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The role of linker on the elevated biosensing performance of a carbohydrate-binding module-tagged sarcosine oxidase
Yi Yu1, Xiaozhen Huang1, Furui Yang1
1Biology Institute, Qilu University of Technology (Shandong Academy of Sciences), No. 28789, Jingshi East Road, Licheng District, Jinan, Shandong, 250103, China.
Abstract:
Creatinine is a pivotal biomarker for renal function assessment, and developing its rapid, sensitive, stable point-of-care testing (POCT) biosensors remains critical. Enzyme-based biosensors using sarcosine oxidase (SOX) in a three-enzyme cascade are promising, but challenges persist in post-immobilization enzymatic activity and long-term stability, especially for low-activity SOX. Herein, we report rational engineering of carbohydrate-binding module 3 (CBM3)-fused SOX variants to address these limitations. CBM3 was genetically fused to N-/C-termini of monomeric SOX via distinct linkers (proline-rich XP for N-terminal, α-helical EAAK for C-terminal), generating CBM3-XP-SOX and SOX-EAAK-CBM3. Comparative analysis showed SOX-EAAK-CBM3 exhibited superior soluble expression (15.96 mg/mL), enhanced ambient-temperature catalytic activity (39.96%-56.23% higher than WT SOX), and exceptional electrochemical stability (25 days, R2 > 0.99). In contrast, CBM3-XP-SOX suffered linker cleavage and structural instability, limiting stability to 2 days. Structure-guided linker engineering of the N-terminal fusion identified unstable K-E-P motif in XP linker; truncation and flexible glycine introduction yielded CBM3-XG-SOX. The CBM3-XG-SOX/cellulose/Pt biosensor showed 7-fold improved electrochemical stability (15 days) vs. parental CBM3-XP-SOX, with rapid response (19-30 s) and strong anti-interference against physiological interferents. Serum and urine real-sample analysis confirmed high accuracy (recovery: 96.28%-97.88%) and superior precision vs. commercial kits, with narrower errors for low or high creatinine concentrations. This work establishes a rational framework for fusion enzyme engineering via bioinformatics-guided linker/fusion site optimization, overcoming low-activity enzyme-based biosensor limitations. CBM3-fused SOX biosensors enable cost-effective, stable, sensitive POCT creatinine detection, with broad clinical diagnosis and home health monitoring applications.
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