TAN Xiaotian, LI Ruihan, YANG Hui. Antibody probes in biomolecular sensing: from carbon-based computing to silicon-based computing[J]. Synthetic Biology Journal, 2026, 7(1): 93-101
TAN Xiaotian, LI Ruihan, YANG Hui. Antibody probes in biomolecular sensing: from carbon-based computing to silicon-based computing[J]. Synthetic Biology Journal, 2026, 7(1): 93-101 DOI: 10.12211/2096-8280.2024-085.
Antibody probes in biomolecular sensing: from carbon-based computing to silicon-based computing封面论文
and analysis of protein biomarkers are essential for disease diagnosis and life sciences research. Antibody probes
known for their high specificity and stability
are crucial to biomolecular sensing assays. Traditionally
antibody development has relied on “carbon-based” approaches using animal immune systems. However
we are currently undergoing a transformative shift toward “silicon-based” methods driven by artificial intelligence (AI). Conv
entional techniques
such as animal-based antibody production and phage display-based directed evolution
have long been challenged by low efficiency and limited control over epitope specificity and binding affinity. Recent AI advances
including
de
novo
protein design and deep learning-driven protein binding protein (PBP) generation
are revolutionizing antibody development. These innovations enable the rapid creation of protein-based biosensing probes (
e.g.
antibodies and nanobodies) with enhanced specificity and affinity
along with accurate predictions of epitopes and structural features. By overcoming limitations with traditional methods
AI-driven technologies offer unprecedented control over the design and performance of antibody probes. Furthermore
“silicon-based evaluation” plays a key role in PBP generation
allowing for quantitative assessment of binding affinity
stability
and robustness. AI-designed biosensing probes offer potentials for capturing a broader spectrum of biomolecular information
which may be able to detect variations in sequence and conformation
post-translational modifications
abnormal polymerization
and shifts in biological activity. In certain diseases
the abnormal dissociation of multimeric proteins can reveal previously concealed antigenic epitopes
creating disease-specific targets
which can be better addressed with AI-designed probes for more accurate and nuanced insights. Moreover
modern high-performance biomolecular sensing technologies
such as bead-based chemiluminescent immunoassays (CLIA)
digital immunoassay
microfluidic immunoassay
and single molecule binding kinetics assays
require highly diverse antibody specificity and affinity
and AI-based protein design tools can meet these divergent needs
enabling the integration of AI-engineered biosensing probes with next-generation sensors. This integration not only enhances detection sensitivity
but also expands the scope of molecular information that can be ana
lyzed. Such a paradigm shift represents a new era in biomolecular sensing
and offers exciting prospects for precision medicine and synthetic biology.
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references
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