binding unnatural mClPh-cyclized peptide from focused libraries was performed, identifying two IL-6R-binding unnatural mClPh-cyclized peptides by next-generation sequencing. Because cyclization can increase the protease resistance of peptides, novel IL-6R-binding mClPh-cyclized peptides discovered in this study have the potential to be used for a variety of research, therapeutic, and diagnostic applications involving IL-6/IL-6R signaling.


Subject(s)
Benzoic Acid/chemistry , Peptides/chemistry , Receptors, Interleukin-6/chemistry , Ribosomes/chemistry , Cyclization , Genetic Code , Humans , Peptide Library , RNA, Messenger , SELEX Aptamer Technique
SELECTION OF CITATIONS
SEARCH DETAIL