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Qurat-ul-ain

Publications and source records attributed to Qurat-ul-ain.

3 recordsLinked to original sources

Inference-Time Projection for Physically Valid Biomolecular Diffusion Models

AlphaFold 3-style cofolding models predict biomolecular complexes with high structural accuracy, yet a large fraction of their outputs are physically invalid: chains overlap at interfaces, ligand bond lengths and angles are distorted, rings are non-planar, and stereocentres are inverted. Current approaches either steer the sampler with physics-informed potentials, which multiplies sampling cost and memory overhead making inference impossible on large complexes, or finetune the model, costing time and tying the fix to one architecture. We observe that, unlike structural accuracy, physical validity is fully verifiable at inference time from quantities the sampler already holds. We therefore treat physical validity as a constrained inference problem and introduce two closed-form projection operators applied to the diffusion model's denoised clean-coordinate estimate, $\hat{x}_0$: an inter-chain van der Waals projection that pushes apart the most severely clashing atom pairs, and a ligand distance-geometry projection that restores bond lengths, angles, internal contacts, planarity and chirality. Both operators are local, sparse and displacement-capped, require no network evaluations, gradients or importance sampling, and leave the denoiser and its weights untouched, so they can be dropped into any AF3-style sampler without retraining. Applied to two independently developed models, Boltz-2 and OpenFold-3, across five benchmarks (CASP15, CASP16, the PoseBusters monomer and complex sets, and the Boltz physical-validity test set), our method recovers perfect physical validity while preserving structural-accuracy and ligand-placement metrics. These gains are achieved with negligible runtime and memory overhead, providing a practical, model-agnostic route to physically valid all-atom structure prediction.

cs.AI↗

Microscopic Origin of Polarization-Controlled Magnetization Switching in FePt/BaTiO$_3$

Electric-field driven magnetization switching in FePt/BaTiO$_3$ (001) is demonstrated through first-principles calculations. The magnetic easy axis of FePt layer undergoes a transition from in-plane to perpendicular direction upon ferroelectric polarization reversal, a process sensitively controlled by epitaxial strain with threshold strain strain($η$) $η\approx\%$. At this phenomena, a large interfacial magnetoelectric coupling ($α_I = 3.6 \times 10^{-10}$ G$\cdot$cm$^2$/V) is responsible, stemming from the orbital reconstruction. In particular, the redistribution of Pt-$d$ orbital occupancy alters spin-orbit coupling, thereby tuning the competition between magnetic anisotropy ($K_i$) and magnetoelastic energy ($b_1$). Our work clarifies the fundamental physics of strain-engineered magnetoelectricity and suggests a concrete pathway for designing ultra-low-power voltage-controlled magnetic memory.

cond-mat.mtrl-sci↗

Enhanced voltage-controlled magnetic anisotropy via magneto-elasticity in FePt/MgO(001)

The interplay between magneto-electricity (ME) and magneto-elasticity (MEL) is studied in the context of voltage-controlled magnetic anisotropy (VCMA). Strain plays more than a role of changing lattice constant but that of the internal electric field in the heterostructure. As a prototype, FePt/MgO(001) is visited, where the behavior of two interfaces are drastically different: one exhibits switching the other does not. Whether an external electric field ($E_{ext}$) is present or not, we found VCMA coefficient larger than 1 pJ/V$\cdot$m, as a consequence of the rearrangement of $d$ orbitals with $m=\pm1$ and $\pm2$ in response to an external electric field. In addition, magneto-crystalline anisotropy (MA) is analyzed with strain taken into account, where non-linear feature is presented only accountable by invoking second-order MEL.

cond-mat.mtrl-sci↗