10 research outputs found
Cleavage-Resistant Protein Labeling With Hydrophilic Trityl Enables Distance Measurements In-Cell
Sequestration of Proteins in Stress Granules Relies on the In-Cell but Not the <i>In Vitro</i> Folding Stability
Sequestration of Proteins in Stress Granules Relies on the In-Cell but Not the <i>In Vitro</i> Folding Stability
Stress granules (SGs)
are among the most studied membraneless organelles
that form upon heat stress (HS) to sequester unfolded, misfolded,
or aggregated protein, supporting protein quality control (PQC) clearance.
The folding states that are primarily associated with SGs, as well
as the function of the phase separated environment in adjusting the
energy landscapes, remain unknown. Here, we investigate the association
of superoxide dismutase 1 (SOD1) proteins with different folding stabilities
and aggregation propensities with condensates in cells, in
vitro and by simulation. We find that irrespective of aggregation
the folding stability determines the association of SOD1 with SGs
in cells. In vitro and in silico experiments however suggest that the increased flexibility of the
unfolded state constitutes only a minor driving force to associate
with the dynamic biomolecular network of the condensate. Specific
protein–protein interactions in the cytoplasm in comparison
to SGs determine the partitioning of folding states between the respective
phases during HS
Amyloid Oligomers: A Joint Experimental/Computational Perspective on Alzheimer's Disease, Parkinson's Disease, Type II Diabetes, and Amyotrophic Lateral Sclerosis
Protein misfolding and aggregation is observed in many amyloidogenic diseases affecting either the central nervous system or a variety of peripheral tissues. Structural and dynamic characterization of all species along the pathways from monomers to fibrils is challenging by experimental and computational means because they involve intrinsically disordered proteins in most diseases. Yet understanding how amyloid species become toxic is the challenge in developing a treatment for these diseases. Here we review what computer, in vitro, in vivo, and pharmacological experiments tell us about the accumulation and deposition of the oligomers of the (Aβ, tau), α-synuclein, IAPP, and superoxide dismutase 1 proteins, which have been the mainstream concept underlying Alzheimer's disease (AD), Parkinson's disease (PD), type II diabetes (T2D), and amyotrophic lateral sclerosis (ALS) research, respectively, for many years
Centimetre-scale micropore alignment in oriented polycrystalline metal–organic framework films via heteroepitaxial growth
Single Molecule 3D Orientation in Time and Space: A 6D Dynamic Study on Fluorescently Labeled Lipid Membranes
Accurate Determination of the Orientational Distribution of a Fluorescent Molecule in a Phospholipid Membrane
Dissipative particle dynamics simulations of polyelectrolyte self-assemblies. Methods with explicit electrostatics
Global, Regional, and National Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life-Years for 29 Cancer Groups, 1990 to 2016 A Systematic Analysis for the Global Burden of Disease Study
Fitzmaurice C, Akinyemiju TF, Al Lami FH, et al. Global, Regional, and National Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life-Years for 29 Cancer Groups, 1990 to 2016 A Systematic Analysis for the Global Burden of Disease Study. JAMA Oncology . 2018;4(11):1553-1568.IMPORTANCE The increasing burden due to cancer and other noncommunicable diseases poses a threat to human development, which has resulted in global political commitments reflected in the Sustainable Development Goals as well as the World Health Organization (WHO) Global Action Plan on Non-Communicable Diseases. To determine if these commitments have resulted in improved cancer control, quantitative assessments of the cancer burden are required. OBJECTIVE To assess the burden for 29 cancer groups over time to provide a framework for policy discussion, resource allocation, and research focus. EVIDENCE REVIEW Cancer incidence, mortality, years lived with disability, years of life lost, and disability-adjusted life-years (DALYs) were evaluated for 195 countries and territories by age and sex using the Global Burden of Disease study estimation methods. Levels and trends were analyzed over time, as well as by the Sociodemographic Index (SDI). Changes in incident cases were categorized by changes due to epidemiological vs demographic transition. FINDINGS In 2016, there were 17.2 million cancer cases worldwide and 8.9 million deaths. Cancer cases increased by 28% between 2006 and 2016. The smallest increase was seen in high SDI countries. Globally, population aging contributed 17%; population growth, 12%; and changes in age-specific rates, -1% to this change. The most common incident cancer globally for men was prostate cancer (1.4 million cases). The leading cause of cancer deaths and DALYs was tracheal, bronchus, and lung cancer (1.2 million deaths and 25.4 million DALYs). For women, the most common incident cancer and the leading cause of cancer deaths and DALYs was breast cancer (1.7 million incident cases, 535 000 deaths, and 14.9 million DALYs). In 2016, cancer caused 213.2 million DALYs globally for both sexes combined. Between 2006 and 2016, the average annual age-standardized incidence rates for all cancers combined increased in 130 of 195 countries or territories, and the average annual age-standardized death rates decreased within that timeframe in 143 of 195 countries or territories. CONCLUSIONS AND RELEVANCE Large disparities exist between countries in cancer incidence, deaths, and associated disability. Scaling up cancer prevention and ensuring universal access to cancer care are required for health equity and to fulfill the global commitments for noncommunicable disease and cancer control
