Kirill Sechkar
@ksechkar.bsky.social
41 followers 70 following 51 posts
DPhil Engineering Science student at Oxford Uni. All opinions are my own, but the risk you take by reading them is yours Other soc. media: http://cosoc.com/KSechkar
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ksechkar.bsky.social
NEW PREPRINT! Do you think we can do better when characterising resource competition properties of gene circuit modules? If no, think again; if yes, you’re in for a pitch how exactly we can do that – automated culturing, cybergenetic control and all! 1/
doi.org/10.1101/2025...
ksechkar.bsky.social
So how can we reframe 'balancing innovation with safety'? Well, it's still vital to *innovate safely* and have robust regulation, but I'd say we also have the responsibility to *innovate FOR safety* - and this premise is baked into the idea of Engineering Biology itself 6/6
ksechkar.bsky.social
Identifying these behaviours, we can then design biosystems with robustness, safety and reliability in mind (e.g. that's what our ongoing @eebio.bsky.social
programme is all about). Innovative stuff, but hardly pitted against safety! 5/6
ksechkar.bsky.social
Using automatic culturing platforms, we work to characterise biotechnologies' behaviours as they're affected by factors like randomness, evolution or (my own area of interest) the sheer interconnectedness and complexity of living systems - so they won't catch us by surprise 4/6
ksechkar.bsky.social
I, for one, am doing a PhD supervised by Prof Harrison Steel at the Oxford Control Group. Just like EngBio's name would suggest, we approach problems in *biology* with principles from control *engineering* - which include precisely robustness, predictability and safety! 3/6
ksechkar.bsky.social
One common point in these discussions is the need to 'balance innovation with safety'. Fair! As mentioned in the debate, one mishap can tarnish the field's reputation for good, so robust regulation is vital. But why do we often frame innovation and safety as opposites? 2/6
ksechkar.bsky.social
Exciting times in UK EngBio governance!
-Debate on the House of Lords' EngBio report (we submitted evidence for that, wow!) shorturl.at/bJHUE
-New Science & Technology framework shorturl.at/cZkGG
-EngBio Aspirations Report shorturl.at/F9dj0
Won't post all my precious thoughts, but hope one is OK 1/6
Parliamentlive.tv
Lords Grand Committee
shorturl.at
Reposted by Kirill Sechkar
ksechkar.bsky.social
NEW PREPRINT! Do you think we can do better when characterising resource competition properties of gene circuit modules? If no, think again; if yes, you’re in for a pitch how exactly we can do that – automated culturing, cybergenetic control and all! 1/
doi.org/10.1101/2025...
ksechkar.bsky.social
Thanks to my supervisor Prof Harrison Steel , as well as to our collaborators from @eebio.bsky.social - Sara Brancato, Prof Lucia Marucci and Dr Ludovic Renson for advice. They’re also working on exciting applications of CBC right now, so watch them closely (what a time to be alive!) 9/9
ksechkar.bsky.social
For now, this is more of a pitch with an in silico proof-of-concept, but we discuss which developments in SynBio and control will help us apply this protocol in vivo. Briefly, advanced control algorithms + single-cell culturing + optogenetics = fun 8/
ksechkar.bsky.social
We successfully simulate our protocol using different models of various complexities (e.g. see results for a mechanistic resource-aware cell model in the pic below) – gives us reason to think it should work in (even more complex) real cells! 7/
ksechkar.bsky.social
From start to finish, our proposed method involves first establishing the probe’s properties, then using it to do CBC with the genetic module of interest. The results can then predict how any two characterised modules will compete for resources! 6/
ksechkar.bsky.social
Here, the module of interest’s output is its fluorescent gene expression, and the feedback input is e.g. chemical induction of another ‘probe’ genetic module competing with it for resources 5/
ksechkar.bsky.social
We suggest using control-based continuation (CBC), where a stabilising external feedback input drives a system through the entire range of its equilibria! 4/
ksechkar.bsky.social
To gauge resource demands, we often look at how modules compete for gene expression resources with constitutive fluorescent reporter genes. But there’s a problem: in multistable systems, constant resource competition may drive your system to just one steady state among many possible
ksechkar.bsky.social
NEW PREPRINT! Do you think we can do better when characterising resource competition properties of gene circuit modules? If no, think again; if yes, you’re in for a pitch how exactly we can do that – automated culturing, cybergenetic control and all! 1/
doi.org/10.1101/2025...
ksechkar.bsky.social
Hope I’ve gotten you interested enough to go and read our paper for details! And the best way I can conclude is by thanking the editors & reviewers, @Harrison_Steel for supervision and coauthorship, and @Andreas_Porse and other Steel Lab members for their great advice! 10/10
ksechkar.bsky.social
We also consider beneficial *native* gene mutations. For the same growth advantage, these are less prone to triggering the Punisher than synthetic gene loss, yielding better fitness. Clonal interference can thus help to hinder engineered cell populations’ function loss 9/10
ksechkar.bsky.social
How about transient reductions in burden due to uneven plasmid and cell cycle fluctuations? We can likewise model these to show that the Punisher is robust to such disturbances 8/10
ksechkar.bsky.social
Though the Punisher’s aimed at penalising mutations of genes burdening the cell primarily via resource competition, we also model metabolic burden. Turns out, our design can punish mutations of metabolically burdensome genes, too – just tune the chemical induction again! 7/10
ksechkar.bsky.social
What’s new since the preprint? We now simulate many more scenarios beyond those just showcasing the Punisher in action! Beyond just studying our circuit, we believe our approaches could generally come in handy for resource-aware modelling of single cells and populations 6/10
ksechkar.bsky.social
We also define a population model based on deterministic and stochastic simulations, directly linking physiological parameters of synthetic genes and circuit performance on a populational level. Our model shows the Punisher really is helpful in settings like bioreactors 5/10
ksechkar.bsky.social
Direct sensing of burden gives the Punisher an edge over extant designs (like co-expression of essential genes with synthetic genes of interest), which may accidentally encourage mutant cell growth through unintended responses 4/10
ksechkar.bsky.social
Thanks to a self-activating switch, the Punisher’s triggered by burden reduction (eg by mutations) and excises an essential gene. The switching threshold can be tuned by chemical induction, so it can be reused for many applications without any long & costly DNA engineering 3/10
ksechkar.bsky.social
Recapping our preprint: by competing for cellular resources, the synthetic genes make host cells burdened & slow-growing, so mutants that lose these genes outgrow useful cells in a population. But our ‘Punisher’ gene circuit can sense burden & hinder mutant cell growth 2/10