Hiroaki Suga
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Hiroaki Suga has a total of 2 co-authors. Here are the top co-authors by number of shared publications:
- David R. W. Hodgson
Department of Chemistry, Durham University, South Road, Durham DH1 3LE, UK
1 shared publication Kristina M Smith
Department of Biological Sciences, University at Buffalo, State University of New York, Buffalo, New York 14260-3000, USA
1 shared publication
Latest Publications
- 24 November 2003
- Published by Wiley in Biopolymers
- Vol. 73 (1) , 130-150
Mechanistic studies on acyl‐transferase ribozymes and beyond
In vitro selection has allowed the isolation of many new ribozymes that are able to catalyze an ever‐widening array of chemical transformations. Mechanistic studies on these selected ribozymes have provided valuable insight into the methods that RNA can invoke to overcome different catalytic tasks. We focus on the methods employed in these mechanistic studies using the acyl‐transferase family of selected ribozymes as well‐studied reference systems. Chemical and biochemical techniques have been used in tandem in order to draw conclusions on the various modes of catalysis employed by the different family members. In turn, this type of mechanistic information may provide a means for the redesign and optimization of existing ribozymes or the basis for new selection systems for more powerful RNA catalysts. © 2003 Wiley Periodicals, Inc. Biopolymers 73: 130–150, 2004
- 24 November 2003
- Published by Wiley in Biopolymers
- Vol. 73 (1) , 130-150
Mechanistic studies on acyl‐transferase ribozymes and beyond
In vitro selection has allowed the isolation of many new ribozymes that are able to catalyze an ever‐widening array of chemical transformations. Mechanistic studies on these selected ribozymes have provided valuable insight into the methods that RNA can invoke to overcome different catalytic tasks. We focus on the methods employed in these mechanistic studies using the acyl‐transferase family of selected ribozymes as well‐studied reference systems. Chemical and biochemical techniques have been used in tandem in order to draw conclusions on the various modes of catalysis employed by the different family members. In turn, this type of mechanistic information may provide a means for the redesign and optimization of existing ribozymes or the basis for new selection systems for more powerful RNA catalysts. © 2003 Wiley Periodicals, Inc. Biopolymers 73: 130–150, 2004
- 1 October 2003
- Published by Elsevier in Current Opinion in Chemical Biology
- Vol. 7 (5) , 586-591
Molecular mechanisms of bacterial quorum sensing as a new drug target
- 1 October 2003
- Published by Elsevier in Current Opinion in Chemical Biology
- Vol. 7 (5) , 586-591
Molecular mechanisms of bacterial quorum sensing as a new drug target