
Decoding #mechanobiology at the cell-surface using structural and cellular biophysics. Protein-DNA conjugation via #HUHtags: https://xitter.cf/t.co/uflkydQZpS
University of Minnesota
Joined November 2015
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Wendy Gordon lab UMN retweeted
When we say sample to discovery, this is what we mean.
We send back results you can act on: volcano plots and pathway enrichment for RNA-Seq, species-level breakdowns for microbiome samples, annotated plasmid maps, and alignments that point you straight to the mismatch.
Explore them interactively, then download publication-ready figures for your next paper or lab meeting. 🦖
Wendy Gordon lab UMN retweeted
I always considered myself a well-rounded person. Then I got a PhD and became an expert on a topic that only 7 people understand. Four of them think I’m an idiot.
Wendy Gordon lab UMN retweeted
How strongly a CAR-T cell binds a cancer cell matters. 🔬 New @ASH_hematology research from @MarcoRuella and colleagues uses #CellAvidity to explore this connection and its impact on CAR T function.
Read more: ashpublications.org/blood/ar…
Wendy Gordon lab UMN retweeted
Current Affairs: Tissue flow creates mechanical cues to coordinate immune-cell migration during development
📹 Hoang Anh Le et al @mayor_lab UCL, London in @NatureCellBio
➡️ bpod.org.uk/archive/2026/9/3… with @AntDLewis
Wendy Gordon lab UMN retweeted
Four cancer cells displaying continuous membrane blebbing videoed through a DIC microscope. No, these cells are not dying. #CellBiology
Wendy Gordon lab UMN retweeted
kpiCells: biomimetic artificial cells for investigating mechanoregulation in cell-cell interactions.
nature.com/articles/s41592-0…
Wendy Gordon lab UMN retweeted
bunsen burners were never necessary
#MicrobiologyMonday: Bunsen burners are used to reduce airborne contamination. Data in #JournalSpectrum suggest the practice is not evidence-based and, except in some cases, Bunsen burners can be removed from practice w/o compromising research integrity. asm.social/33D
Wendy Gordon lab UMN retweeted
WHaloForce enables chemigenetic imaging of molecular tension in living cells and animals. A wonderful collaboration with Shaohe Wang at HHMI Janelia. biorxiv.org/content/10.64898…
Wendy Gordon lab UMN retweeted
📢 Check out our new paper in @acsnano, where we show that nanoscale architecture can control cellular signaling and behavior!
This work was led by our Project Scientist @Skottlee, in collaboration with the Padmini Rangamani Lab.
doi.org/10.1021/acsnano.6c03…
Wendy Gordon lab UMN retweeted
More atomic force microscopy videos. These show Cas9 "searching" through DNA and then cutting it.
It's surprising how long the DNA cut takes. It'd be cool to see similar videos for bridge recombinases.
These were published by the great @hnisimasu in 2017.
Wendy Gordon lab UMN retweeted
A bit belatedly sharing this beautiful work of carmina’s. A real tour de force of live imaging!
Direct observation of Notch signaling–induced transcription hubs mediating gene-expression responses | Science Advances science.org/doi/10.1126/scia…
Wendy Gordon lab UMN retweeted
First synthetic protein motor moves along DNA in controlled, programmable steps buff.ly/62glrBT
Wendy Gordon lab UMN retweeted
A belated re-post after a brief sci-media hiatus - congratulations to @connorjtou & the team!
We sought to overcome a key challenge for inserting large DNAs into the genome: toxicity & innate immune responses. 🧬 🚫
Our paper was published in @Nature: nature.com/articles/s41586-0…
Today in @Nature we introduce INSTALL, which bypasses mammalian DNA immune sensing to enable non-viral DNA integration with recombinases—a step toward safe, scalable, and mutation-agnostic genome editing. 🧬 🧵(1/13)
nature.com/articles/s41586-0…
@BKleinstiver @CGM_MGH @MassGeneralNews @harvardmed
Wendy Gordon lab UMN retweeted
Attention researchers in muscle biology, stem cell biology, neuromuscular disorders, and Notch signaling👇
doi.org/10.1172/JCI198639
Atsushi Asakura & team @UMNews report that Jag2 mutations impair the self-renewal, differentiation, and regeneration of myogenic stem cells through disrupted cis-inhibition and trans-activation of Notch signaling.
The image shows impaired skeletal #MuscleRegeneration in Jag2 mutant mice, as detected by hematoxylin and eosin (HE) staining. Image courtesy of Atsushi Asakura
#MuscularDystrophy
Wendy Gordon lab UMN retweeted
About 6.2 billion basepairs of DNA are 'packed' into the nucleus of each human cell. Scaled by a factor of 500,000x, this is akin to packing a 1,000-kilometer-long string (roughly the distance from New York City to Detroit) into a small bedroom.
How does all that DNA fit? Well, let’s do some back-of-the-envelope calculations:
The human genome is 6.2 billion basepairs in length, and each basepair is separated by 0.34 nanometers along the helix. (A carbon-carbon single bond is about half that length.) Multiply these numbers together, and we see that the DNA inside of each cell stretches about 2.1 meters in length. This is not a scaled value! A human cell nucleus has a diameter of about 6 micrometers.
So what fraction of that nucleus is 'occupied' by the DNA?
First, we calculate the volume of the cell nucleus. Given a radius of 3 micrometers, and using the regular equation (V = 4/3*pi*r^3), we get a volume of 113 cubic micrometers.
The DNA can be modeled as a cylinder. This cylinder is 2.1 meters long and about 2 nanometers in diameter. Again, using the equation for volume of a cylinder (V=π*r^2*h) we get 6.6 cubic micrometers.
In short: The human genome occupies about 6% of the cell nucleus. This is not tightly packed at all.
The main problem is that once you pack all of this 'string' into the nucleus, you have created a really difficult search problem for yourself. This string is coiled up tightly and, if you are an enzyme, then you might need to find a particular segment of the string located at, say, position 4,284,283,192. Good luck with that! And yet, cells have evolved highly effective search strategies to quickly retrieve information, which I think is one of the great innovations of evolution.
Wendy Gordon lab UMN retweeted
Genomic integration of DNA templates is made more precise through microhomology-focused design go.nature.com/41GoBiX
rdcu.be/fpOUC
Wendy Gordon lab UMN retweeted
New in @CellCellPress (Xiang Zhao group, SIBCB): #catchbonds strengthen under force and drive #TCR potency, but affinity assays miss them. The C-Trap measured them directly, enabling engineered TCRs that cleared tumors in vivo without off-target toxicity. This can be applied to other mechanosensory systems! Congrats to all the authors! 🎉
👉Read the publication: cell.com/cell/abstract/S0092…
Wendy Gordon lab UMN retweeted
Do you need a super active #CRISPR Cas for in vivo editing? I have not one, but two options for you. Activities rival SpyCas9, but they fit into an scAAV. Check out our latest paper, co-led by Fedor Gorbenko and Irene Sala. Just out in Genome Research. link.springer.com/article/10…



























