Polymers for Disrupting Protein-Protein Interactions: Where Are We and Where Should We Be?

被引:2
作者
Le, Stephanie P. [1 ,2 ]
Krishna, Jithu [1 ,2 ]
Gupta, Prachi [1 ,2 ]
Dutta, Ranit [1 ,2 ]
Li, Shanlong [1 ,2 ]
Chen, Jianhan [1 ]
Thayumanavan, S. [1 ,2 ,3 ]
机构
[1] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
[2] Univ Massachusetts, Inst Appl Life Sci, Ctr Bioact Delivery, Amherst, MA 01003 USA
[3] Univ Massachusetts, Dept Biomed Engn, Amherst, MA 01003 USA
基金
美国国家卫生研究院;
关键词
INTRINSICALLY DISORDERED PROTEINS; DER-WAALS INTERACTIONS; HOT-SPOTS; LIGHT-SCATTERING; SERUM-ALBUMIN; ELECTROSTATIC INTERACTION; HOFMEISTER-SERIES; THERMAL-STABILITY; AMMONIUM-SULFATE; BINDING-ENERGY;
D O I
10.1021/acs.biomac.4c00850
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein-protein interactions (PPIs) are central to the cellular signaling and regulatory networks that underlie many physiological and pathophysiological processes. It is challenging to target PPIs using traditional small molecule or peptide-based approaches due to the frequent lack of well-defined binding pockets at the large and flat PPI interfaces. Synthetic polymers offer an opportunity to circumvent these challenges by providing unparalleled flexibility in tuning their physiochemical properties to achieve the desired binding properties. In this review, we summarize the current state of the field pertaining to polymer-protein interactions in solution, highlighting various polyelectrolyte systems, their tunable parameters, and their characterization. We provide an outlook on how these architectures can be improved by incorporating sequence control, foldability, and machine learning to mimic proteins at every structural level. Advances in these directions will enable the design of more specific protein-binding polymers and provide an effective strategy for targeting dynamic proteins, such as intrinsically disordered proteins.
引用
收藏
页码:6229 / 6249
页数:21
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