Hua Yue

Prof. Hua Yue

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 June 2011 in Biomacromolecules
Verified
Journal Article
Closed access
ZYZhan-Guo Yue
Zhan-Guo Yue
WWWei Wei
Wei Wei
PLPi-Ping Lv
Pi-Ping Lv
HYHua Yue
Hua Yue
LWLian-Yan Wang
Lian-Yan Wang
GMGuang-Hui Ma
Guang-Hui Ma

1 June 2012 in Biomaterials
Verified
Journal Article
Closed access
HYHua Yue
Hua Yue
WWWei Wei
Wei Wei
ZYZhanguo Yue
Zhanguo Yue
BWBin Wang
Bin Wang
NLNana Luo
Nana Luo
ZSZhiguo Su
Zhiguo Su

14 November 2019 in Nature Communications
Verified
Journal Article
Open access
PDF file
XWXiaoling Wu
Xiaoling Wu
HYHua Yue
Hua Yue
YZYuanyu Zhang
Yuanyu Zhang
XGXiaoyong Gao
Xiaoyong Gao
XLXiaoyang Li
Xiaoyang Li
JGJun Ge
Jun Ge
Enzymatic catalysis in living cells enables the in-situ detection of cellular metabolites in single cells, which could contribute to early diagnosis of diseases. In this study, enzyme is packaged in amorphous metal-organic frameworks (MOFs) via a one-pot co-precipitation process under ambient conditions, exhibiting 5–20 times higher apparent activity than when the enzyme is encapsulated in corresponding crystalline MOFs. Molecular simulation and cryo-electron tomography (Cryo-ET) combined with other techniques demonstrate that the mesopores generated in this disordered and fuzzy structure endow the packaged enzyme with high enzyme activity. The highly active glucose oxidase delivered by the amorphous MOF nanoparticles allows the noninvasive and facile measurement of glucose in single living cells, which can be used to distinguish between cancerous and normal cells.

4 January 2018 in Nature Materials
Verified
Journal Article
Closed access
PDF file
YXYufei Xia
Yufei Xia
JWJie Wu
Jie Wu
WWWei Wei
Wei Wei
YDYiqun Du
Yiqun Du
TWTao Wan
Tao Wan
GMGuanghui Ma
Guanghui Ma

4 July 2016 in Advanced Materials
Verified
Journal Article
Closed access
PDF file
KXKe Xiong
Ke Xiong
WWWei Wei
Wei Wei
YJYongjie Jin
Yongjie Jin
SWShumin Wang
Shumin Wang
DZDongxu Zhao
Dongxu Zhao
HXHai‐Yan Xie
Hai‐Yan Xie

24 February 2017 in Nature Communications
Verified
Journal Article
Open access
PDF file
NLNana Luo
Nana Luo
JWJeffrey K. Weber
Jeffrey K. Weber
SWShuang Wang
Shuang Wang
BLBinquan Luan
Binquan Luan
HYHua Yue
Hua Yue
Guanghui MaGuanghui Ma
Guanghui Ma
Engineered nanomaterials promise to transform medicine at the bio–nano interface. However, it is important to elucidate how synthetic nanomaterials interact with critical biological systems before such products can be safely utilized in humans. Past evidence suggests that polyethylene glycol-functionalized (PEGylated) nanomaterials are largely biocompatible and elicit less dramatic immune responses than their pristine counterparts. We here report results that contradict these findings. We find that PEGylated graphene oxide nanosheets (nGO-PEGs) stimulate potent cytokine responses in peritoneal macrophages, despite not being internalized. Atomistic molecular dynamics simulations support a mechanism by which nGO-PEGs preferentially adsorb onto and/or partially insert into cell membranes, thereby amplifying interactions with stimulatory surface receptors. Further experiments demonstrate that nGO-PEG indeed provokes cytokine secretion by enhancing integrin β8-related signalling pathways. The present results inform that surface passivation does not always prevent immunological reactions to 2D nanomaterials but also suggest applications for PEGylated nanomaterials wherein immune stimulation is desired.