Crucially, their blueprint may aid the design of better globomycin analogues and the exploration of thousands of other potential new antibiotic solutions to common but devastating infections.
Originally published by Trinity College Dublin
Editor’s Note: A portion of this work was conducted at the U.S. Department of Energy’s (DOE’s) Argonne National Laboratory at the Advanced Photon Source. X-ray crystallography provides a means to visualize atomic structures in detail, but growing well-ordered crystals of lipid-loving LspA required a special, turbid mix of components to be developed by the research team lead by Martin Caffrey. The cutting-edge advanced microcrystallography tools at the GM/CA beamline enabled the collection of high-quality diffraction data in the inhomogeneous samples of these tiny protein crystals. The GM/CA beamline is operated by Argonne Laboratory and funded by the National Institute of General Medical Sciences and the National Cancer Institute. GM/CA is a world leader for intense, tunable micro-beams for crystallography studies. The Advanced Photon Source is a DOE Office of Science User Facility.With antimicrobial resistance on the rise, the World Health Organization has advised that a post-antibiotic era, in which minor injuries and common infections could prove fatal, is looming. New drugs are badly needed.
Globomycin attracted attention as an antibacterial candidate of significant promise more than a decade ago because it inhibits a key enzyme LspA and thus the production of many cell wall proteins with critical roles in bacterial physiology, pathogenicity and antibiotic resistance. If delivered effectively, globomycin and globomycin-like drugs could knock out a variety of bacterial infections.
We are effectively drawing up battle plans to wage war against bacterial infections by borrowing from the arsenal of other bacteria.
However, the progression of earlier studies stagnated, partly because researchers did not possess the all-important high-resolution blueprints with which to guide further drug development. That hurdle has now been removed as that very blueprint has just been published in a landmark paper in leading international journal Science.
Professor of Membrane Structural and Functional Biology at Trinity College Dublin, Martin Caffrey, said: “Our LspA-globomycin blueprint can be used to inform the design of globomycin derivatives or analogues with improved binding, efficacy, selectivity and pharmacokinetic properties.”
“The molecular form of the complex makes it a suitable target with which to explore the thousands of inhibitors developed for other medically relevant aspartyl protease enzymes. These include drugs that treat high blood pressure and HIV AIDS.”
The blueprint might also be used to design entirely new drugs targeted specifically at the chemical constellation of the enzyme’s active site in the bacteria Pseudomonas aeruginosa. However, it may be that blueprints of LspA from other pathogenic bacterial species such as Enterococcus, Staphylococcus (MRSA), Klebsiella, Acinetobacter and Enterobacter should be the immediate focus of efforts at the design of species-specific antibiotic drugs.
Such so-called narrow spectrum antimicrobials are more attractive because they are less likely to promote a generalised antibiotic resistance response.
Professor Caffrey added: “What is especially exciting is that the blueprint makes it hard to conceive bacteria developing resistance to globomycin or newly developed analogues.”
“Globomycin and its enzyme target are networked to such a degree that any mutation perturbing the drug’s interaction would also likely impact on how the bacteria functions. Antibiotics that do not elicit resistance are invaluable to medicine, and this work might inspire the design of such drugs.”
In a twist of evolutionary fate, globomycin is a natural antimicrobial produced by bacteria of the Actinomycete type, which means we are effectively drawing up battle plans to wage war against bacterial infections by borrowing from the arsenal of other bacteria. Lessons in developing effective drugs should be learned from this reality.
This research was supported by Science Foundation Ireland.