TY - JOUR
T1 - Tumor microenvironment–targeted PROTAC nanoparticle self-assembly broadly predicted by structural descriptors
AU - Vogt, Kristen C.
AU - Panagiotakopoulou, Magdalini
AU - Honu, Mandana T.Manzari
AU - Perea, Ana Marie
AU - Hu, Xiaoping
AU - Yu, Xufen
AU - Raziuddin, Raashed
AU - LaPlant, Quincey
AU - Ruiz, Stephen
AU - Raju, G. Praveen
AU - Jin, Jian
AU - Scheinberg, David A.
AU - Heller, Daniel A.
N1 - Publisher Copyright:
© 2025 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC ).
PY - 2025/12/5
Y1 - 2025/12/5
N2 - Proteolysis-targeting chimeras (PROTACs) are catalytic protein degraders with promising preclinical activity. The clinical translation of PROTACs has been limited by poor pharmacologic properties and toxicities, in part due to their “non-druglike” characteristics, including large molecular weights. We found that the vast majority of PROTACs can self-assemble into nanoparticles, yielding nanoparticle PROTACs (nanoPROTACs) with ultrahigh drug loadings. While PROTAC molecular features can be deleterious to their pharmacokinetic properties, we found that they can drive nanoencapsulation more efficiently than FDA-approved small-molecule drugs. Using structure-based prediction algorithms, we identified spatial autocorrelation molecular descriptors that defined nanoPROTAC formation with 96% sensitivity at 100% specificity. NanoPROTACs, targeted to the tumor microenvironment via P-selectin, led to significantly enhanced tumor drug uptake, target degradation, tumor growth inhibition, and overall survival in solid tumor xenografts. These findings offer a broad strategy to improve the pharmacologic properties and therapeutic index of PROTACs and potentially other non-druglike experimental therapeutics.
AB - Proteolysis-targeting chimeras (PROTACs) are catalytic protein degraders with promising preclinical activity. The clinical translation of PROTACs has been limited by poor pharmacologic properties and toxicities, in part due to their “non-druglike” characteristics, including large molecular weights. We found that the vast majority of PROTACs can self-assemble into nanoparticles, yielding nanoparticle PROTACs (nanoPROTACs) with ultrahigh drug loadings. While PROTAC molecular features can be deleterious to their pharmacokinetic properties, we found that they can drive nanoencapsulation more efficiently than FDA-approved small-molecule drugs. Using structure-based prediction algorithms, we identified spatial autocorrelation molecular descriptors that defined nanoPROTAC formation with 96% sensitivity at 100% specificity. NanoPROTACs, targeted to the tumor microenvironment via P-selectin, led to significantly enhanced tumor drug uptake, target degradation, tumor growth inhibition, and overall survival in solid tumor xenografts. These findings offer a broad strategy to improve the pharmacologic properties and therapeutic index of PROTACs and potentially other non-druglike experimental therapeutics.
UR - https://www.scopus.com/pages/publications/105024037024
U2 - 10.1126/sciadv.adu2292
DO - 10.1126/sciadv.adu2292
M3 - Article
C2 - 41348877
AN - SCOPUS:105024037024
SN - 2375-2548
VL - 11
JO - Science advances
JF - Science advances
IS - 49
M1 - eadu2292
ER -