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Review
. 2024 Mar 4;13(5):449.
doi: 10.3390/cells13050449.

Proximity-Induced Pharmacology for Amyloid-Related Diseases

Affiliations
Review

Proximity-Induced Pharmacology for Amyloid-Related Diseases

Andrea Bertran-Mostazo et al. Cells. .

Abstract

Proximity-induced pharmacology (PIP) for amyloid-related diseases is a cutting-edge approach to treating conditions such as Alzheimer's disease and other forms of dementia. By bringing small molecules close to amyloid-related proteins, these molecules can induce a plethora of effects that can break down pathogenic proteins and reduce the buildup of plaques. One of the most promising aspects of this drug discovery modality is that it can be used to target specific types of amyloid proteins, such as the beta-amyloid protein that is commonly associated with Alzheimer's disease. This level of specificity could allow for more targeted and effective treatments. With ongoing research and development, it is hoped that these treatments can be refined and optimized to provide even greater benefits to patients. As our understanding of the underlying mechanisms of these diseases continues to grow, proximity-induced pharmacology treatments may become an increasingly important tool in the fight against dementia and other related conditions.

Keywords: PROTACs; amyloid-related diseases; conformational diseases; drug discovery; neurodegenerative diseases; proximity-induced pharmacology.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
(A) Natural pathway of ubiquitin–proteasome system controlling protein degradation and turnover. (B). PROTAC-mediated degradation of the protein of interest (POI) by the ubiquitin–proteasome system.
Figure 2
Figure 2
Chemical structures of described PROTACs and SNIPERs.

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