Image of aggregated anthrobots (green) forming a bridge between two neuronal cells (red).
Anthrobots aggregated together to form a superbot bridge (green) which facilitated healing between neuronal cells (red).

Building Living Bridges with Anthrobots

Researchers used adult human cells to craft biological robots capable of movement and more.

Image Credit:

Gizem Gumuskaya

Image of Gizem Gumuskaya working under a laboratory fume hood.
Gizem Gumuskaya blended her architectural background with synthetic biology to develop living, self-constructing, biological structures.
Gizem Gumuskaya

Growing up in Turkey, synthetic biologist Gizem Gumuskaya was enamored with architecture and how buildings emerged from the bustling chaos of the city. She found that designed environments mirrored biology, as nature, the ultimate architect, constructs complex structures from a single cell.

This led her to seek graduate research that harnessed biology as a working medium in Michael Levin’s lab at Tufts University. Intrigued by Levin and his colleagues’ previous work, which combined artificial intelligence designs and embryonic frog cells to create living biological robots that could swim and self-replicate, Gumuskaya was eager to test whether this would function in a non-froggy model.“I wanted to build something that evolution didn’t already design for us,” she said.

She combined her engineering mindset and the self-organization of biology to create mammalian-derived living robots, anthrobots, from adult human tracheal cells.2 The adult cells displayed morphologic plasticity and self-assembled into ciliated spheres that enabled them to wiggle and swim through their environments. Not only could they move, but anthrobots spontaneously fused to form larger structures called superbots.

When Gumuskaya explored the anthrobots’ influence on other cells, the results surprised her. When they studied images of these cultures, they saw that these superbots formed a bridge-like structure that connected to a layer of damaged human neurons. This structure resembled an ant bridge, a concept from Gumuskaya’s architecture studies. Like how ant colonies function as a superorganism, the superbots showed enhanced capabilities of teamwork, collectively aiding in the healing of damaged neurons. However, the exact mechanism remains unclear, Gumuskaya noted.

Anthrobots, an extension of their amphibious predecessor, hold promise for biological applications. “Anthrobots are just one example of what we can accomplish by thinking about nature as a design medium. I hope the scientific community will look at cells through this lens and imagine how to create other machines,” remarked Gumuskaya.

Correction: August 19, 2024. The story has been updated to accurately reflect Gumuskaya's affiliations and projects.

Conceptual illustration of researchers studying microbes in a petri dish.

Next-Level Screening for Antimicrobial Resistance

Bacterial isolate screening improves surveillance, stewardship, and infection control.

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© istock.com, sorbetto

Antimicrobial resistance (AMR) is a serious and growing problem for which the current arsenal of antibiotics is insufficient and the availability of new treatments is limited.1 As a result, identifying and monitoring the pervasiveness of resistant microbes is critical to early mitigation approaches. Researchers seek effective strategies to test for the AMR genes that underlie a broad range of resistance mechanisms, including extended-spectrum β-lactamases, carbapenemases, and plasmid-mediated ampC.2 This can often be challenging, given the need for rapid techniques that are broad enough to capture the many gene variants, yet sensitive and specific enough to generate robust and reliable data.

          Conceptual image of a scientist pipetting liquid from a vial, showing a blue gloved hand on the right and a pipette tip on the left.
Streck ARM-D Kits are an ideal method to screen bacterial isolates for antimicrobial resistance after phenotypic testing and before whole genome sequencing. For research use only. Not for use in diagnostic procedures.
STRECK

Real-time reverse transcription polymerase chain reaction (RT-PCR) assays are routinely used to identify small quantities of target molecules. While this approach is the gold standard for many applications, traditional methodologies do not provide scientists with the speed and multiplexing capabilities that are required to meet the detection needs of large-scale pathogen screening.

As a result, scientists pursuing AMR research seek novel tools to streamline molecular testing workflows and output. For example, Streck ARM-D kits enable AMR screening after phenotypic testing and before whole genome sequencing. These ready to use kits contain the full suite of reagents and controls, with straightforward protocols and data analysis. The comprehensive ARM-D RT-PCR kits are fast, reliable, sensitive, and specific, and detect over one thousand variants from over two dozen AMR gene target families for superior antibiotic resistance surveillance, infection control, and antibiotic stewardship efforts.

Learn more about AMR molecular testing.

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Sperm Speed Up with Ultrasound

A team demonstrated that ultrasound waves improved motility in sperm.

Low sperm motility reduces fertilization success and embryo quality in traditional and assisted conception. A research team used ultrasound waves as a form of mechanotherapy, which alters cell metabolic activity, to increase immotile sperm’s physical activity.1 They investigated this approach at a single cell level using microfluidics.2  

     An infographic showing how ultrasound waves improved motility in sperm.
Illustrated by Ashleigh Campsall


  1. Devendran C, et al. Adv Sci. 2019;6(24):1902326
  2. Vafaie A, et al. Sci Adv. 2024;10(7):adk2864
A 3D rendering of an antibody drug conjugate with attached cytotoxic payloads.

Supporting Antibody-Drug Conjugate Development

Industry expertise helps scientists navigate and streamline antibody-drug conjugate research and development.

Image Credit:

© istock.com, Marcin Klapczynski

A lack of targeting specificity has been a long-running problem for cytotoxic anticancer agents, with excess side effects limiting their effectiveness. Scientists have turned to antibodies, and their natural targeting affinity, as a potential solution. Antibody-drug conjugates (ADC) combine the tumor-targeting potential of antibodies with the potency of cytotoxic drugs, and have been called a “magic bullet” for cancer therapeutics.1 

          A rendering of a single antibody drug conjugate molecule, featuring a central antibody and four drug molecules conjugated to the heavy chain. 
Antibody-drug conjugates combine the tumor-targeting potential of antibodies with the potency of cytotoxic drugs.
sino biological; © istock.com, mesh cube

ADC are comprised of three principle units: the antibody, the linker, and the payload.1 When designing or selecting an antibody, researchers must consider not only antigen binding specificity, but also serum half-life and internalization rates. The latter two factors affect an ADC’s ability to reach its target and deliver its payload inside the cell. The linker, as well as how it is conjugated to the antibody, mediates ADC stability and facilitates payload release. Finally, the payload must possess low immunogenicity and high stability under physiological conditions in addition to high potency. It also needs to be cell membrane permeable in order to enter target cells. 

ADC are complex agents that require considerable care and resources during development. As such, scientists working with ADC face considerable challenges as they move through design, preclinical and clinical testing, and manufacturing. Here, as with drug development in general, industry support can prove essential to moving an agent from the bench to the bedside. Companies such as Sino Biological are deeply engaged in every aspect of ADC development, from antibody discovery and optimization to animal model evaluation and clinical trials. 

Read more about how Sino Biological offers reagents, kits, and testing solutions tailored to researchers’ specific needs.

What type of support is helpful when developing antibody-based therapies?

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Two scientists at a table with two petri dishes of mold. One scientist opens a cloche revealing a meat-like patty made of koji mold.

Mold Burger: Coming Right Up

From the laboratory to the table, researchers cooked bioengineered fungi into a tempting patty.

Image Credit:

Modified from © istock.com, zuperia; Designed by Ashleigh Campsall

A person holding up two petri dishes side by side.
Hill-Maini holds up two petri dishes with the original mold (left) and the CRISPR-Cas9 edited mold (right).
Marilyn Sargent, Berkeley Lab

Fungi are the versatile thread connecting bread, cheese, alcohol, and soy sauce, infusing each with distinct flavors. While fungi are deeply interconnected with food production, Vayu Hill-Maini, a chef turned bioengineer at the University of California, Berkeley, was inspired to innovate fungal alternatives to improve food sustainability.

Recently, Hill-Maini and his team modified genes in Aspergillus oryzae (A. oryzae) to create a visually appealing meat-like patty. Their creation, reported in Nature Communications, showcased the possibilities of bringing gene-edited fungi to the table.1

“We thought about the potential of fungi and how it can be unlocked by tinkering with what was already there [in the genome],” said Hill-Maini.

Hill-Maini used A. oryzae, commonly known as koji mold, for his experiment. Using clustered regulatory interspaced palindromic repeats (CRISPR), the team overexpressed two genes: one that produced ergothioneine, an antioxidant found in fungi, and one that coded for heme, a molecule that gives meat its color and distinct flavor.

A koji mold patty after frying looks much like its meat counterpart.
Hill-Maini harnesses the potential of the existing genome in fungi to create appealing new fungal foods.
Vayu Hill-Maini

Three days later, the once white fungi grew red and were ready to harvest. After removing excess water and grinding the fungi into a patty, the researchers threw it on the grill. The result was a sizzling meat-like patty with a tantalizing smell. Their proof-of-concept experiment demonstrated ways to boost nutritional value and sensory appeal of the fungal patty in food preparation. 

“It’s a novel idea using whole filamentous fungi cells as the main food ingredient instead of isolating a fungal product,” said Yong-Su Jin, a food microbiologist and bioengineer at the University of Illinois at Urbana-Champaign, who was not involved in the study. However, Jin lamented the lack of a taste test of the creation.

Next, the researchers want to explore the genes that control the mold’s texture. “This work can inspire us to think about what food can be and what is possible,” said Hill-Maini. “It is just the starting point to pushing the boundaries in food sustainability.” 

  1. Maini Rekdal V, et al. Nat Commun 2024;15:2099.
A river surrounded by trees with mountains in the background.

DNA Metabarcoding Reveals Hidden Biodiversity

Genomicist Mehrdad Hajibabaei empowers Canadian communities to monitor bioindicator species in their local freshwater ecosystems.

Image Credit:

© istock.com, Schroptschop

A headshot Mehrdad Hajibabaei smiling in front of a shoreline.
Mehrdad Hajibabaei combines citizen science and DNA metabarcoding to improve scientific understanding of freshwater ecosystems.
Mehrdad Hajibabaei

Healthy freshwater ecosystems are crucial for supporting wildlife and supplying humans with necessities like food, water, energy, and transportation. Despite this, there is a remarkable lack of data on the status of many waterways, especially in large, sparsely populated countries like Canada.

The citizen science project Sequencing The Rivers for Environmental Assessment and Monitoring (STREAM), led by Mehrdad Hajibabaei at the University of Guelph, aims to close these data gaps through partnerships with communities across the country. In STREAM, community members collect samples of river sediment and send them to the Hajibabaei laboratory, where researchers analyze the diversity of bottom-dwelling invertebrates and certain types of microalgae as bioindicators of ecosystem health.1

Historically, this would have required extensive evaluation by highly trained taxonomists painstakingly sorting one miniscule species from another under the microscope. To streamline this process, Hajibabaei and his team use DNA metabarcoding. After extracting DNA from the substrate samples, they amplify and sequence specific sections of the genome that are highly variable between species. Then, using the bioinformatics pipeline MetaWorks, they compare these identifying “barcodes” to a DNA reference library to determine which species are present.

Researchers can use these data for large-scale projects, like investigating the role of biodiversity in ecosystem function or the effect of climate change on freshwater species. They also use the data to answer questions about local ecosystem health posed by the community, such as whether a problematic invasive species is present, or whether restoration efforts are having the desired effects.

“We are basically democratizing access to biodiversity data,” said Hajibabaei. “Biodiversity is vast, but a lot of it is too small for us to see. The technologies that we have now will allow us to see that biodiversity through the lens of DNA, and let anyone, anywhere, access that information… hopefully leading towards a society that values biodiversity more.”

Want to submit your own citizen science project? 

Tell Us About It

  1. Robinson CV et al. Ecol Indic. 2022;145:109603.
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Two cells on a purple background. Two mechanisms of gene silencing are shown in the cell on the left, while a double-strand break in a DNA region is shown in the cell on the right.

What’s the Difference Between Gene Knockdown and Gene Knockout?

There are many techniques that allow scientists to silence a gene, but whether the effect is transient or permanent depends on the type of approach.

Image Credit:

Illustrated by Imran Chowdhury

Researchers can experimentally interrogate the function of one or more genes using knockout or knockdown tools. Although both approaches ultimately interfere with gene function, knockout and knockdown techniques accomplish this through distinct mechanisms that operate at different levels.

Gene Knockdown: A Short-term Trick

Gene knockdown reduces the expression of a gene at the RNA level. Scientists often employ RNA interference (RNAi) and clustered regularly interspaced short palindromic repeats interference (CRISPRi) methods to accomplish that goal. While RNAi exploits the naturally occurring RNAi pathway used by cells to identify and target a specific messenger RNA for degradation, CRISPRi binds to the DNA and blocks either transcription initiation or elongation depending on the region it binds to.1,2 Since both techniques act at the transcript level, there are no changes in the DNA sequence of the gene, leading to a transient phenotypic effect. Researchers opt for this temporary gene silencing when studying genes that are essential for the development of an organism and whose deletion could be lethal. 

Gene Knockout: Altering the Genetic Blueprint

Gene knockout approaches completely ablate gene expression at the DNA level.3 Researchers can accomplish this by using genome editing tools, such as zinc finger nucleases (ZFN), transcription activator-like effector nucleases (TALEN), and CRISPR and its associated endonucleases.4-6 These tools produce double-strand breaks at specific DNA sites, which the cell tries to fix using an error prone repair mechanism that can alter the sequence of the target gene. As knockout tools result in a sustained gene silencing, they eliminate confounding effects that might remain after gene knockdown.

August 2024 crossword puzzle

Science Crossword Puzzle

Put on your thinking cap, and take on this fun challenge.

Image Credit:

Modified from © istock.com, zuperia; Designed by Ashleigh Campsall

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