Zunlong Ke

@zunlongke.bsky.social

Assistant Professor @UT Austin | Structural Virology | cryo-EM and cryo-ET | Postdoc with John Briggs @MRC_LMB @MPI_biochem | PhD with Elizabeth Wright @GeorgiaTech @Emory

Inspired by Utz, I ported the old Briggs lab tools to ChimeraX in a single bundle named Geopickr, with some extra utilities (geopicking on morphometrics surfaces!). I've submitted it to the toolshed, but in the meantime: github.com/baradlab/Geo...

Geopickr enables particle picking on surfaces, spheres, tubes, and filaments interactively in ChimeraX!
Utz Ermel@uermel.bsky.social · 2mo ago

Claude Code is pretty good at writing ChimeraX plugins! This one is almost entirely good context and some prompting: github.com/uermel/chime... Most likely older plugins could be ported over that way relatively easily.

Cryo-ET gives unparalleled views of cellular structures, but targeted sample preparation by cryo-FIB milling has been a constraint. No longer! A new workflow yields close to 100% targeting success for centrioles & other small structures. Read the preprint ⤵️ www.biorxiv.org/content/10.6...

Diagram of FIB-SEM with integrated fluorescence microscope alongside cryo lamella micrograph and 3D segmentation highlighting targeted centrioles

Academic writing should be addressed neither to the public nor to other academics. It should be addressed to a single interlocutor with whom you have a petty rivalry and whose work you are trying to discredit

Important new results from lab alumnus Hui Guo @mydange.bsky.social, now a postdoc in the @briggsgroup.bsky.social, out on bioRxiv.

Ed Hutchinson@socialinfluenza.bsky.social · 3mo ago

Absolutely extraordinary work from Hui Gao, John Briggs and co @mpibiochem.bsky.social on the structure of the influenza matrix protein in situ, particularly in filamentous virions. It's beautiful, and answers questions I've been wondering about for twenty years www.biorxiv.org/content/10.6...

A reconstruction of part of the M1 helix of influenza A virus (looking from the outside of the virion, down onto the top of the N terminal domain of M1), showing a helix of M1 protomers (blue) bound to phosphatidyl inositol (green), and a 'seam' of M1 protomers placed every fourth unit in a distinct conformation (pink) which allows them to bind to the C-terminal domains of the NA tetramer (yellow).
J