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Protein in embryo cells might be a reason for right- or left-handedness

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A young left handed child draws with a crayon on an easel.

Credit: incamerastock/Alamy

Left-handed people are almost three times more likely to have rare variants in the genes for tubulins, proteins that build cells’ internal skeletons. Tubulins assemble into long filaments called microtubules, which control the shapes and movements of cells. Microtubules could influence handedness because they form hair-like protrusions in cell membranes that can direct fluid flows in an asymmetric way during embryonic development.

Nature | 4 min read

Reference: Nature Communications paper

Super-Earth LHS 3844b is the first exoplanet to show convincing signs of tidal synchronization, meaning one of its hemispheres is permanently illuminated by its star and the other is in permanent darkness. The planet is relatively cool, indicating that it lacks the tidal heating non-locked planets experience. It’s unclear whether tidally locked planets could be habitable. These worlds “don’t have tides, or seasons or day–night cycles”, says astronomer and study co-author Nicolas Cowan. “Could you get the same kind of diversity and complexity of life evolving? I have no idea.”

Nature | 4 min read

Reference: The Astrophysical Journal paper

Biotechnology company LyGenesis has injected donor liver cells into a lymph node of a person with liver failure for the first time. The idea is that, within months, the donor cells will grow into a blood-filtering ‘miniature liver’. “It’s a very bold and incredibly innovative idea,” says liver-regeneration specialist Valerie Gouon-Evans. The treatment, which has been trialled in mice, dogs and pigs, might not relieve all of the complications of end-stage liver disease — but could provide a stopgap until a donor organ becomes available or make people healthy enough to undergo a transplant.

Nature | 5 min read

Nearly 20% of almost 600 image-containing papers that scientists compiled for a systematic review had suspicious images, including those that had been duplicated, stretched or rotated. Out of the 132 studies the researchers included in their final review, which was about a test to identify depression-related symptoms in rats, 10 contained potentially doctored images. Analysing these 10 alone assessed the test as 50% more effective than did the remaining 122 studies. This “clearly highlights [that falsified images] are impacting our consolidated knowledge base”, says systematic-review methodologist Alexandra Bannach-Brown.

Nature | 5 min read

Reference: bioRxiv preprint (not peer reviewed)

Features & opinion

When microbes’ ability to develop is pitted against their ability to make pharmaceuticals or biofuels, “the cells are going to choose to grow every time”, says synthetic biologist Brian Pfleger. To sidestep this unwinnable metabolic-resource war, researchers are introducing new biosynthesis pathways that can run alongside natural processes. For this, they have zeroed in on cofactors, small molecules that help enzymes do their work. Eventually, synthetic cofactors paired with the enzymes that use them could allow cells to churn out compounds more efficiently or even make those that rarely occur in nature.

Nature | 11 min read

With Twitter on the wane among many scientists — both as a place to post and a source of social-media data — some are turning to Reddit. Access to Reddit data is free for non-commercial researchers and academics. And its communities offer a space to network and chat, with an ‘upvote and downvote’ system helping good content rise to the top. Nature offers some context and advice for those looking to take the plunge.

Nature | 10 min read

Cancer cells make proteins found nowhere else in the body. Vaccines could teach the body’s immune system to recognise these proteins and destroy the cancer cells. The most powerful vaccines are created from the specific proteins extracted from a patient’s tumour and, in some cases, use the patient’s own immune cells. Researchers are also working on doing this vaccination process entirely within the body: first, drugs activate the immune system, then radiotherapy kills cancer cells, releasing the cancer proteins for the switched-on immune cells to find.

Nature | 4 min video

This article is part of Nature Outline: Cancer vaccines, an editorially independent supplement produced with the financial support from Moderna.

Where I work

Muh Aris Marfai measures the ground level compared to level zero of the sea (average sea level) using a geodetic digital level, at a tide gauge station at the Sunda Kelapa port of Jakarta, Indonesia.

Muh Aris Marfai is head of the Geospatial Information Agency of Indonesia in Bogor and a geography researcher at the Gadjah Mada University in Yogyakarta.Credit: Gaia Squarci for Nature

Geographer Muh Aris Marfai collects reference data for Indonesia’s coastal areas to prepare for the impacts of climate change. “Because so much of the country is surrounded by water, it’s important to pay attention to coastal areas,” he says. “Many coastal cities, including Jakarta, are experiencing subsidence owing to geological processes and coastal dynamics.” (Nature | 3 min read)

Quote of the day

Psychologist Jonathan Haidt’s blockbuster new book The Anxious Generation suggests that digital technologies are rewiring our children’s brains and causing an epidemic of mental illness — but its claims are not backed up by science, writes psychologist Candice Odgers. (Nature | 6 min read)

Today I’m enjoying the fish doorbell — a charming solution to alert the lock keepers of Utrech’s boat canal to let through migrating fish. A webcam allows watchers to ‘ring the doorbell’ for the fish, sending a photo to ecologists who signal that it’s time to clear the underwater traffic jam. The doorbell has struck a chord with nature-lovers, meaning the 950-ish slots for aspiring doorbell-ringers are often full. And even if you do get access, you might wait days to spot a fish in the murky waters. But all the enthusiasm is good news for ecologist Mark van Heukelum, who created the gadget. “We ‘only’ get a thousand pictures of every fish that appears for the camera,” he jokes on the fish-doorbell website.

Thanks for reading,

Flora Graham, senior editor, Nature Briefing

With contributions by Katrina Krämer

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Right- or left-handed? Protein in embryo cells might help decide

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A young left handed child draws with a crayon on an easel.

Dozens of genetic factors have been associated with left-handedness, which occurs in roughly one in ever ten people.Credit: incamerastock/Alamy

To what extent do genes determine how you pick up your morning cup of coffee? Researchers examined rare genetic variants from a database of more than 350,000 individuals’ genetic data to hunt for clues for what influences handedness in humans. Their findings implicate tubulins — proteins that build cells’ internal skeletons.

The results, published on 2 April in Nature Communications1, were obtained specifically at protein-coding parts of the DNA, and add to previous studies that linked genetic variations with handedness .

“This is an important and significant study” that supports tubulins’ involvement in determining the left–right brain asymmetry, says Sebastian Ocklenburg, a neuroscientist at the Medical School Hamburg in Germany.

During the embryonic stage of human development, the left and right brain hemispheres get wired differently, which in part determines innate behaviours, such as where we lean when we hug someone, on which side of our mouth we tend to chew our food and, most prominently, which hand is our dominant one. This turns out to be the left hand for around 10% of the human population.

Because most people have a clear preference for one hand over the other, finding genes linked to handedness can provide clues for the genetic basis of the brain’s left–right asymmetry.

Previous studies looking at genome-wide data from UK Biobank2 found 48 common genetic variants associated with left-handedness, which were mostly in non-coding regions of the DNA. These included sections that could control the expression of genes related to tubulins. These proteins assemble into long, tube-like filaments called microtubules, which control the shapes and movements of cells.

But Clyde Francks, a geneticist and neuroscientist at the Max Planck Institute for Psycholinguistics in Nijmegen, the Netherlands, and his team looked for genetic variants in protein-coding sequences. Their analysis of 313,271 right-handed and 38,043 left-handed individuals’ genetic data, from the UK Biobank, uncovered variants in a tubulin gene, dubbed TUBB4B, which were 2.7 times more common in left-handed people than in right-handers.

Microtubules could influence handedness because they form cilia — hair-like protrusions in cell membranes — which can direct fluid flows in an asymmetric way during development.

In spite of affecting only a small proportion of the people in this considerable data set, rare variants “can give clues to developmental mechanisms of brain asymmetry in everyone”, Francks says. He adds that these findings pave the way for future work to determine how microtubules, which themselves have a molecular ‘handedness’, can give an “asymmetric twist” to early brain development.

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Blueprinting extendable nanomaterials with standardized protein blocks

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Natural and previously designed proteins exhibit a wide range of helical geometries with local irregularities, kinks and deviations from linearity16 that make it difficult to achieve the properties illustrated in Fig. 1 that enable simple nanomaterial scaling (beyond the one dimension accessed by varying the number of repeats in a repeat protein or coiled coil). To achieve these properties, we designed a series of new building blocks constructed from ideal α-helices with all helical axes aligned. Restricting helical geometry to ideal straight helices with zero helical twist in principle considerably limits what types of structure could be built, but this is more than compensated by the great simplification of downstream material design, as illustrated below. We construct twistless helix repeat (THR) protein blocks from identical straight α-helices (typically 2–4 helices in each unit); the length of the blocks can be varied simply by varying the number of repeat units. In contrast to existing natural and designed repeat proteins17, THRs are constructed to enable modular nanomaterial design: linear blocks are perfectly straight, allowing nanomaterials to be extended and contracted with no alteration in the angles between the constituent monomers; curve blocks have smoothly curving trajectories that stay in-plane; and turn as well as interaction modules enable placement of two blocks in precise relative orientations with angles appropriate for regular material design.

We blueprint THRs by explicit placement of these straight helix structural elements using an extension of the principles used in coiled-coil and helical bundle design16,18. A first helix a0, part of the zeroth repeat, is placed at the origin and aligned to the z axis. A copy of a0 called a1 is then placed at a new location to set the rigid body transformation between the zeroth and first (and all subsequent) repeat units. After this, any other helices (b0, c0 …) that will be part of the repeating unit are placed as appropriate between a0 and a1 to provide more helices to pack against for stability, and the helices are connected with loops19; repetition of this basic unit then generates backbones with the desired geometries17 (Fig. 1b,c). As the helices are perfectly straight and parallel to the z axis, the overall repeat protein trajectory is fully defined by the following transformation parameters from a0 to a1: the distance of displacement in the xy plane from helical axis to helical axis (d), the change in displacement in the z axis direction (Δh) and the change in helix phase (Δθ; Fig. 1b). The remaining degrees of freedom for the positions of helices b0, c0 …, which define the internal geometry of the repeat, are extensively sampled, sequences are designed using Rosetta FastDesign or ProteinMPNN19,20, and designs are selected for experimental characterization on the basis of packing and sequence–structure consistency metrics (Methods). We obtained synthetic genes encoding the selected designs, expressed them in Escherichia coli and purified the proteins using nickel–nitrilotriacetic acid immobilized metal affinity chromatography. Designs that were solubly expressed were analysed by size-exclusion chromatography (SEC) to determine oligomerization state, and in the case of assemblies a subset was analysed by negative-stain electron microscopy (ns-EM). Experimental success rates and structural homogeneity for different classes of designs are summarized in Supplementary Figs. 1 and 2 and Supplementary Discussion.

To generate straight, linear THRs, we set Δθ to zero. As illustrated in Fig. 2a,b, this results in perfectly straight repeat proteins in which each repeat unit is translated but not rotated relative to the previous unit. There are two subclasses: setting Δh = 0 generates repeat proteins with each repeat unit simply displaced in the xy plane (Fig. 2a), whereas setting Δh to a non-zero value generates repeat proteins that also step along the z axis (Fig. 2b). We tested 33 linear THRs (with Δh = 0) with helices either about 20 or about 40 residues in height; 23 of 33 tested designs were solubly expressed, and 13 of 19 designs analysed by SEC were primarily monomeric as designed (Supplementary Figs. 1a,b and 2). Structural characterization of the linear building blocks by X-ray crystallography individually and/or cryogenic EM (cryo-EM) in the context of assemblies (see below) revealed that both the detailed internal structures and the overall straight linear geometry were successfully achieved. The backbone root mean square deviations (RMSDs) between the design models and crystal structures of three 20-residue helix designs (THR1, THR2 and THR3) and two 40-residue helix designs (THR5 and THR6) were 0.8, 0.8, 0.4, 0.6 and 1.3 Å, respectively, and in all five cases the relative rotation of successive repeats is nearly zero (Fig. 2a and Supplementary Fig. 6a). We found that we could not only control Δθ = 0, but also program values of the inter-repeat distance d: the crystal structure of a design with d set to a compact helix packing value of 8.7 Å had a very close value of 8.6–8.8 Å at its central interior (THR3), in contrast to most others designed at 10.0 Å (Supplementary Fig. 6b). For structural validation of blocks with non-zero Δh, the cryo-EM structure of an assembly constructed from such a block (THR4) exhibited a linear stair-stepping structure nearly identical to the design model, (backbone RMSD of 1.0 Å; Fig. 2b and Supplementary Fig. 1a).

Fig. 2: 1D and 2D shapes from THRs.
figure 2

a,b, The linear THR designs (rainbow) are nearly identical to the experimentally determined structures (grey). Side-chain sticks between α-carbon and β-carbon are shown to indicate helical phasing. a, Left: the 2.5-Å-resolution crystal structure of the short, linear THR1 has a 0.8 Å CA RMSD to the design. The inset below shows repeat packing in the THR interior. Right: the 2.7-Å-resolution crystal structure of the tall, linear THR5 has a 0.6 Å CA RMSD to the design. b, Bottom: Comparison of the stair-stepping linear THR4 design model to the cryo-EM structure (determined as part of a nanocage assembly; Supplementary Fig. 16). The CA RMSD between the cryo-EM structure and the design model is 1.0 Å. c, C4 and C3 polygons generated from four-helix turn module THRs as illustrated on the left. C4 square 90_C4_B (middle) and C3 triangle 120_C3_A (right) oligomers with representative ns-EM 2D class averages for comparison (raw EM micrographs are in Supplementary Fig. 1f). Chain breaks are at the ends of the rainbow sections. Scale bar, 4 nm (for the design models); class averages are not to scale. d, Uncapped curve THRs generate cyclic ring oligomers. The 12-repeat ring design (tested as C4) R12B has a cryo-EM 3D reconstruction overlaid on the model; the two are nearly identical. A 2D class average with the individual straight helices resolved is shown left of the ring. e, The 20-repeat ring design (tested as C4) R20A has an ns-EM reconstruction density overlaid on the model, and a raw micrograph is shown inside. Scale bar, 10 nm. f, The 30-repeat ring design (tested as C6) R30A represented in a similar manner to e. Scale bar in e, 10 nm (for the design models with reconstruction maps overlaid in df); class averages are not to scale. The asymmetric unit is coloured in rainbow.

To generate turn blocks, we blueprint an additional helix c0 lined up with a0 and a1 that can be assigned any specified phase difference, which can be utilized in fusion operations to produce a turn that is equal to θc − θa (Supplementary Fig. 5d,e). As for all of the THR blocks described here, because of the ideality of the block construction, the same sequence interactions can be used for the intra-block and inter-block interactions; we refer to blocks in which the terminal repeats have identical sequences to the internal repeats as uncapped, and those in which the terminal helices have polar outward-facing residues to prevent self-association (like the linear blocks above) as capped. We experimentally characterized uncapped turn modules that generate rotations of 360/n, in which n is 3, 4, 5 or 6; if the geometry is correct, these should oligomerize to form closed polygons with n subunits. ns-EM 2D class averages of the n = 3 designs clearly show the designed triangular shape with flattened corners (Fig. 2c and Supplementary Fig. 1f), and for n = 4, the designed square shapes (Fig. 2c and Supplementary Fig. 1f) including fine details such as the lower density around the corner helix are observed. For n = 5 and n = 6, success rates were lower, probably because their hinge regions involved less-extensive helix–helix interactions, but we did obtain designs with the expected polygonal structures for both after using reinforced corners on the C6 design (Supplementary Fig. 1f and Supplementary Discussion). Thus, by controlling the phase rotations between adjacent helices, turns can be encoded while maintaining overall parallel helical architecture. We also made polygonal designs with combinations of linear THRs and new straight helix-heterodimer corner junctions instead of turn modules (Supplementary Discussion and Supplementary Figs. 1g, 9 and 10).

To generate curve THRs, we incorporate a phase change (Δθ) between repeating elements (Fig. 1c) that generates a curved trajectory rather than a linear one. We choose Δθ to be a factor of 360° so that perfectly closed rings can be generated. The size of the closed ring can be controlled by specifying Δθ and the distance d between repeats (Supplementary Fig. 7). To access a broad range of d parameter values, we add additional helices to the repeat unit; for circular rings we used four helices per repeat unit. A full curve THR ring with n repeats can be divided into smaller chains each with m repeats, in which m is a factor of n; n/m uncapped repeats can associate to generate the full ring with cyclic symmetry21. To facilitate gene synthesis and protein production, we characterized such split oligomeric versions of the rings rather than synthesizing very long single chains. We designed rings with 12, 18, 20 and 30 repeats ranging from 9 to 22 nm in outside diameter. The 12- and 20-repeat rings were tested as C4 designs, whereas the 18- and 30-repeat rings were tested as C6 designs. Designs for all four ring sizes were remarkably uniform with ns-EM micrographs densely covered with circular assemblies with few to no defects or alternative structures present (Supplementary Fig. 7). Two-dimensional class averages showed that designs for all four sizes were close to the intended size (Fig. 2d; 10, 1 and 9 unique designs yielded distinct ring shapes for 18-, 20- and 30-repeat rings (Supplementary Figs. 1e and 2)). The smallest rings with 12 repeats have solvent-exposed helices exterior to the ring placed to facilitate outward-facing fusions without disrupting the core packing of the ring; these are clearly visible in the 2D class averages and 5.2-Å-resolution cryo-EM reconstruction of R12B (Fig. 2d and Supplementary Fig. 1e) that matches the designed patterning of the helices. ns-EM of the 18-, 20- and 30-repeat rings (with outside diameters of 12, 14 and 22 nm respectively) showed that many designs formed remarkably monodisperse populations of ring-like structures closely consistent with the design models (Fig. 2e,f and Supplementary Fig. 1e). ns-EM class averages of these designs had the smooth and round shape of the design models, and were in most but not all cases homogeneous (some designs assembled into closed-ring species that ranged by ±1 chain of the desired number, resulting in some slightly oblong shapes; Supplementary Fig. 1e). These designs highlight the control over ring curvature that can be achieved by specifying building block repeat rotation parameters.

The simplicity of our blocks in principle enables the reinforcing of designed materials using struts rigidly linking distinct structural elements. As a first test of this, we sought to build concentric ring assemblies from pairs of rings that have different sizes but repeat numbers that share large common denominators. For example, 2 repeat units of a 20-repeat ring can be combined with 3 repeat units of a 30-repeat ring as 10 copies generate a complete ring in both cases (Fig. 3a, left). Rings were segmented into matching cyclic symmetries, the rotation and z displacement of one ring relative to the other was sampled, and linear THRs were placed to connect the inner and outer rings. We constructed single-component C10 concentric ring assemblies by connecting a three-repeat-unit curved block and a two-repeat-unit curved block that both generate a 36° (360°/10) rotation with a radially oriented strut. Two-dimensional class averages of ns-EM images of the designed strutted assemblies show both rings clearly present (Fig. 3a, right; some 11-subunit rings were observed in addition to the target 10-subunit structure). We similarly connected three repeat units with a 20° rotation per repeat, and five repeat units with a 12° rotation per repeat, with a radial strut; the resulting composite subunits map out a 60° rotation of inner and outer rings such that six subunits generate a full 360° ring. The resulting two-component C6 strutted assembly yielded 2D class averages that showed both rings with all chains present, and a 5.1-Å cryo-EM reconstruction was very close to the design model (RMSD 2.7 Å) with very similar outer diameter (19.7 nm versus 20.1 nm; Fig. 3b and Supplementary Fig. 8c). The helix positioning in the inner ring and the strut are also very close to the design model (Supplementary Fig. 8c, insets). Thus, the modularity of the THRs enables designing complex structures by inspection, and enables buttressing to increase structural robustness (Supplementary Discussion and Supplementary Fig. 8).

Fig. 3: Design of strutted double rings.
figure 3

a,b, Two different size rings built from curve THRs for which integral multiples generate the same rotation can be concentrically nested and connected by struts. a, Three repeats of an outer ring (12° per repeat) are combined with two repeats of an inner ring (18° per repeat) that both generate a 36° rotation. Connection of the two pieces with a linear THR generates a C10 single-component ring (strut_C10_8); an asymmetric unit is highlighted in the second ring image. An ns-EM 3D reconstruction in C10 symmetry is shown overlaid with the design model next to 2D class averages and a representative micrograph. b, Five repeats of an outer ring (12° per repeat) are combined with three repeats of an inner ring (20° per repeat) that both generate a 60° rotation. Connection of the two pieces with a linear THR and an additional chain break in the outer ring generates a C6 two-component ring (strut_C6_21); an asymmetric unit is highlighted in the second ring image with the two chains in different colors. A cryo-EM 3D reconstruction in C6 symmetry is shown overlaid with the design model next to cryo-EM 2D class averages and a representative ns-EM micrograph (additional cryo-EM details are provided in Supplementary Fig. 8c). Scale bars, 20 nm (a,b). An asymmetric unit is outlined on top of the design model, and repeats are sectioned with dashed lines.

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