Molecular mechanisms of TDP-43 misfolding and pathology in amyotrophic lateral sclerosis

A Prasad, V Bharathi, V Sivalingam… - Frontiers in molecular …, 2019 - frontiersin.org
TAR DNA binding protein 43 (TDP-43) is a versatile RNA/DNA binding protein involved in
RNA-related metabolism. Hyper-phosphorylated and ubiquitinated TDP-43 deposits act as …

From prions to stress granules: defining the compositional features of prion-like domains that promote different types of assemblies

A Fomicheva, ED Ross - International journal of molecular sciences, 2021 - mdpi.com
Stress granules are ribonucleoprotein assemblies that form in response to cellular stress.
Many of the RNA-binding proteins found in stress granule proteomes contain prion-like …

Prion‐like proteins: from computational approaches to proteome‐wide analysis

M Gil‐Garcia, V Iglesias, I Pallarès, S Ventura - FEBS open bio, 2021 - Wiley Online Library
Prions are self‐perpetuating proteins able to switch between a soluble state and an
aggregated‐and‐transmissible conformation. These proteinaceous entities have been …

SGnn: a web server for the prediction of prion-like domains recruitment to stress granules upon heat stress

V Iglesias, J Santos, J Santos-Suárez… - Frontiers in Molecular …, 2021 - frontiersin.org
Proteins bearing prion-like domains (PrLDs) are essential players in stress granules (SG)
assembly. Analysis of data on heat stress-induced recruitment of yeast PrLDs to SG …

AMYCO: evaluation of mutational impact on prion-like proteins aggregation propensity

V Iglesias, O Conchillo-Sole, C Batlle, S Ventura - BMC bioinformatics, 2019 - Springer
Background Around 1% of human proteins are predicted to contain a disordered and low
complexity prion-like domain (PrLD). Mutations in PrLDs have been shown promote a …

In silico Characterization of Human Prion-Like Proteins: Beyond Neurological Diseases

V Iglesias, L Paladin, T Juan-Blanco, I Pallarès… - Frontiers in …, 2019 - frontiersin.org
Prion-like behavior has been in the spotlight since it was first associated with the onset of
mammalian neurodegenerative diseases. However, a growing body of evidence suggests …

Prion-like domain disease-causing mutations and misregulation of alternative splicing relevance in limb-girdle muscular dystrophy (LGMD) 1G

C Batlle, S Ventura - Neural Regeneration Research, 2020 - journals.lww.com
Human prion-like proteins often correspond to nucleic acid binding proteins, displaying both
globular domains and long intrinsically disordered regions (IDRs)(Harrison and Shorter …

Manipulating the aggregation activity of human prion-like proteins

SM Cascarina, KR Paul, ED Ross - Prion, 2017 - Taylor & Francis
Considerable advances in understanding the protein features favoring prion formation in
yeast have facilitated the development of effective yeast prion prediction algorithms. Here …

病毒样相关疾病的致病突变和可变剪接相关性的调控异常

C Batlle, S Ventura - 中国神经再生研究(英文版), 2020 - sjzsyj.com.cn
Human prion-like proteins often correspond to nucleic acid binding proteins, displaying both
globular domains and long intrinsically disordered regions (IDRs)(Harrison and Shorter …

[引用][C] AMORPHOUS AGGREGATION NUCLEATED BY LIQUID DROPLETS MIMICKS THE FORMATION OF PATHOLOGICAL ALS-LINKED INCLUSIONS

J VAN LINDT