An integrated platform for the capture of circulating tumor cells and: In situ SERS profiling of membrane proteins through rational spatial organization of multi-functional cyclic RGD nanopatterns

Hui Dong; Dazhi Yao; Qi Zhou; Limin Zhang; Yang Tian

doi:10.1039/c8cc09108k

An integrated platform for the capture of circulating tumor cells and: In situ SERS profiling of membrane proteins through rational spatial organization of multi-functional cyclic RGD nanopatterns

Hui Dong
, Dazhi Yao
, Qi Zhou
, Limin Zhang^*
, Yang Tian

^*Corresponding author for this work

School of Chemistry and Molecular Engineering

East China Normal University

Research output: Contribution to journal › Article › peer-review

22 Scopus citations

Abstract

It is significant to in situ monitor membrane proteins at the single-cell level for understanding the cell function. Herein, an integrated platform was designed and constructed for highly efficient cell capture and in situ sensitive SERS determination of HER2 activity in cells through rational spatial organization of multi-functional cyclic RGD nanopatterns at a disordered mesoporous gold film via electrochemical activation.

Original language	English
Pages (from-to)	1730-1733
Number of pages	4
Journal	Chemical Communications
Volume	55
Issue number	12
DOIs	https://doi.org/10.1039/c8cc09108k
State	Published - 2019

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10.1039/c8cc09108k

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title = "An integrated platform for the capture of circulating tumor cells and: In situ SERS profiling of membrane proteins through rational spatial organization of multi-functional cyclic RGD nanopatterns",

abstract = "It is significant to in situ monitor membrane proteins at the single-cell level for understanding the cell function. Herein, an integrated platform was designed and constructed for highly efficient cell capture and in situ sensitive SERS determination of HER2 activity in cells through rational spatial organization of multi-functional cyclic RGD nanopatterns at a disordered mesoporous gold film via electrochemical activation.",

author = "Hui Dong and Dazhi Yao and Qi Zhou and Limin Zhang and Yang Tian",

note = "Publisher Copyright: {\textcopyright} 2019 The Royal Society of Chemistry.",

year = "2019",

doi = "10.1039/c8cc09108k",

language = "英语",

volume = "55",

pages = "1730--1733",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

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An integrated platform for the capture of circulating tumor cells and: In situ SERS profiling of membrane proteins through rational spatial organization of multi-functional cyclic RGD nanopatterns. / Dong, Hui; Yao, Dazhi; Zhou, Qi et al.
In: Chemical Communications, Vol. 55, No. 12, 2019, p. 1730-1733.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - An integrated platform for the capture of circulating tumor cells and

T2 - In situ SERS profiling of membrane proteins through rational spatial organization of multi-functional cyclic RGD nanopatterns

AU - Dong, Hui

AU - Yao, Dazhi

AU - Zhou, Qi

AU - Zhang, Limin

AU - Tian, Yang

PY - 2019

Y1 - 2019

N2 - It is significant to in situ monitor membrane proteins at the single-cell level for understanding the cell function. Herein, an integrated platform was designed and constructed for highly efficient cell capture and in situ sensitive SERS determination of HER2 activity in cells through rational spatial organization of multi-functional cyclic RGD nanopatterns at a disordered mesoporous gold film via electrochemical activation.

AB - It is significant to in situ monitor membrane proteins at the single-cell level for understanding the cell function. Herein, an integrated platform was designed and constructed for highly efficient cell capture and in situ sensitive SERS determination of HER2 activity in cells through rational spatial organization of multi-functional cyclic RGD nanopatterns at a disordered mesoporous gold film via electrochemical activation.

UR - https://www.scopus.com/pages/publications/85061121681

U2 - 10.1039/c8cc09108k

DO - 10.1039/c8cc09108k

M3 - 文章

C2 - 30657476

AN - SCOPUS:85061121681

SN - 1359-7345

VL - 55

SP - 1730

EP - 1733

JO - Chemical Communications

JF - Chemical Communications

IS - 12

ER -

An integrated platform for the capture of circulating tumor cells and: In situ SERS profiling of membrane proteins through rational spatial organization of multi-functional cyclic RGD nanopatterns

Abstract

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