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| 1 | An efficient two-step subcellular fractionation method for the enrichment of insulin granules from INS-1 cells显示文摘 | Yan Chen Zhiping Xia Lifen Wang Yong Yu Pingsheng Liu Eli Song Tao Xu | 2015 | Biophysics Reports2015，1，1： | 2 |
| 2 | , Near- infrared Lumine-scence of OH-Cl-Doped Bi4Ge3O12 crystals 显示文摘 | Yu Pingsheng Su Liangbi Zhao Hengyu | 2012 | Infrared Physics & Technology2012，55，： | 1 |
| 3 | Phosphorylation and function of DGAT1 in skeletal muscle cells显示文摘 | Jinhai Yu Yiran Li Fei Zou Shimeng Xu Pingsheng Liu | 2015 | Biophysics Reports2015，1，1： | 1 |
| 4 | HID-1 is a peripheral membrane protein primarily associated with the medial-and transGolgi apparatus显示文摘Caenorhabditis elegans hid-1 gene was first identified in a screen for mutants with a high-temperature-induced dauer formation(Hid)phenotype.Despite the fact that the hid-1 gene encodes a novel protein(HID-1)which is highly conserved from Caenorhabditis elegans to mammals,the domain structure,subcellular localization,and exact function of HID-1 remain unknown.Previous studies and various bioinformatic softwares predicted that HID-1 contained many transmembrane domains but no known functional domain.In this study,we revealed that mammalian HID-1 localized to the medial-and transGolgi apparatus as well as the cytosol,and the localization was sensitive to brefeldin A treatment.Next,we demonstrated that HID-1 was a peripheral membrane protein and dynamically shuttled between the Golgi apparatus and the cytosol.Finally,we verified that a conserved N-terminal myristoylation site was required for HID-1 binding to the Golgi apparatus.We propose that HID-1 is probably involved in the intracellular trafficking within the Golgi region. | Lifen Wang Yi Zhan Eli Song Yong Yu Yaming Jiu Wen Du Jingze Lu Pingsheng Liu Pingyong Xu Tao Xu | 2011 | Protein & Cell2011，2，1： | 1 |
| 5 | Study on photoluminescence of thermally treated Bi_(12)GeO_(20) and Mo:Bi_(12)GeO_(20) crystals显示文摘Photoluminescence (PL) of Bi12GeO20 and Mo doped Bi12GeO20 (Mo: Bi12GeO20) crystals in visible and near-infrared (NIR) spectral regions were studied. X-ray diffraction analysis, absorption and Raman scattering spectra of these crystals were also measured. Pure Bi12GeO20 after annealing in N2 atmosphere at 450 oC and 550 °C show predominant emissions at about 745 and 1250 nm bands, while the emission peaks of Mo:Bi12GeO20 crystals untreated or after annealing in Ar at 300 °C are at around 538 and 1165 nm. The results suggest that annealing induces intrinsic luminescence of Bi in pure Bi12GeO20 at room temperature and Mo influences the luminescence centers of Bi12GeO20. The emission peaks of Bi12GeO20 and Mo: Bi12GeO20 probably owe to lower-valent Bi ions. | YU PingSheng SU LiangBi TANG HuiLi GUO Xin ZHAO HengYu YANG QiuHong XU Jun | 2011 | Science China(Technological Sciences)2011，54，5： | 1 |
| 6 | Perilipin 2 and lipid droplets provide reciprocal stabilization显示文摘The lipid droplet (LD)-associated protein adipose differentiation-related protein (ADRP or PLIN2) is required for the formation and stability of the LD organelle, whereas its biological roles are still obscure. Herein, we show that PLIN2 is the most abundant protein on the lipid droplets (LDs) of mouse myoblast cell line C2C12. Both the expression of PLIN2 and the accumulation of LDs were up-regulated in a time- and dose-dependent manner when the cells were treated with oleate (OA). The protein level of PLIN2 was positively correlated with the formation of LDs, suggesting that LDs stabilize PLIN2. Furthermore, knocking out PLIN2 in C2C12 cells led to enlarged LDs and higher triacylglycerol hydrolysis activity. The isolated PLIN2 null LDs became closely contact w让h mitochondria and other cellular organelles. Additionally mitochondrial activity was suppressed by OA in PLIN2 null cells. Our results reveal the pivotal roles of PLIN2 in governing LD dynamics and their relationship to mitochondria, and suggest a reciprocal stabilization between PLIN2 and LDs. | Shimeng Xu Fei Zou Zhiqing Diao Shuyan Zhang Yaqin Deng Xiaotong Zhu Liujuan Cui Jinhai Yu Zhiguang Zhang Adekunle Toyin Bamigbade Hongchao Zhang Xuan Wei Xuelin Zhang Bin Liang Pingsheng Liu | 2019 | Biophysics Reports2019，5，3： | 1 |
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