The known unknowns of the Hsp90 chaperone
원문 초록
Molecular chaperones are vital proteins that maintain protein homeostasis by assisting in protein folding, activation, degradation, and stress protection. Among them, heat-shock protein 90 (Hsp90) stands out as an essential proteostasis hub in eukaryotes, chaperoning hundreds of "clients" (substrates). After decades of research, several "known unknowns" about the molecular function of Hsp90 remain unanswered, hampering rational drug design for the treatment of cancers, neurodegenerative and other diseases. We highlight three fundamental open questions, reviewing the current state of the field for each, and discuss new opportunities, including single-molecule technologies, to answer the known unknowns of the Hsp90 chaperone.
함께 살펴볼 논문
공통 태그를 근거로 연결했습니다. 실제 인용 관계나 논문의 우수성을 뜻하지 않습니다.
Lattice Protein Folding with Variational Annealing
Molecular Diffusion Models with Virtual Receptors
Computational Explorations in Biomedicine: Unraveling Molecular Dynamics for Cancer, Drug Delivery, and Biomolecular Insights using LAMMPS Simulations
Assay2Mol: large language model-based drug design using BioAssay context
TABASCO: A Fast, Simplified Model for Molecular Generation with Improved Physical Quality
CovDocker: Benchmarking Covalent Drug Design with Tasks, Datasets, and Solutions
토론
이 논문과 연결된 포럼 글이 아직 없습니다.