The original paper, which was mainly based on the temperature-dependent fluorescence of a mitochondria-targeting probe, was accompanied by a “Primer” (journals.plos.org/plosbiology/ar…) highlighting potential flaws and implications, a special sort-of-peer-review step by PLOS Biology.
This new awesome resource @naturemethods - nature.com/articles/s4159… - offers some intriguing orthogonal validation. This is a proteome-wide study of protein thermal stability across 13 organisms, conducted using a mass-spec-based approach.
By measuring soluble protein left after heating at various temperatures, the thermal stability (really, a combination of stability + solubility, as the authors are careful to point out) of every protein in a sample can be measured in parallel.
On top of lots of cool stuff (Role of disorder in stability! Bacterial proteomes evolving closer to the edge of stability!), they find that mitochondrial respiratory chain enzymes, but not all mitochondrial proteins in general, have very high melting temperatures.
Additionally, they measure respiration rates in permeabilized cells (to bypass requirement for heat-sensitive glucose transporters), and match the finding about enzyme activities measured in the original paper - mitochondrial enzymes are perfectly happy running at 45°+!
The new study concludes that this “support[s] the hypothesis that proteins of the respiratory chain may have evolutionarily adapted to higher local temperatures by increasing their thermal stability”
Which is the exact question raised by the Primer accompanying the original paper - “Whether the mitochondrial enzymes are genuinely optimised for close to 50°C or just operate faster at that temperature before they fall to pieces is not clear.”
So, in exploring the evolution of proteome stability in a super cool resource, we have some orthogonal evidence that mitochondrial respiratory chain proteins really are evolved for higher temperatures. Of course, that doesn’t mean they’re actually running at 50°C.
But it’s an intriguing bit of evidence, and increases the probability that the original “50° mitochondria” report was on to something. It’s still unproven, and worth thinking about other ways to approach further proving (or disproving) it, but a cool spin on the problem!
That’s just one cool conclusion from this study on the “meltome”. It’s an amazing paper and dataset to examine for anyone interested in evolution of proteomes, sequence determinants of biophysical properties, and life at varying temperatures. Give it a read!
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Here’s a thread on anti-interferon autoantibodies, viral infections, and human immunology. This is less a covid thread, and more an anti-covid thread, if anything…
Summary: anti-IFN auto-Abs may be reflective of chronic inflammation, and may pre-exist in vulnerable groups at high levels. Presence in severe covid cases may therefore reflect basal immune variation which impacts covid, rather than a special covid-specific phenomenon.
This is prompted based on the new Science paper on autoantibodies against Type I IFNs in severe covid patients (science.sciencemag.org/content/early/…). Basically, ~10% of severe covid patients had high titer anti-IFNa antibodies that were functionally neutralizing.
I'm grateful that others have put together resources like bit.ly/ANTIRACISMRESO…, which has helped me learn to be better. So You Want To Talk About Race by @IjeomaOluo and How To Be An Antiracist by @DrIbram have been amazing, and I'm looking forward to reading deeper.
I haven't seen a similar central resource for donations, but various recommendations led me to eji.org (Equal Justice initiative, focused on criminal justice reform and education), voterparticipation.org (get people registered to vote)...
Super neat story on how cellular quality control impacts the mutational landscape of proteins - beneficial mutations in DHFR during deep mutational scanning are totally altered dependent on cellular QC #Biophysics#Evolutionbiorxiv.org/content/10.110… Way to go! @KortemmeLab
In an initial DMS experiment on DHFR, there were a large number (25% of all sequences!) of advantageous mutations spread across the whole protein. Reintroduction of QC protein Lon reduced the number of advantageous mutants and lowered average benefit of those mutations
Changes in selection coefficient (the “advantageous-ness”) were most striking at hydrophobic/aromatic residues and buried residues - and these correlate with Tm changes of variants. So Lon seems to be imposing higher standards on DHFR, particularly for destabilizing core mutants
A couple interesting bits of preliminary data on Langerhans cells and the huLangerin mouse used to study them. Effects of developmental absence of LCs on keratinocytes and T cells, and huLangerin-YFP labels some neurons (check your Cre mice!) #Genetics#Immunology
First - effect of loss of LCs in the huLangerin-DTA mice - biorxiv.org/content/10.110…. Bulk RNA-seq showed changes in keratinocytes and dendritic epidermal T cells, including cell-type specific changes (e.g. loss of IL17 pathway in DETCs).
Unfortunately, underlying data (either gene expression tables or raw RNA-seq data) don’t currently seem available, but hopefully the authors get that up shortly. Will be interesting to look at and prompt some hypotheses about how LCs control homeostasis and development.
CYTOF analysis of human neutrophils - 7 populations with differing phagocytosis, ROS, and FACS-compatible surface marker phenotypes. Changes in distribution between healthy + melanoma patients. #Immunology#Cancer#Neutrophilsbiorxiv.org/content/10.110…
Circulating neutrophil precursors, aged neutrophils, and a few populations of mature and immature neutrophils. Melanoma stage correlates with loss of dominant N2 (mature, ROS++, lowly phagocytic), and increase of N5 (immature, non-proliferative, ROS+, lowly phagocytic).
Interesting to note the phagocytosis-SSC staining in Fig4A - big changes in SSC for some populations with zymosan, others not so much - degranulation, different phagosomes…? Similarly, bimodal peaks for ROS production in same populations…
Looking at malaria patients with thrombocytopenia shows decreased circulating IL-1 inversely correlating with platelet, but not total leukocyte, numbers, and depletion during PBMC prep almost eliminated IL-1 (and TNF) production in response to LPS!
This preprint also has very thorough evidence that platelets *do not* express inflammasomes or meaningfully contribute IL-1/18, and an exhaustive list of all the ways that platelets *don’t* stimulate myeloid inflammasome activation. Super solid work!