Scientek retweeted
How to choose a reliable aptamer for biosensor development? We put our perspective of this problem in an article in @ACS_Sensors. The first step is to go back to the original SELEX paper and the last step is to do in-house validation. pubs.acs.org/ascefj/article-…
Scientek retweeted
📈 HIGHLY CITED | Influential research attracting global attention
📌 Aptamer-Based Smart Targeting and Spatial Trigger–Response Drug-Delivery Systems for Anticancer Therapy
🔗 mdpi.com/2227-9059/12/1/187
#HighlyCited #ResearchImpact
Scientek retweeted
Being mean is bad for your health.
A single hostile interaction:
+ locks you in a cortisol penalty box for 60-90 min
+ suppresses recovery capacity
+ elevates your heart rate
Kindness conserves your energy resources.
Scientek retweeted
Call for papers for a Molecular Therapy Nucleic Acids special issue on innovations in aptamer technology: advancements and applications. Submissions are invited by September 30, 2026.
hubs.li/Q04p7dxz0
@MolTherapy @asgctherapy
Scientek retweeted
Construction of an aptamer-conjuncted molecular artificial enzyme with enhanced activity and selectivity ift.tt/tk9iO5z
Scientek retweeted
'Time-Gated Fluorescent Aptamer Sensors Eliminate Autofluorescence during Continuous Molecular Detection in Complex Biological Matrices' from ACS Sensors is currently free to read as an #ACSEditorsChoice.
📖 Read the article: go.acs.org/ecY
Scientek retweeted
📣Call for Reading:
#Systematic_Review
Trends and Challenges of SPR Aptasensors in Viral Diagnostics: A Systematic Review and Meta-Analysis
By Elba Mauriz
mdpi.com/2079-6374/15/4/245
#SPR #biosensor #aptamer #aptasensor #open_access
Scientek retweeted
Aptamer charge-amplified field-effect transistor biosensors achieve picomolar detection limits for small-molecule biomarkers in complex biological matrices
ift.tt/dC3DpY2
#biorxiv_bioE
Scientek retweeted
i come from a programming background, so i didn’t have strong physics/engineering mental models for biology
inspired by the Quant Bible from MIT, i created an equivalent for engineering in biology
it’s not deep but has been helpful for me
link: drive.google.com/file/d/1Ye4…
Demis Hassabis just described what might be the end of genetic disease.
Google DeepMind built a system called AlphaGenome. It reads human DNA the way a software engineer reads source code.
Every letter. Every position. Every mutation across 3 billion characters.
Hassabis: “AlphaGenome is the best system in the world for predicting if a mutation will cause disease or if it’s benign.”
98% of your genome doesn’t code for proteins. For decades scientists treated it like dark matter. Present everywhere. Readable nowhere.
AlphaGenome reads it.
Now pair that with CRISPR. Jennifer Doudna’s gene editing tool can already target any DNA sequence on command.
The bottleneck was never the scalpel. It was knowing exactly where to cut.
Hassabis: “A combination of things like AlphaGenome and CRISPR could be incredibly powerful.”
That might be the most restrained sentence ever spoken about the future of medicine.
AI locates the exact mutation killing you. CRISPR goes in and deletes it. Not treatment. Not management. Deletion.
The hardest cases are multigenic. Mutations that cascade and compound. Hiding behind each other. Too complex for any human mind to untangle in a single lifetime.
Hassabis: “Those are even harder to detect, but actually perfect for AI to try and help with.”
The diseases that have defeated medicine for centuries are the exact ones AI is purpose-built to solve. That’s not a coincidence. That’s the turning point.
Every parent who sat in a white room and heard “there’s nothing more we can do.”
Every patient who watched their own biology turn against them with nothing to fight back.
Every name carved into stone because we could name the disease but couldn’t disarm it.
That era now has an expiration date.
Humanity spent 10,000 years fighting disease with observation and guesswork. We’re about to fight it with comprehension.
Your grandchildren may read about genetic disease the way you read about smallpox. As something that once ended millions of lives before we learned to read the code that wrote them.
Somewhere right now a child carries a death sentence folded into their DNA. Born with it before they ever opened their eyes. They don’t know it yet. Their parents don’t know it yet.
But for the first time in human history, the answer might arrive before the disease does.
That’s not technology. That’s the moment our biology stopped being our fate.
Scientek retweeted
Probably Craig Venters last interview.
The people who drone on about the necessity of NIH “basic science” are the duds and dropouts of the class.
It’s food stamps for the underachievers.
Scientek retweeted
you have no idea how much better it's getting in 2026
- peptides are viral and legal
- humans are being gene edited
- genomes are getting sequenced on kitchen tables
- psychedelics just got a presidential executive order
- cellular age reversal just entered human trials for the first time
- embryo selection for IQ is a commercial product you can buy today
- pig kidneys with 69 gene edits are keeping humans off dialysis
- AI is designing and validating drugs without human researchers in the loop
but somehow the society will not accept the science
Scientek retweeted
To all scientists immigrants: This is an amazing opportunity. The Vilcek family is super generous and has rewarded many immigrant scientists including Nobel Laureate @kkariko. Hope everyone eligible applies !
Scientek retweeted
Using the work flow of aptamer docking against the aptamers with known structures, none produced anything close to the actual structure. Fundamental problems include RNA (A) to DNA (B) form conversion, prediction without a target. So, be careful of docking chemrxiv.org/doi/full/10.264…
Scientek retweeted
Redox Reporter - Ligand Competition to Support Signaling in the Cocaine-Binding Electrochemical Aptamer-Based Biosensor (Dauphin-Ducharme, Johnson et al.) @ebiosensors and @philip_johnson8 onlinelibrary.wiley.com/doi/…
Scientek retweeted
High-Throughput Multiplexed Quantification of Molecules by Aptamer Sequencing (Apt-seq) in Single Cells | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/jac…
Scientek retweeted
Phototriggered LYTAC: Photoactive Bispecific Aptamer Chimera Enhances Targeted Degradation of Membrane Protein through Regulating Cell Autophagy | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/jac…
Scientek retweeted
A new mechanism for “RNA memory”! 😱
Thrilled to share another crazy paper from the lab (can’t believe we posted 2 in 2 days!), summarizing >10 years of research:
Work on transgenerational inheritance of small RNAs in the powerful model organism C. elegans changed how we think about what’s possible in inheritance and evolution, because it allows the most heretical thing: inheritance of parental responses to the environment! However, it’s still unclear whether RNAs are inherited across generations in other animals, largely because the RNA-dependent RNA polymerases that amplify heritable small RNAs and prevent their dilution in C. elegans are not conserved in mammals.
In this new work, an amazing collaboration with the Rink and Wurtzel labs, we show that planarians establish long-lasting and heritable small RNA–based gene regulatory states despite lacking canonical RNA-dependent RNA polymerases and nuclear RNAi machinery (that are required in C. elegans).
You might say “they are both worms…” BUT planarians are evolutionarily very distant from C. elegans (flatworms vs. roundworms, diverged more than 500 million years ago), making this particularly surprising. These are totally different animals.
We find that ingestion of double-stranded RNA induces sequence-specific silencing that persists for months and survives repeated cycles of whole-body regeneration. Even more strikingly, RNAi can be transferred between animals, echoing James V. McConnell’s controversial “RNA memory” experiments from the 1970s (his lab was targeted by the Unabomber terrorist Ted Kaczynski, who sent McConnell a bomb. This and other controversies ended this line of experiments…)
Mechanistically, we find that the response transitions from a transient systemic dsRNA-triggered phase to a stable, cell-autonomous post-transcriptional “memory phase” maintained by antisense small RNAs. Using a new luminescence reporter (transgenesis is currently impossible in planarians), we show that silencing spreads along the targeted gene and identify a weird type of planarian small RNAs with untemplated polyA tails.
RNAi inheritance without canonical RdRPs establishes planarians as a powerful system for studying RNA-based regulatory inheritance beyond C. elegans and raises the possibility that RNA-mediated inheritance may be more broadly conserved in animals, potentially even in mammals.
Here’s a video of a planarian that is treated by RNAi against β-catenin and develops multiple heads instead of just one. This is one of the phenotypes that is inherited. Another phenotype is “loss of eyes” (which we show is not only inherited across multiple regeneration cycles, but can also be transmitted between animals in transplantation experiments).
Amazing work led by first authors Prakash Cherian and Idit Aviram (co-supervised by Omri and me).
Please read the preprint, the link is in the next tweet, and share!



























