scholarly journals Structural proteomics and protein complexes – special issue

PROTEOMICS ◽  
2021 ◽  
Vol 21 (21-22) ◽  
pp. 2000286
Author(s):  
Helen J. Cooper ◽  
Aneika C. Leney
2006 ◽  
Vol 84 (3-4) ◽  
pp. 367-376 ◽  
Author(s):  
Christiane Rollenhagen ◽  
Nelly Panté

Uridine-rich small nuclear ribonucleoproteins (U snRNPs) are the building units of the spliceosome. These RNA and protein complexes assemble in the cytoplasm. After proper assembly and RNA maturation, mature U snRNPs are imported into the cell nucleus, where they take part in the splicing process. In this paper we review the current knowledge of how U snRNPs enter the nucleus.


2020 ◽  
Vol 25 (9) ◽  
pp. 945-946
Author(s):  
Pascal Albanese ◽  
Sem Tamara ◽  
Richard A. Scheltema ◽  
Cristina Pagliano

2020 ◽  
Vol 118 (3) ◽  
pp. 291a
Author(s):  
Chi-Min Ho ◽  
Xiaorun Li ◽  
Mason Lai ◽  
Thomas Terwilliger ◽  
Josh Beck ◽  
...  

2019 ◽  
Vol 17 (1) ◽  
pp. 79-85 ◽  
Author(s):  
Chi-Min Ho ◽  
Xiaorun Li ◽  
Mason Lai ◽  
Thomas C. Terwilliger ◽  
Josh R. Beck ◽  
...  

2003 ◽  
Vol 25 (1) ◽  
pp. 7-9
Author(s):  
Hannes Ponstingl ◽  
Janet M. Thornton

Recent advances in protein separation technology and mass spectrometry (MS) have enabled the systematic identification and quantification of large sets of proteins from an organelle, cell type or organism. In principle, protein isoforms, enzymically modified variants and protein complexes can be studied, for instance, at a certain stage in development or in response to stress or more subtle changes of the environment. An important pre-clinical application is the search for protein markers in body fluids for diagnostic purposes. Such proteomics studies can be performed increasingly at high-throughput rates that are reminiscent of those of genomic sequencing or the monitoring of messenger RNA levels. Thus, large sets of proteins can be monitored simultaneously in a single experiment. Proteomics data will increasingly be followed up by investigations of the three-dimensional structures of proteins and protein complexes at atomic detail in large-scale structural proteomics projects. We attempt in this article to give a flavour of what to us seem important experimental developments and to point to links with bioinformatics resources where appropriate.


2021 ◽  
Vol 22 (6) ◽  
pp. 3008
Author(s):  
Young-Su Yi ◽  
Miyong Yun

Inflammation is an innate immunity protecting the body from pathogens and cellular damages and comprises two steps; 1) priming (preparatory step) and triggering (activation step). The key feature of the triggering step is the activation of inflammasomes that are intracellular protein complexes consisting of pattern recognition receptors and inflammatory molecules. Inflammasomes are activated in response to various ligands, leading to the caspase-1-mediated maturation and secretion of pro-inflammatory cytokines, IL-1β and IL-18 and the gasdermin D-mediated pyroptosis, an inflammatory form of cell death. Previous studies have demonstrated that inflammasome activation is a key determinant of inflammatory responses and many human diseases; therefore, inflammasomes have been attracted much attention as critical drug targets to prevent and treat various human diseases.


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