Translational symmetry in convolutions with localized kernels causes an implicit bias toward high frequency adversarial examples.

Adversarial attacks are still a significant challenge for neural networks. Recent efforts have shown that adversarial perturbations typically contain high-frequency features, but the root cause of this phenomenon remains unknown. Inspired by theoretical work on linear convolutional models, we hypothesize that translational symmetry in convolutional operations together with localized kernels implicitly bias the learning of high-frequency features, and that this is one of the main causes of high frequency adversarial examples. To test this hypothesis, we analyzed the impact of different choices of linear and non-linear architectures on the implicit bias of the learned features and adversarial perturbations, in spatial and frequency domains. We find that, independently of the training dataset, convolutional operations have higher frequency adversarial attacks compared to other architectural parameterizations, and that this phenomenon is exacerbated with stronger locality of the kernel (kernel size) end depth of the model. The explanation for the kernel size dependence involves the Fourier Uncertainty Principle: a spatially-limited filter (local kernel in the space domain) cannot also be frequency-limited (local in the frequency domain). Using larger convolution kernel sizes or avoiding convolutions (e.g., by using Vision Transformers or MLP-style architectures) significantly reduces this high-frequency bias. Looking forward, our work strongly suggests that understanding and controlling the implicit bias of architectures will be essential for achieving adversarial robustness.

Towards molecular controlled magnonics.

Magnonics is an emerging field broadly recognized as a paradigm shift for information technologies based on the use of spin waves. However, the low flexibility and variety of the existing systems still hamper their applications. Herein, we propose an unprecedented chemical approach to magnonics based on the creation of hybrid molecular/2D heterostructures. We analyse the modulation of the magnetic properties, magnon dispersion and spin dynamics of a single layer of CrSBr after the deposition of sublimable organic molecules via first-principles calculations. Our results predict a modulation of magnetic exchange, a shift in the magnon frequencies and an enhancement of their group velocities up to ∼7%. Interestingly, we find a linear correlation between these effects and the donor character of the molecules. This will pave the way for the design of a new class of magnonic materials that can be selectively tailored by a chemical approach.

Unravelling the role of spin-vibrational coupling in designing high-performance pentagonal bipyramidal Dy(iii) single ion magnets.

At the cutting edge of high-performance single-molecule magnets (SMMs) lie lanthanide-based complexes, renowned for their potent magnetic anisotropy. SMMs containing one metal centre are defined as single-ion magnets (SIMs). The performance of SMMs is measured generally via the barrier height for magnetisation reversal (Ueff) and blocking temperature (TB), below which the magnetisation is fully frozen. To enhance the Ueff and TB values in lanthanide-based SMMs, the static crystal field splitting of mJ levels has been effectively adjusted through ligand design, leveraging the oblate/prolate ground state 4f electron density shape. However, the maximum fine-tuning achievable through ligand design, known as the axial limit, has already been reached in this class of compounds. This necessitates new design principles to enhance SMM characteristics to better suit end-user applications. Among other avenues that can be explored to improve SMM characteristics, a deeper understanding of spin-phonon coupling is critical to advancing TB values. However, there are only a handful of examples where this has been deciphered. In this work, using a combination of DFT and ab initio CASSCF calculations, we have performed spin-phonon calculations on five classes of pentagonal bipyramidal Dy(iii) SIMs exhibiting TB values in the range of 4.5 K to 36 K ([Dy(bbpen)Br] (1, H2bbpen = N,N'-bis(2-hydroxybenzyl)-N,N'-bis(2-methylpyridyl)ethylenediamine), [Dy(OCMe3)Br(THF)5][BPh4] (2) [Dy(OSiMe3)Br(THF)5] [BPh4] (3), [Dy(LN5)(Ph3SiO)2](BPh4)·CH2Cl2 (4) and [L2Dy(H2O)5][I]3·L2·H2O (5, L = tBuPO(NHiPr)2)). Unlike the method employed elsewhere for the calculation of spin-phonon coupling, in this work, we have employed a set of criteria and intuitively selected vibrational modes to perform the spin-phonon coupling analysis. The approach provided here not only reduces the computational cost significantly but also suggests chemical intuition to improve the performance of this class of compounds. Our calculations reveal that low-energy vibrational modes govern the magnetisation relaxation in these SIMs. A flexible first coordination sphere found on some of the complexes was found to be responsible for low-energy vibrations that flip the magnetisation, reducing the TB values drastically (complexes 2 and 3). On the other hand, a rigid first coordination sphere and a stiff ligand framework move the spin-vibrational coupling that causes the relaxation to lie beyond the secondary coordination sphere, resulting in an increase in TB values. Our calculations also reveal that not only the atoms in the first coordination sphere but also those in the secondary coordination sphere affect the performance of the SMMs. Learning from this exercise, we have undertaken several in silico models based on these vibrations to improve the TB values. Some of these predictions were correlated with literature precedents, offering confidence in the methodology employed. To this end, our comprehensive investigation, involving twenty-three molecules/models and five sets of geometries for pentagonal bipyramidal Dy(iii) single-ion magnets (SIMs), unveils a treasure trove of chemically sound design clues, poised to enhance the TB values in this fascinating molecular realm.

Magnetic anisotropy in octahedral Dy(III) and Yb(III) complexes.

New organophosphate complexes [Ln(dippH)3(dippH2)3]·(H2O)6, (Ln = Dy, Yb and Y; dippH2 = 2,6-diisopropylphenyl phosphate), displaying octahedral coordination geometry around the metal ion, exhibit unusual slow relaxation of magnetisation, which is investigated through experimental studies and ab initio CASSCF calculations.

Core-ionization spectrum of liquid water.

We present state-of-the-art calculations of the core-ionization spectrum of water. Despite significant progress in procedures developed to mitigate various experimental complications and uncertainties, the experimental determination of ionization energies of solvated species involves several non-trivial steps such as assessing the effect of the surface potential, electrolytes, and finite escape depths of photoelectrons. This provides a motivation to obtain robust theoretical values of the intrinsic bulk ionization energy and the corresponding solvent-induced shift. Here we develop theoretical protocols based on coupled-cluster theory and electrostatic embedding. Our value of the intrinsic solvent-induced shift of the 1sO ionization energy of water is -1.79 eV. The computed absolute position and the width of the 1sO peak in photoelectron spectrum of water are 538.47 eV and 1.44 eV, respectively, agreeing well with the best experimental values.

Total Synthesis, Revised Structure, and Biological Evaluation of Elgonene B and Analogues.

Herein, we report the first total synthesis of elgonene B and its congeners, thus resulting in a revision of the configuration at the C-6 carbon of the originally proposed structure of elgonene B. This synthetic approach demonstrates the utility of several important reactions such as the chiral oxazaborolidinium ion-catalyzed Diels-Alder reaction, Ando's Horner-Wadsworth-Emmons olefination, and the intermolecular Nozaki-Hiyama-Kishi reaction as key steps. Additionally, the study explores the cytotoxic and antibacterial activities of elgonene B and its congeners (1-4).

Phytoconstituents from Urtica dioica (stinging nettle) of Sikkim Himalaya and their molecular docking interactions revealed their nutraceutical potential as α-amylase and α-glucosidase inhibitors.

In this study, antioxidative methanolic leaf extract (MeOH-SIS) of Urtica dioica was characterized for anti-diabetic activity. The extract was purified on a column to yield seven homogenous fractions (F1-F7) which were further determined for DPPH radical scavenging activity. MeOH-SIS and the fraction F1 (selected based on % yield and activity) were evaluated for their in vitro α-amylase and α-glucosidase inhibitory activity. The results showed inhibition of both enzymes in a dose dependent manner and F1 exhibited relatively higher inhibition than its mother extract MeOH-SIS. GC-MS analyses of both the extracts identified 24 major compounds among which 10 were previously described as bioactive compounds. Among all, 5 compounds demonstrated to have quality pharmacokinetics profiles and were examined for possible binding affinity against the active sites of α-amylase and α-glucosidase using molecular docking. The binding interaction of 2R-acetoxymethyl-1,3,3-trimethyl-4 T-(3-methyl-2-buten-1-yl)-1 T-cyclohexanol within the active sites of the target receptors was found to be significant among others, and can be developed as a potential inhibitor of α-amylase and α-glucosidase. The leaf extract can be utilized to develop food additive for the control and management of oxidative stress induced diabetes.

Field-induced SIM behaviour in early lanthanide(III) organophosphates containing 18-crown-6.

Single-ion magnets (SIMs) have attracted wide attention in recent years. Despite tremendous progress in late lanthanide SIMs, reports on early lanthanides exhibiting SIM characteristics are scarce. A series of five novel 18-crown-6 encapsulated mononuclear early lanthanide(III) organophosphates, [{(18-crown-6)Ln(dippH)3}{(18-crown-6)Ln(dippH)2(dippH2)}]·[I3] [Ln = Ce (1), Pr (2), Nd (3)] and [{Ln(18-crown-6)(dippH)2(H2O)}·{I3}] [Ln = Sm (4) and Eu (5)], have been synthesised in the present study. 18-crown-6 coordinates to Ln(III) ions in an equatorial position while the axial positions are occupied by either three phosphate moieties as in 1-3 or two phosphate moieties and one water molecule as in 4 and 5, resulting in a muffin-shaped coordination geometry around the Ln(III) centres. Magnetic susceptibility measurements reveal that Ce and Nd complexes are field-induced single-ion magnets with significant barrier heights. Furthermore, the ab initio CASSCF/RASSI-SO/SINGLE_ANISO calculations on complexes 1 and 3 reveal significant QTM in the ground state rationalising the field-induced single-ion magnetism behaviour of these complexes.

Pushing the Boundary of Covalency in Lanthanoid-Tellurium Bonds: Insights from the Synthesis, Molecular and Electronic Structures of Low-Coordinate, Monomeric Europium(II) and Ytterbium(II) Tellurolates.

Owing to the strict hard/soft dichotomy between the lanthanoids and tellurium atoms, and the strong affinity of lanthanoid ions for high coordination numbers, low-coordinate, monomeric lanthanoid tellurolate complexes have remained elusive as compared to the lanthanoid complexes with lighter group 16 elements (O, S, and Se). This makes the development of suitable ligand systems for low-coordinate, monomeric lanthanoid tellurolate complexes an appealing endeavor. In a first report, a series of low-coordinate, monomeric lanthanoid (Yb, Eu) tellurolate complexes were synthesized by utilizing hybrid organotellurolate ligands containing N-donor pendant arms. The reaction of bis[2-((dimethylamino)methyl)phenyl] ditelluride, 1 and 8,8'diquinolinyl ditelluride, 2 with Ln0 metals (Ln=Eu, Yb) resulted in the formation of monomeric complexes [LnII (TeR)2 (Solv)2 ] [R=C6 H4 -2-CH2 NMe2 ] [3: Ln=Eu, Solv=tetrahydrofuran; 4: Ln=Eu, Solv=acetonitrile; 5: Ln=Yb, Solv=tetrahydrofuran; 6: Ln=Yb, Solv=pyridine] and [EuII (TeNC9 H6 )2 (Solv)n ] (7: Solv=tetrahydrofuran, n=3; 8: Solv=1,2-dimethoxyethane, n=2), respectively. Complexes 3-4 and 7-8 represent the first sets of examples of monomeric europium tellurolate complexes. The molecular structures of complexes 3-8 are validated by single-crystal X-ray diffraction studies. The electronic structures of these complexes were investigated using Density Functional Theory (DFT) calculations, which revealed appreciable covalency between the tellurolate ligands and lanthanoids.

Long Non-coding RNAs, Lnc(ing) RNA Metabolism to Cancer Biology.

The eukaryotic genome is represented by a vast proportion of non-coding regions, which in recent years have been attributed to have important functional roles in gene regulation through a myriad of processes, ranging from proper localization, correct folding and, most importantly, spatial and temporally regulated expression of genes. One of the major contributing factors in these processes is ribonucleic acid (RNA) metabolism, which comprises the RNA-nucleoprotein (RNP) complexes that interact with and instruct the genome to function. Long non-coding RNAs are an integral component of several RNPs, and herein we provide an overview of the understanding of the long non-coding RNAs, their characteristics, their function and their balancing act as dual modulators in cancer manifestation and progression.

Experimental and theoretical investigations on three DyIII4 single molecule magnets: structural and magneto-structural correlations.

The work in this report describes the syntheses, crystal structures, dc/ac magnetic behaviour, and theoretical calculations (both ab initio CASSCF and DFT) of three defect dicubane/planar butterfly type tetradysprosium(III) compounds of compositions [DyIII4L4(µ3-OH)2(carboxylate)2(dmf)2] (carboxylate = formate (1), acetate (2), propionate (3)), where H2L = 2-(2-hydroxy-3-ethoxybenzylideneamino)phenol. In the butterfly type structures, two DyIII centres (Dyb) occupy the body positions while two other (Dyw) units occupy the wing positions. SHAPE analyses reveal that the coordination geometries of the Dyb and Dyw centres, both octacoordinated, are triangular dodecahedron (TDD) and square antiprism (SAPR), respectively. Variable-temperature magnetic susceptibility measurements give an indication of weak antiferromagnetic interactions and variable-field magnetization measurements reveal strong anisotropy in all the three compounds. The variable-temperature/frequency in-phase/out-of-phase AC susceptibility data reveal that all these three compounds are SMMs with two relaxation channels under zero dc field; slow relaxation (SR) and fast relaxation (FR) processes could be assigned to the SAPR (Dyw) and TDD (Dyb) metal centres, respectively. The simulated Ueff and τ0 values are: 49.0 cm-1 and 1.76 × 10-7 s for 1, 30.3 cm-1 and 1.51 × 10-8 s for 2 and 23.4 cm-1 and 9.64 × 10-7 s for 3. Furthermore, ab initio CASSCF/RASSI-SO/SINGLE_ANISO calculations reveal that the ground state of DyIII centres are axial in nature with a dominating contribution from mJ = |±15/2>. The magnetization relaxation occurs via the first excited KD resulting in the large computed blocking barrier of Dyw (SAPR) centres compared to that of the Dyb (TDD) centres which corroborates the experimental measurements. The exchange parameters obtained from DFT calculations are generally in line with those obtained from the fitting of χMT vs. T in POLY_ANISO calculations. Interesting structural and magneto-structural correlations have been found, which are the major outcomes of this investigation.

Analysis of the Magnetic Coupling in a Mn(II)-U(V)-Mn(II) Single Molecule Magnet.

[{Mn(TPA)I}{UO2(Mesaldien)}{Mn(TPA)I}]I formula (here TPA=tris(2-pyridylmethyl)amine and Mesaldien=N,N'-(2-aminomethyl)diethylenebis(salicylidene imine)) reported by Mazzanti and coworkers (Chatelain et al. Angew. Chem. Int. Ed. 2014, 53, 13434) is so far the best Single Molecule Magnet (SMM) in the {3d-5f} class of molecules exhibiting barrier height of magnetization reversal as high as 81.0 K. In this work, we have employed a combination of ab initio CAS and DFT methods to fully characterize this compound and to extract the relevant spin Hamiltonian parameters. We show that the signs of the magnetic coupling and of the g-factors of the monomers are interconnected. The central magnetic unit [UV O2 ]+ is described by a Kramers Doublet (KD) with negative g-factors, due to a large orbital contribution. The magnetic coupling for the {Mn(II)-U(V)} pair is modeled by an anisotropic exchange Hamiltonian: all components are ferromagnetic in terms of spin moments, the parallel component JZ twice larger as the perpendicular one J⊥ . The spin density distribution suggests that spin polarization on the U(V) center favors the ferromagnetic coupling. Further, the JZ /J⊥ ratio, which is related to the barrier height, was found to correlate to the corresponding spin contribution of the g-factors of the U(V) center. This correlation established for the first time offers a direct way to estimate this important ratio from the corresponding gS -values, which can be obtained using traditional ab initio packages and hence has a wider application to other {3d-5f} magnets. It is finally shown that the magnetization barrier height is tuned by the splitting of the [UV O2 ]+ 5 f orbitals.

Whole genome sequencing and comparative genomic analyses of Pseudomonas aeruginosa strain isolated from arable soil reveal novel insights into heavy metal resistance and codon biology.

Elevated concentration of non-essential persistent heavy metals and metalloids in the soil is detrimental to essential soil microbes and plants, resulting in diminished diversity and biomass. Thus, isolation, screening, and whole genomic analysis of potent strains of bacteria from arable lands with inherent capabilities of heavy metal resistance and plant growth promotion hold the key for bio remedial applications. This study is an attempt to do the same. In this study, a potent strain of Pseudomonas aeruginosa was isolated from paddy fields, followed by metabolic profiling using FTIR, metal uptake analysis employing ICP-MS, whole genome sequencing and comparative codon usage analysis. ICP-MS study provided insights into a high degree of Cd uptake during the exponential phase of growth under cumulative metal stress to Cd, Zn and Co, which was further corroborated by the detection of cadA gene along with czcCBA operon in the genome upon performing whole-genome sequencing. This potent strain of Pseudomonas aeruginosa also harboured genes, such as copA, chrA, znuA, mgtE, corA, and others conferring resistance against different heavy metals, such as Cd, Zn, Co, Cu, Cr, etc. A comparative codon usage bias analysis at the genomic and genic level, whereby several heavy metal resistant genes were considered in the backdrop of two housekeeping genes among 40 Pseudomonas spp. indicated the presence of a relatively strong codon usage bias in the studied strain. With this work, an effort was made to explore heavy metal-resistant bacteria (isolated from arable soil) and whole genome sequence analysis to get insight into metal resistance for future bio remedial applications.

In silico design criteria for high blocking barrier uranium (III) SIMs.

A combination of DFT and ab initio CASSCF/PT2 calculations on U(III) fictitious models and numerous reported X-ray structures unveils several geometries from coordination number 1 to 12 that can be targeted to design potential U(III) SIMs with attractive barrier heights. Among the geometries studied, the T-shaped and capped pentagonal antiprism geometries yield values exceeding 1500 cm-1 - a value that is elusive for any uranium SIMs.

Detection of SARS-CoV-2 RNA Using a DNA Aptamer Mimic of Green Fluorescent Protein.

RNA detection is important in diverse diagnostic and analytical applications. RNAs can be rapidly detected using molecular beacons, which fluoresce upon hybridizing to a target RNA but require oligonucleotides with complex fluorescent dye and quencher conjugations. Here, we describe a simplified method for rapid fluorescence detection of a target RNA using simple unmodified DNA oligonucleotides. To detect RNA, we developed Lettuce, a fluorogenic DNA aptamer that binds and activates the fluorescence of DFHBI-1T, an otherwise nonfluorescent molecule that resembles the chromophore found in green fluorescent protein. Lettuce was selected from a randomized DNA library based on binding to DFHBI-agarose. We further show that Lettuce can be split into two separate oligonucleotide components, which are nonfluorescent on their own but become fluorescent when their proximity is induced by a target RNA. We designed several pairs of split Lettuce fragments that contain an additional 15-20 nucleotides that are complementary to adjacent regions of the SARS-CoV-2 RNA, resulting in Lettuce fluorescence only in the presence of the viral RNA. Overall, these studies describe a simplified RNA detection approach using fully unmodified DNA oligonucleotides that reconstitute the Lettuce aptamer templated by RNA.

Deciphering the Role of Symmetry and Ligand Field in Designing Three-Coordinate Uranium and Plutonium Single-Molecule Magnets.

Actinide single-molecule magnets (SMMs) have gained paramount interest in molecular magnetism as they offer a larger barrier height of magnetization (Ueff) reversal compared to the lanthanide analogue, thanks to their greater metal-ligand covalency. However, the reported actinide SMMs to date yield a relatively smaller Ueff as there is no established design principle to enhance Ueff values. To address this issue, we have employed ab initio CASSCF/CASPT2/NEVPT2 calculations to study a series of three-coordinate U3+ and Pu3+ SMMs. To begin with, we have studied two experimentally characterized U3+ ion-field-induced SMMs, namely, planar [U{N(SiMe2tBu)2}3] (1) and pyramidal [U{N(SiMe3)2}3] (2) complexes reported earlier. Both the complexes were found to stabilize mJ = |±1/2⟩ as the ground state with a very strong quantum tunneling of magnetization (QTM), rendering them unsuitable for SMMs. Our calculations reveal that in the pyramidal geometry (such as in 2), the energy of the 5f26d1 state is lowered compared to the planar geometry (as in 1), resulting in a slightly better SMM characteristic in the former. To unravel the effect of symmetry in magnetic properties, ab initio calculations were performed on two reported T-shaped complexes [U(NSiiPr2)2(I)] (3) and [U(NHAriPr6)2I] (4, AriPr6 = 2,6-(2,4,6-iPr3C6H2)2C6H3). Quite interestingly, mJ = |±9/2⟩ is found to be the ground state for both the complexes with a blocking barrier exceeding 900 cm-1. Furthermore, to decipher the effect of the transuranic element in magnetic anisotropy, ab initio calculations were extended to the Pu analogue of 2, [Pu{N(SiMe3)2}3] (5), which yields a record-breaking blocking barrier of ∼1933 cm-1. Among the three-coordinate geometries studied, the pyramidal geometry was found to offer substantial magnetic anisotropy for Pu3+ ions, while a T-shaped geometry is best suited for U3+ ions. While the chosen theoretical protocols' overestimation of barrier height cannot be avoided, these values are still several orders of magnitude larger than the Ueff values reported for any actinide SMMs and unveil a design principle for superior three-coordinate actinide-based SMMs.

Deciphering the Role of Anions and Secondary Coordination Sphere in Tuning Anisotropy in Dy(III) Air-Stable D5h SIMs.

Precise control of the crystal field and symmetry around the paramagnetic spin centre has recently facilitated the engineering of high-temperature single-ion magnets (SIMs), the smallest possible units for future spin-based devices. In the present work, we report a series of air-stable seven coordinate Dy(III) SIMs {[L2 Dy(H2 O)5 ][X]3 ⋅L2 ⋅n(H2 O), n = 0, X = Cl (1), n=1, X = Br (2), I (3)} possessing pseudo-D5h symmetry or pentagonal bipyramidal coordination geometry with high anisotropy energy barrier (Ueff ) and blocking temperature (TB ). While the strong axial coordination from the sterically encumbered phosphonamide, t BuPO(NHi Pr)2 (L), increases the overall anisotropy of the system, the presence of high symmetry significantly quenches quantum tunnelling of magnetization, which is the prominent deactivating factor encountered in SIMs. The energy barrier (Ueff ) and the blocking temperature (TB ) decrease in the order 3>2>1 with the change of anions from larger iodide to smaller strongly hydrogen-bonded chloride in the secondary coordination sphere, albeit the local coordination geometry and the symmetry around the Dy(III) display only slight deviations. Ab initio CASSCF/RASSI-SO/SINGLE_ANISO calculations provide deeper insights into the dynamics of magnetic relaxation in addition to the role of the secondary coordination sphere in modulating the anisotropy of the D5h systems, using diverse models. Thus, in addition to the importance of the crystal field and the symmetry to obtain high-temperature SIMs, this study also probes the significance of the secondary coordination sphere that can be tailored to accomplish novel SIMs.

Repurposing an adenine riboswitch into a fluorogenic imaging and sensing tag.

Fluorogenic RNA aptamers are used to genetically encode fluorescent RNA and to construct RNA-based metabolite sensors. Unlike naturally occurring aptamers that efficiently fold and undergo metabolite-induced conformational changes, fluorogenic aptamers can exhibit poor folding, which limits their cellular fluorescence. To overcome this, we evolved a naturally occurring well-folded adenine riboswitch into a fluorogenic aptamer. We generated a library of roughly 1015 adenine aptamer-like RNAs in which the adenine-binding pocket was randomized for both size and sequence, and selected Squash, which binds and activates the fluorescence of green fluorescent protein-like fluorophores. Squash exhibits markedly improved in-cell folding and highly efficient metabolite-dependent folding when fused to a S-adenosylmethionine (SAM)-binding aptamer. A Squash-based ratiometric sensor achieved quantitative SAM measurements, revealed cell-to-cell heterogeneity in SAM levels and revealed metabolic origins of SAM. These studies show that the efficient folding of naturally occurring aptamers can be exploited to engineer well-folded cell-compatible fluorogenic aptamers and devices.

The fluorescent aptamer Squash extensively repurposes the adenine riboswitch fold.

Squash is an RNA aptamer that strongly activates the fluorescence of small-molecule analogs of the fluorophore of green fluorescent protein (GFP). Unlike other fluorogenic aptamers, isolated de novo from random-sequence RNA, Squash was evolved from the bacterial adenine riboswitch to leverage its optimized in vivo folding and stability. We now report the 2.7-Å resolution cocrystal structure of fluorophore-bound Squash, revealing that while the overall fold of the riboswitch is preserved, the architecture of the ligand-binding core is dramatically transformed. Unlike previously characterized aptamers that activate GFP-derived fluorophores, Squash does not harbor a G-quadruplex, sandwiching its fluorophore between a base triple and a noncanonical base quadruple in a largely apolar pocket. The expanded structural core of Squash allows it to recognize unnatural fluorophores that are larger than the simple purine ligand of the parental adenine riboswitch, and suggests that stable RNA scaffolds can tolerate larger variation than has hitherto been appreciated.