An automated fiber-optic SPR platform with a self-assembled peptide interface for sPD-L1 analysis

An automated FO-SPR method is established for sPD-L1 quantification. • The EMP interface self-assembles on FO-probes via terminal cysteines. • The functionalized probes retained > 90% of their initial response after 4 weeks at 4 °C. • sPD-L1 detection is achieved in diluted human serum via Ab-AuNP amplification. An automated dip-probe fiber-optic surface plasmon resonance (FO-SPR) method was developed for soluble programmed death-ligand 1 (sPD-L1) quantification. The system employs a one-step self-assembled epitope-mimicking peptide (EMP) as the capture element. Through a terminal cysteine, the EMP binds directly onto the gold probe to form a capture interface, eliminating the need for chemical cross-linking. Coupled with an antibody-conjugated gold nanoparticle (Ab-AuNP) sandwich assay, the FO-SPR platform achieved a limit of detection of 20.5 ng/mL in diluted human serum with recoveries ranging from 93.7% to 106.6%. Independently prepared probes yielded intra- and inter-assay relative standard deviations below 6%, and EMP-functionalized probes retained more than 90% of their initial response after four weeks of storage at 4 °C. By pairing this peptide interface with a direct-immersion format that avoids fluidic clogging, this work delivers a practical and automated FO-SPR methodology for diverse bioanalytical applications. Download: Download high-res image (122KB) Download: Download full-size image