Enzymatic synthesis of defined-length poly(ADP-ribose) and the investigation of cell-permeable poly(ADP-ribose) glycohydrolase inhibitors

Yang, Woojin

Permalink

https://hdl.handle.net/2142/90688 Copy

Description

Title

Enzymatic synthesis of defined-length poly(ADP-ribose) and the investigation of cell-permeable poly(ADP-ribose) glycohydrolase inhibitors

Author(s)

Yang, Woojin

Issue Date

2016-04-28

Director of Research (if dissertation) or Advisor (if thesis)

Hergenrother, Paul J.

Department of Study

Chemistry

Discipline

Chemistry

Degree Granting Institution

University of Illinois at Urbana-Champaign

Degree Name

M.S.

Degree Level

Thesis

Keyword(s)

• PAR
• Poly(ADP-ribose) Glycohydrolase (PARG)

Abstract

Poly(ADP-ribosylation) (PARylation) is an important post-translational modification that maintains genomic stability in a cell. Engaging in important cellular processes such as DNA repair and cell death signaling, PARylation has gathered considerable interest as a target for genotoxic chemotherapy against cancer cells. To this end, various Poly(ADP-ribose) Polymerase (PARP) inhibitors have been developed to induce sensitivity to genotoxic stress in BRCA-mutated cancer cells, and Poly(ADP-ribose) Glycohydrolase (PARG) inhibition is investigated as an alternate pathway to PARP inhibition in genotoxic chemotherapy. However, little is known about the exact mode of interaction between PAR and different proteins mainly due to the fact that PARP produces polydisperse mixtures of PAR through a heterogeneous modification process. To tackle these problems, a controlled enzymatic synthesis pathway of PAR has been investigated through the use of masked β-NAD+ derivatives that can homogenously and monomerically modify PARP. In order to verify its ability to modify PARP, a sample of proparagyl-β-NAD+ derivative was used in an automodification assay with hTNKS-1. In addition, a PARG inhibitor prodrug in the form of an alanine-ester-masked ADP-HPM was developed as a cell-permeable PARG inhibitor to investigate its effect in a whole cell. In order to verify its activity, an in vitro experiment of the enzymatic cleavage of its masking group with HINT-1 was performed and the results were analyzed via LC/MS.

Graduation Semester

2016-05

Type of Resource

text

Permalink

http://hdl.handle.net/2142/90688

Copyright and License Information

Copyright 2016 Woojin Yang

Owning Collections