Drug intelligence / Profile preview

LysPSPa-IDR-1018

Development stage
Preclinical
Lead developer
Alagappa University
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Peptides
Administration
Topical
01

Overview

LysPSPa-IDR-1018 is an engineered fusion endolysin developed by researchers at Alagappa University for the treatment of diabetic foot ulcers (DFUs). It is created by integrating the synthetic immunomodulatory peptide IDR-1018 with the PSPa phage-encoded endolysin (LysPSPa). LysPSPa-IDR-1018 exhibits a dual mechanism of action: it exerts potent bactericidal and biofilm-disrupting activity against multidrug-resistant (MDR) pathogens, including methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli, and Pseudomonas aeruginosa, while simultaneously promoting wound healing and immunomodulation. In preclinical studies, the fusion protein demonstrated significant wound-healing potential in human gingival fibroblasts and enhanced cell migration, accompanied by elevated expression of interleukin-10 (IL-10) and tumor necrosis factor-alpha (TNF-α) in macrophage cells.

02

Targets

PGN (Peptidoglycan)ppGpp (Guanosine pentaphosphate)

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