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The nature of the highly efficient energy transfer in photosynthetic light-harvesting complexes is a subject of intense research.
The use of metal-organic complexes is a potentially fruitful approach for the development of novel enzyme inhibitors.
The design of biocompatible polyelectrolyte complexes is a promising strategy for in vivo delivery of biologically active macromolecules.
Revealing the atomistic architecture of supramolecular complexes is a fundamental step toward a deeper understanding of cellular functioning.
Iron uptake via endocytosis of iron-transferrin-transferrin receptor complexes is a rate-limiting step for cell growth, viability and proliferation in tumor cells as well as non-transformed cells such as activated lymphocytes.
"It's much easier to turn off the signal than turn it on," Hurley says, and the effort to do so by changing the conformation of the two protein complexes is a young field made possible by powerful structural imaging techniques.
Selection of a suitable substrate for special pigment-protein complexes is a significant challenge for building an inexpensive and efficient device.
Biochemical and in silico studies give grounds that the biological activity of dinitrosyl iron complexes is a μ-SR bridging ligand structure function.
The internal geometry of the channel complexes is a result of a complex interaction between lateral confinement, by-pass and lateral migration processes.
Another reason for the limited stability of alkyl ligands in many d-block complexes is a set of reactions that can be quite rapid, such as β-hydrogen elimination, CO insertion, and reductive elimination.
The redox potential of macrocyclic complexes is a very predictive reactivity index for the electrocatalytic activity of these molecules and it can be easily measured under the same conditions of the kinetic experiments.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com