TY - JOUR
T1 - A centrifugation-assisted peptide-mediated gene transfer method for high-throughput analyses
AU - Kimura, Mitsuhiro
AU - Yoshizumi, Takeshi
AU - Numata, Keiji
N1 - Funding Information:
The authors would like to thank Dr. Yutaka Kodama for providing the pGWB-35S: Nluc vector. This work was supported by JSPS KAKENHI Grant Number JP18K05638 to M. K., NEDO Grant to T. Y and ERATO Grant Number JPMJER1602 to K. N.
Publisher Copyright:
© 2019 The Japanese Society for Plant Cell and Molecular Biology.
PY - 2019
Y1 - 2019
N2 - A peptide-mediated DNA delivery system for several plant species has been recently developed. This system uses ionic complexes of DNA and fusion peptides containing several domains, such as DNA-binding and cell-penetrating peptides. Although the peptide-DNA complexes are capable of penetrating into plant cells through the cell wall by mechanical pressure using a syringe, sample throughput is limited. Here, we describe a Centrifugation-Assisted Peptide-mediated gene Transfer (CAPT) method for improving sample throughput with reproducible gene transfer efficiency. We optimized the parameters of CAPT for transient gene transfer efficiency by using Nicotiana tabacum cotyledons as a model plant material. The optimal parameters for centrifugation were 10,000×g for 60 s. Furthermore, we successfully transferred the peptide–DNA complex into rice cotyledons using the optimized CAPT method. Thus, the CAPT method is superior to the previous syringe-mediated infiltration method in terms of sample throughput in multiple plant species.
AB - A peptide-mediated DNA delivery system for several plant species has been recently developed. This system uses ionic complexes of DNA and fusion peptides containing several domains, such as DNA-binding and cell-penetrating peptides. Although the peptide-DNA complexes are capable of penetrating into plant cells through the cell wall by mechanical pressure using a syringe, sample throughput is limited. Here, we describe a Centrifugation-Assisted Peptide-mediated gene Transfer (CAPT) method for improving sample throughput with reproducible gene transfer efficiency. We optimized the parameters of CAPT for transient gene transfer efficiency by using Nicotiana tabacum cotyledons as a model plant material. The optimal parameters for centrifugation were 10,000×g for 60 s. Furthermore, we successfully transferred the peptide–DNA complex into rice cotyledons using the optimized CAPT method. Thus, the CAPT method is superior to the previous syringe-mediated infiltration method in terms of sample throughput in multiple plant species.
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U2 - 10.5511/plantbiotechnology.18.1115a
DO - 10.5511/plantbiotechnology.18.1115a
M3 - Comment/debate
AN - SCOPUS:85065920654
SN - 1342-4580
VL - 36
SP - 49
EP - 52
JO - Plant Biotechnology
JF - Plant Biotechnology
IS - 1
ER -