TY - JOUR
T1 - Pyrazolone-Protein Interaction Enables Long-Term Retention Staining and Facile Artificial Biorecognition on Cell Membranes
AU - Xiong, Tao
AU - Chen, Yingchao
AU - Peng, Qiang
AU - Li, Mingle
AU - Lu, Sheng
AU - Chen, Xiaoqiang
AU - Fan, Jiangli
AU - Wang, Lei
AU - Peng, Xiaojun
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/8/28
Y1 - 2024/8/28
N2 - Cell membrane genetic engineering has been utilized to confer cell membranes with functionalities for diagnostic and therapeutic purposes but concerns over cost and variable modification results. Although nongenetic chemical modification and phospholipid insertion strategies are more convenient, they still face bottlenecks in either biosafety or stability of the modifications. Herein, we show that pyrazolone-bearing molecules can bind to proteins with high stability, which is mainly contributed to by the multiple interactions between pyrazolone and basic amino acids. This new binding model offers a simple and versatile noncovalent approach for cell membrane functionalization. By binding to cell membrane proteins, pyrazolone-bearing dyes enabled precise cell tracking in vitro (>96 h) and in vivo (>21 days) without interfering with the protein function or causing cell death. Furthermore, the convenient anchor of pyrazolone-bearing biotin on cell membranes rendered the biorecognition to avidin, showing the potential for artificially creating cell targetability.
AB - Cell membrane genetic engineering has been utilized to confer cell membranes with functionalities for diagnostic and therapeutic purposes but concerns over cost and variable modification results. Although nongenetic chemical modification and phospholipid insertion strategies are more convenient, they still face bottlenecks in either biosafety or stability of the modifications. Herein, we show that pyrazolone-bearing molecules can bind to proteins with high stability, which is mainly contributed to by the multiple interactions between pyrazolone and basic amino acids. This new binding model offers a simple and versatile noncovalent approach for cell membrane functionalization. By binding to cell membrane proteins, pyrazolone-bearing dyes enabled precise cell tracking in vitro (>96 h) and in vivo (>21 days) without interfering with the protein function or causing cell death. Furthermore, the convenient anchor of pyrazolone-bearing biotin on cell membranes rendered the biorecognition to avidin, showing the potential for artificially creating cell targetability.
UR - http://www.scopus.com/inward/record.url?scp=85201183708&partnerID=8YFLogxK
U2 - 10.1021/jacs.4c08987
DO - 10.1021/jacs.4c08987
M3 - 文章
C2 - 39138141
AN - SCOPUS:85201183708
SN - 0002-7863
VL - 146
SP - 24158
EP - 24166
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 34
ER -