T. Kigawa

Systems Biology Institute

Papers

2

Total Citations

66

H-Index

2

About

T. Kigawa has made transformative contributions to structural and functional genomics through pioneering work in cell-free protein synthesis systems. His primary research focuses on high-throughput protein production methodologies, particularly the development of automated, cell-free expression platforms that bypass traditional cloning bottlenecks. Kigawa’s landmark 2009 paper on the “Automated system for high-throughput protein production using the dialysis cell-free method” has garnered 64 citations, reflecting its foundational role in enabling rapid, scalable protein synthesis for structural biology. He further advanced the field by demonstrating how bacterial cell-free systems, combined with a two-step PCR approach using linear DNA templates, eliminate time-consuming cloning steps—a breakthrough that accelerates functional analysis of proteins. This work has been instrumental in large-scale projects like structural genomics initiatives, where speed and reproducibility are critical. Kigawa’s innovations have empowered researchers to produce difficult-to-express proteins, including membrane proteins and complexes, opening new avenues for drug discovery and proteomics. His contributions remain a cornerstone for labs seeking efficient, cost-effective protein production, cementing his legacy as a key architect of modern cell-free biotechnology.

Research Focus

Key Achievements

2
H-Index
2
Papers
66
Total Citations
33
Avg Citations/Paper
🏆 Most Cited Paper
Automated system for high-throughput protein production using the dialysis cell-free method
64 citations · 2009
📈 Most Prolific Year: 2009 (2 Papers)
🤝 Key Collaborators: 6
🏛 Institutions: Systems Biology Institute

Top Papers

  1. 1
  2. 2

Key Collaborators

Contact & Links

Available for collaboration
Content generated · 15 days ago