Unknown

Dataset Information

0

Cyclic Peptidic Mimetics of Apollo Peptides Targeting Telomeric Repeat Binding Factor 2 (TRF2) and Apollo Interaction.


ABSTRACT: Telomeric repeat binding factor 2 (TRF2) is a telomere-associated protein that plays an important role in the formation of the 3' single strand DNA overhang and the "T loop", two structures critical for the stability of the telomeres. Apollo is a 5'-exonuclease recruited by TRF2 to the telomere and contributes to the formation of the 3' single strand DNA overhang. Knocking down of Apollo can induce DNA damage response similar to that caused by the knocking down of TRF2. In this Letter, we report the design and synthesis of a class of cyclic peptidic mimetics of the TRFH binding motif of Apollo (ApolloTBM). We found conformational control of the C terminal residues of ApolloTBM can effectively improve the binding affinity. We have obtained a crystal structure of a cyclic peptidic Apollo peptide mimetic (34) complexed with TRF2, which provides valuable guidance to the future design of TRF2 inhibitors.

SUBMITTER: Chen X 

PROVIDER: S-EPMC5949732 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Cyclic Peptidic Mimetics of Apollo Peptides Targeting Telomeric Repeat Binding Factor 2 (TRF2) and Apollo Interaction.

Chen Xia X   Liu Liu L   Chen Yong Y   Yang Yuting Y   Yang Chao-Yie CY   Guo Tianyue T   Lei Ming M   Sun Haiying H   Wang Shaomeng S  

ACS medicinal chemistry letters 20180425 5


Telomeric repeat binding factor 2 (TRF2) is a telomere-associated protein that plays an important role in the formation of the 3' single strand DNA overhang and the "T loop", two structures critical for the stability of the telomeres. Apollo is a 5'-exonuclease recruited by TRF2 to the telomere and contributes to the formation of the 3' single strand DNA overhang. Knocking down of Apollo can induce DNA damage response similar to that caused by the knocking down of TRF2. In this Letter, we report  ...[more]

Similar Datasets

| S-EPMC6393293 | biostudies-literature
2018-12-16 | GSE117214 | GEO
| S-EPMC7611063 | biostudies-literature
2018-12-17 | PXD010672 | Pride
2018-12-16 | GSE117212 | GEO
| S-EPMC2666026 | biostudies-literature
| S-EPMC544002 | biostudies-literature
| S-EPMC4357705 | biostudies-literature
2018-12-16 | GSE117213 | GEO