ID | 117782 |
Title Alternative | Preferred Conditions for SrtA Transpeptidation for Creating a DDS Tool
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Author |
Tabata, Atsushi
The University of Tokushima
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Anyoji, Natsuki
The University of Tokushima
Ohkubo, Yukimasa
The University of Tokushima
Tomoyasu, Toshifumi
The University of Tokushima
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Nagamune, Hideaki
The University of Tokushima
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Keywords | Sortase A
Staphylococcus aureus
drug-delivery system
liposome
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Content Type |
Journal Article
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Description | Background/Aim: This study aimed to determine the preferred conditions for the transpeptidase reaction of sortase A from Staphylococcus aureus, for the purpose of creating functional liposomes useful for a drug-delivery system (DDS). Materials and Methods: His-tagged recombinant sortase A with 59 amino acids deleted from the N-terminus (His-ΔN59SrtA) was prepared using an Escherichia coli expression system. The pH dependency and sorting signal sequence dependency of the transpeptidase reaction of His-ΔN59SrtA were analyzed by monitoring the transfer of model donor-substrates (i.e. His-tagged mutant green fluorescent proteins with a C-terminal LPxTG sorting signal) to model acceptor-beads with a GGGGGC peptide. In addition, using preferred conditions, the sortase A reaction was used to modify liposome surface. Results and Discussion: The transpeptidase reaction of His-ΔN59SrtA was enhanced under weakly acidic conditions. Transfer efficiency, based on sorting signal recognition by His-ΔN59SrtA, was similar to or higher than that obtained using several substrates with amino acids other than Glu in the sorting signal position “x”. Furthermore, liposomes containing GGGGGC peptide-linked dipalmitoylphosphatidylethanolamine were successfully modified using the preferred conditions for His-ΔN59SrtA determined in this study. Conclusion: Preferred conditions for the transpeptidase reaction of His-ΔN59SrtA, especially in a weakly acidic environment to enhance reaction, was established and successfully used to create functional liposomes applicable to DDS.
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Journal Title |
Anticancer Research
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ISSN | 02507005
17917530
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NCID | AA10625860
AA12440673
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Publisher | The International Institute of Anticancer Research
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Volume | 34
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Issue | 8
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Start Page | 4521
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End Page | 4527
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Published Date | 2014-07-29
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EDB ID | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
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TextVersion |
Publisher
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departments |
Bioscience and Bioindustry
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