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71.
应用噬菌体抗体库技术制备全人源抗滋养层细胞表面抗原-2(Trop-2)特异性Fab抗体片段.抗体库经细胞筛选和固相抗原筛选,获得特异性的阳性克隆.阳性载体经核酸序列分析后,构建工程菌,经IPTG诱导表达,SDS-PAGE和Western blot分析,呈现28 ku和32 ku大小的两条蛋白质条带.Fab分子经流式细胞术、细胞免疫荧光检测,结果表明,Fab能够与BxPc3细胞膜蛋白特异性结合,而与NIH3T3细胞不结合.免疫共沉淀与质谱分析结果表明,该Fab分子能够与Trop-2蛋白特异性结合.免疫组化显示,该抗体可结合胰腺癌细胞膜蛋白,在细胞培养液中加入Fab,能够抑制BxPc3细胞的生长.以上研究结果提示,该抗体有望成为胰腺癌临床影像诊断或治疗的候选分子. 相似文献
72.
Yoon-Jeong Park Jin Chang Pen-Chung Chen Victor Chi-Min Yang 《Biotechnology and Bioprocess Engineering》2001,6(5):326-331
With the aim of developing a pH-sensitive controlled drug release system, a poly (L-lysine) (PLL) based cationic semi-interpenetrating polymer network (semi-IPN) has been synthesized. This cationic hydrogel
was designed to swell at lower pH and de-swell at higher pH and therefore be applicable for achieving regulated drug release
at a specific pH range. In addition to the pH sensitivity, this hydrogel was anticipated to interact with an ionic drug, providing
another means to regulate the release rate of ionic drugs. This semi-IPN hydrogel was prepared using a free-radical polymerization
method and by crosslinking of the polyethylene glycol (PEG)-methacrylate polymer through the PLL network. The two polymers
were penetrated with each other via interpolymer complexation to yield the semi-IPN structures. The PLL hydrogel thus prepared
showed dynamic swelling/de-swelling behavior in response to pH change, and such a behavior was influenced by both the concentrations
of PLL and PEG-methacrylate. Drug release from this semi-IPN hydrogel was also investigated using a model protein drug, streptokinase.
Streptokinase release was found to be dependent on its ionic interaction with the PLL backbones as well as on the swelling
of the semi-IPN hydrogel. These results suggest that a PLL semi-IPN hydrogel could potentially be used as a drug delivery
platform to modulate drug release by pH-sensitivity and ionic interaction. 相似文献
73.
74.
An Appropriate Cutoff Value for Determining the Colonization of Helicobacter pylori by the Pyrosequencing Method: Comparison with Conventional Methods 下载免费PDF全文
75.
Se Ryun Kwon Yue Jai Kang Dong Jin Lee Eun Hye Lee Yoon Kwon Nam Sung Koo Kim Ki Hong Kim 《Molecular biotechnology》2009,42(2):154-159
Vibrio anguillarum ghosts (VAG) were generated, for the first time, using a conjugation vector containing a ghost bacteria inducing cassette,
pRK-λPR-cI-Elysis, in which the expression of PhiX174 lysis gene E was controlled by the P
R
/cI regulatory system of lambda phage. By scanning electron microscopy, holes ranging 80–200 nm in diameter were observed in
the VAG. To avoid the presence of bacterial genomic DNA and an antibiotic resistance gene in the final VAG product, we constructed
a new dual vector, pRK-λPR-cI-E-SNA, containing the E-mediated lysis cassette and the staphylococcal nuclease A (SNA)-mediated DNA degradation cassette, and generated safety-enhanced VAG for use as a fish vaccine. 相似文献
76.
77.
Jin SM Lazarou M Wang C Kane LA Narendra DP Youle RJ 《The Journal of cell biology》2010,191(5):933-942
PINK1 is a mitochondrial kinase mutated in some familial cases of Parkinson's disease. It has been found to work in the same pathway as the E3 ligase Parkin in the maintenance of flight muscles and dopaminergic neurons in Drosophila melanogaster and to recruit cytosolic Parkin to mitochondria to mediate mitophagy in mammalian cells. Although PINK1 has a predicted mitochondrial import sequence, its cellular and submitochondrial localization remains unclear in part because it is rapidly degraded. In this study, we report that the mitochondrial inner membrane rhomboid protease presenilin-associated rhomboid-like protein (PARL) mediates cleavage of PINK1 dependent on mitochondrial membrane potential. In the absence of PARL, the constitutive degradation of PINK1 is inhibited, stabilizing a 60-kD form inside mitochondria. When mitochondrial membrane potential is dissipated, PINK1 accumulates as a 63-kD full-length form on the outer mitochondrial membrane, where it can recruit Parkin to impaired mitochondria. Thus, differential localization to the inner and outer mitochondrial membranes appears to regulate PINK1 stability and function. 相似文献
78.
渗透胁迫调节的转基因表达对植物抗旱耐盐性的影响 总被引:29,自引:0,他引:29
干旱和盐渍是影响植物生长和农作物产量的最重要的环境因子,本文综述了近年来通过超量表达低分子量化合物和渗透肋迫保护蛋白等获得抗旱耐盐转基因植物的报道,旨在系统阐述转基因表达对植物抗旱耐盐性的影响。 相似文献
79.
Jin‐Young Lee Hahyun Park Whasun Lim Gwonhwa Song 《Journal of cellular physiology》2021,236(2):1545-1558
The therapeutic potential of α,β‐thujone, a functional compound found in many medicinal plants of the Cupressaceae, Asteraceae, and Lamiaceae families, has been demonstrated, including in inflammation and cancers. However, its pharmacological functions and mechanisms of action in ovarian cancer remain unclear. We investigated the anticancer properties of α,β‐thujone in ES2 and OV90 human ovarian cancer cells and its effect on sensitization to cisplatin. α,β‐thujone inhibited cancer cell proliferation and induced cell death through caspase‐dependent intrinsic apoptotic pathways. Moreover, α,β‐thujone‐mediated endoplasmic reticulum stress was associated with the loss of mitochondrial functions and altered metabolic landscape of ovarian cancer cells. α,β‐Thujone attenuated blood vessel formation in transgenic zebrafish, implying it has significant antiangiogenic potential. In addition, α,β‐thujone sensitized ovarian cancer cells to cisplatin, causing synergistic pharmacological effects. Collectively, our results suggest that α,β‐thujone has therapeutic potential in human ovarian cancer and functions via regulating multiple intracellular stress‐associated metabolic reprogramming and caspase‐dependent apoptotic pathways. 相似文献
80.