# Preparation and application of Taq DNA polymerase monoclonal antibody guided by structural domain analysis

## TL;DR

This paper introduces a new method to create a hot-start Taq DNA polymerase using monoclonal antibodies, improving PCR accuracy and efficiency.

## Contribution

A structure-guided, domain-specific immunization strategy for generating monoclonal antibodies against Taq DNA polymerase.

## Key findings

- The monoclonal antibody effectively blocks Taq activity at room temperature and releases it upon heating.
- The resulting hot-start Taq reduced non-specific amplification in PCR assays.
- The method was successfully applied to detect pathogens in clinical samples.

## Abstract

Hot-start polymerase chain reaction (hot-start PCR) effectively inhibits non-specific product amplification during PCR, with hot-start Taq DNA polymerase (HS Taq) serving as the critical component. Current HS Taq preparation methods, including chemical modification and aptamer-based approaches, exhibit limitations such as prolonged activation time, reduced enzyme activity, and inadequate blocking specificity. In contrast, antibody-mediated hot-start Taq offers distinct advantages: rapid activation, stable enzymatic performance, and high blocking specificity through targeted binding to functional domains. While antibody-based hot-start Taq DNA polymerases are widely utilized for their high efficiency and specificity, their development often relies on commercial sources or complex genetic engineering. This dependency constrains the independent and customizable development of core PCR components. To address this, our study established a streamlined platform for generating highly effective monoclonal antibodies that inhibit Taq enzyme activity. The key innovation lies in our structure-guided, domain-specific immunization strategy: instead of using the full-length enzyme, we targeted the polymerase domain (Taq-P) to generate a specific monoclonal antibody that acts as a reversible inhibitor. This approach overcomes the major challenge of generating functional antibodies against cryptic epitopes, which are poorly immunogenic in the full-length protein. This antibody sterically blocks the enzyme’s active site at room temperature, preventing non-specific priming during PCR setup, and dissociates upon thermal activation to restore full activity. The resulting hot-start Taq enzyme significantly reduced non-specific amplification in quantitative PCR assays, and its practical utility was successfully demonstrated in detecting fungal pathogens and respiratory viruses using clinical samples. This study provides a feasible and effective strategy for the autonomous development of critical reagents for molecular diagnostics.