Labeled TEMPO-Oxidized Mannan Differentiates Binding Profiles within the Collectin Families

Establishing the rapid and accurate diagnosis of sepsis is a key component to the improvement of clinical outcomes. The ability of analytical platforms to rapidly detect pathogen-associated molecular patterns (PAMP) in blood could provide a powerful host-independent biomarker of sepsis. A novel concept was investigated based on the idea that a pre-bound and fluorescent ligand could be released from lectins in contact with high-affinity ligands (such as PAMPs). To create fluorescent ligands with precise avidity, the kinetically followed TEMPO oxidation of yeast mannan and carbodiimide coupling were used. The chemical modifications led to decreases in avidity between mannan and human collectins, such as the mannan-binding lectin (MBL) and human surfactant protein D (SP-D), but not in porcine SP-D. Despite this effect, these fluorescent derivatives were captured by human lectins using highly concentrated solutions. The resulting fluorescent beads were exposed to different solutions, and the results showed that displacements occur in contact with higher affinity ligands, proving that two-stage competition processes can occur in collectin carbohydrate recognition mechanisms. Moreover, the fluorescence loss depends on the discrepancy between the respective avidities of the recognized ligand and the fluorescent mannan. Chemically modulated fluorescent ligands associated with a diversity of collectins may lead to the creation of diagnostic tools suitable for multiplex array assays and the identification of high-avidity ligands.

Automated summary

Establishing rapid and accurate diagnosis of sepsis is crucial for improving clinical outcomes. Analytical platforms that can quickly detect pathogen-associated molecular patterns (PAMPs) in blood offer a powerful host-independent biomarker for sepsis. This study investigated a novel concept of using pre-bound and fluorescent ligands released from lectins in contact with high-affinity ligands to create precise avidity fluorescent ligands. Chemical modifications of these ligands showed differences in their interactions with mannan-binding lectin (MBL) and human surfactant protein D (SP-D), indicating the potential for diagnostic tool development.