Edward Wallace

@ewjwallace.bsky.social

Group leader, RNA and cellular adaptation in fungi. Carpentries data science instructor. Trying to make my corner of science a better place. Opinions my own. https://ewallace.github.io

Where are we at on acceptable abbreviations for fluorescent proteins? Like, GFP for green fluorescent protein sure, but is mNG for mNeonGreen too much? Etc? Your strongest opinions and arguments invited.

I worked for UKRI for seven years and in my experience, the short timescales were 100% because of delays in central government. Usually because of delays in sign off by a minister; in the worst cases, due to number 10 comms teams insisting we hold back so the PM could announce it or whatever. 1/3

Kirsty Grainger @kirstygrainger.bsky.social · 2mo ago

A new TOP FIVE has just dropped. The @ukri.org TOP FIVE shortest timescales from call opening to closing. And you won't believe the winner 👀

How do fungi grow directionally? We think part of the mechanism involves local translation of mRNA near the tip, especially of cell wall components. Delighted to share our preprint showing that an RNA-binding protein, SsdA/Ssd1, is trafficked to the tip of growing fungal filaments.

Domenico Modaffari@dmodaffari.bsky.social · 3mo ago

Happy to share that the bulk of my PhD work is now on bioRxiv! We followed SsdA, the A. nidulans ortholog of yeast RNA-binding protein Ssd1, and found it forms motile mRNP puncta in hyphae. [1/7] www.biorxiv.org/content/10.6...

I am learning a lot from this debate about the last eukaryotic common ancestor. It's thought-provoking to have competing hypotheses and perspectives argued out there in the open. Here, the two arguments are internally consistent, yet different conclusions... so where's the wrong assumption?

Bungo Akiyoshi@bungoakiyoshi.bsky.social · 6mo ago

I appreciate the comments by Max Raas, Eelco Tromer and others on my paper published last year "Hypothesis that ancestral eukaryotes sexually proliferated without kinetochores or mitosis". However, I do not think their critiques can reject my hypothesis. For details, please read the paper. 1/n

Wonderful talk by the legendary Jane Richardson today on validation of #cryoEM and #xray protein structures as part of the S2C2 modeling and validation workshop at SLAC. I continue to be amazed by how deeply she understands macromolecular geometry.

Jane Richardson stands next to the lectern and in front of the title slide of her talk. 30 October, 2025. Slide with the follow text: “The zen of model anomalies. Correct most of them. Treasure the meaningful valid few. Live serenely with the rest!”

I NEED to tell you the story of Tae Heung “William” Kim. He's a graduate student at Texas A&M where he's working on a vaccine for Lyme disease. He's a *legal permanent resident* of the United States. And he's been in ICE detention for 12 days & counting, transferred Tuesday to South Texas.

From left to right, Dr. Albert Mulenga, William Tae Heung Kim, Dr. Thu Thuy Nguyen, Dr. Alex Kiarie Gaithuma, Dr Hassan Hakimi and Emily Bencosme Cuevas. Kim is a Texas A&M researcher who was detained in San Francisco last Monday despite being a permanent resident of the United States and a green card holder.

COURTESY OF TEXAS A&M UNIVERSITY

It’s actually even worse: they show it as a gel, which is pure fluorescence units, but a BioAnalyzes records as the molecules pass a single point sensor and critically _fails to normalize for different molecule speeds_ This results in a near-logarithmic overcounting of large molecules!

Tami Lieberman@contaminatedsci.bsky.social · last yr.

This is your regular reminder that the BioAnalyzer/TapeStation reports fluorescence units, not # of molecules. Left is bioA trace, and right is fragment size calculated from either read output (blue) or transformation of BioA trace (black). Fig 3 from journals.plos.org/plosone/arti...