Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. Breaking the Fourth Wall: Modulating Quaternary Associations for Protein Regulation and Drug Discovery
 
review article

Breaking the Fourth Wall: Modulating Quaternary Associations for Protein Regulation and Drug Discovery

Long, Marcus J. C.
•
Hnedzko, Dziyana
•
Kim, Bo Kyoung
Show more
May 2, 2019
Chembiochem

Protein-protein interactions (PPIs) are an effective means to orchestrate intricate biological processes required to sustain life. Approximately 650000 PPIs underlie the human interactome; thus underscoring its complexity and the manifold signaling outputs altered in response to changes in specific PPIs. This minireview illustrates the growing arsenal of PPI assemblies and offers insights into how these varied PPI regulatory modalities are relevant to customized drug discovery, with a focus on cancer. First, known and emerging PPIs and PPI-targeted drugs of both natural and synthetic origin are categorized. Building on these discussions, the merits of PPI-guided therapeutics over traditional drug design are discussed. Finally, a compare-and-contrast section for different PPI blockers, with gain-of-function PPI interventions, such as PROTACS, is provided.

  • Details
  • Metrics
Type
review article
DOI
10.1002/cbic.201800716
Web of Science ID

WOS:000471317500001

Author(s)
Long, Marcus J. C.
•
Hnedzko, Dziyana
•
Kim, Bo Kyoung
•
Aye, Yimon  
Date Issued

2019-05-02

Publisher

WILEY-V C H VERLAG GMBH

Published in
Chembiochem
Volume

20

Issue

9

Start page

1091

End page

1104

Subjects

Biochemistry & Molecular Biology

•

Chemistry, Medicinal

•

Biochemistry & Molecular Biology

•

Pharmacology & Pharmacy

•

cancer

•

drug design

•

inhibitors

•

protein-protein interactions

•

quaternary associations

•

human ribonucleotide reductase

•

small-molecule inhibitors

•

structural basis

•

glycolytic-enzymes

•

targeting bcl2

•

binding-sites

•

cell-cycle

•

venetoclax

•

resistance

•

kinase

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LEAGO  
Available on Infoscience
June 28, 2019
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/158612
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés