Abstract Protein disulphide formation between cysteine residues impacts protein folding and function, yet the context in which it occurs often determines whether it is beneficial or detrimental. To ensure proper disulphide status, organisms have evolved compartment-specific disulphide maintenance systems. Some of these...
J. D. West· Philosophical transactions o...· 0 citations
COS plasma membrane acts as a shunt conducting free transmembrane proteins between lamellae by Brownian diffusion, even in the presence of crowding effects and complex membrane geometry, while lamellae are capacitive sources/sinks.
A. Tokarev, Peter D. Calvert· Biophysical Journal· 0 citations
This work provides the first systematic comparison of MRM, MS3, and in-source CID for PPG quantification, establishing a sensitive analytical platform with complementary greenness and practical applicability assessments using AGREE, AGSA, CACI, and GEMAM, for polymer bioanalysis in complex matrices.
Jia-Rui Zhang, Zi-Chan Tian, Jin-Qing Wu et al.· In Analysis· 0 citations
High-resolution structure determination of RNA remains a major challenge due to its conformational flexibility, intrinsic heterogeneity, and susceptibility to degradation. Although RNA plays central roles in gene regulation, viral replication, and cellular homeostasis, RNA-only structures represent a small fraction of...
Jerricho Tipo, K. Gottipati, Marc C. Morais et al.· Journal of Biological Chemis...· 0 citations
Reach audiences
Advertise in front of researchers, engineers, and readers.
Haplo-identical hematopoietic cell transplantation (haploHCT) is an integral treatment paradigm for patients with leukemia. While overall survival (OS) post-haploHCT has steadily improved, relapse-free survival (RFS) remains relatively stagnant. Upon the discovery of killer immunoglobulin-like receptors (KIRs) on natur...
S. Gottschalk, Ying Li, S. Selukar et al.· Blood Advances· 0 citations
Abstract Disruption of protein homoeostasis, or proteostasis, is a hallmark of protein conformational diseases (PCDs), including Alzheimer's and Parkinson's disease. These disorders are characterized by progressive protein aggregation and cellular dysfunction, yet no effective therapies exist. Emerging evidence indicat...
Daniel M. Czyż, Brittani M. Brown· Philosophical transactions o...· 0 citations
Abstract Proteostasis, the process governing the dynamic regulation of protein synthesis, folding and degradation, is critical for maintaining cell function and organismal health. Ageing disrupts this intricate system, leading to inactive, misfolded and/or aggregated proteins that contribute to age-associated pathologi...
Neethu Babu, Katie L. Whalen, Brian Freeman· Philosophical transactions o...· 1 citation
Bruton tyrosine kinase (BTK) and BCL2 are key therapeutic targets in marginal zone lymphoma (MZL). We evaluated the novel BTK degrader tacabrutideg (BGB-16673) and the secondgeneration BCL2 inhibitor sonrotoclax, alone and in combination, in MZL models, including derivatives with acquired resistance to BTK, BCL2, and P...
A. Arribas, Alex Zadro, E. Civanelli et al.· Haematologica· 0 citations
Fructose-1,6-bisphosphatase (FBPase) deficiency is a rare autosomal recessive disorder of gluconeogenesis caused by the biallelic pathogenic variants of FBP1. Recurrent episodes of hypoglycemia and lactic acidosis usually occur during childhood. Because the ketone levels during hypoglycemic attacks may vary in patients...
Ikki Sakuma, Gerald I. Shulman, Tomoaki Tanaka· Endocrine journal· 0 citations
Abstract The mitochondrial chaperone and co-chaperone HSP60/HSP10 (HSPD1/ HSPE1), the mammalian homologues of bacterial GroEL/GroES, form a barrel-and-lid complex to fold newly imported or misfolded mitochondrial proteins. Several lines of evidence suggest that HSPD1 and HSPE1 have diverged in function. HSPD1 and HSPE1...
BACKGROUND
Glioblastoma (GBM) is the most aggressive form of primary brain cancer. Blood platelets have emerged as biomarkers where their RNA expression pattern indicates a tumor's presence. Our study aimed to characterize these patterns to identify biological processes associated with GBM and to evaluate their potenti...
Anna Giczewska, K. Pastuszak, L. van Hout et al.· Cancer Reports· 0 citations
Abstract Huntington's disease is caused by the trinucleotide repeat CAG expansion in the huntingtin gene, resulting in an N-terminal polyglutamine (polyQ) tract that renders the huntingtin protein (HTT) prone to misfolding and aggregation. Although polyQ expansion is an intrinsic driver of aggregation, the folding traj...
A new machine-learning framework aims to improve the success rate of computational protein design while moving away from results that reproduce sequences found in nature.