I . Screening of Vibrio harveyi-Binding Peptide Aptamers II.
与哈威弧菌结合之多胜肽；适合体之筛选II。
This study utilized purified IBV H52 strain to screen specific virus-binding peptides from Ph. D. -12TM phage display peptide library.
本研究使用纯化的鸡传染性支气管炎病毒（IBV），从12肽噬菌体展示随机肽库中筛选特异性结合多肽。
Objective To investigate the effect of resistin and resistin binding peptide(RBP) on the glucose uptake in L6 rat skeletal muscle cells.
目的探讨抵抗素及其结合多肽（RBP）对大鼠骨骼肌细胞糖摄取功能的影响。
Angiotensin - (1-7) is a small peptide that binds to proteins on the surface of cells and prevents cell growth - but only if the cell is actively growing when the binding occurs.
血管紧张素-(1 - 7)是一种能连接到细胞膜表面蛋白的小肽，仅当细胞活跃的生长时，这种小肽与表面蛋白结合后即能阻止细胞的生长。
This peptide is the natural binding partner for it.
多肽是天然约束细菌的助手。
METHODS: Using CHO cells which high express human CD59 as target cells, the phage 12 peptide library was screened for 5 rounds by competitive binding test.
方法：以高表达人CD59的中国仓鼠卵巢细胞（CHO）为靶细胞，采用竞争结合试验，对噬菌体随机12肽库进行5轮亲和筛选。
Objective: to select the peptide binding to influenza virus neuraminidase from phage display 12 peptide library.
目的：从噬菌体呈现12肽库中筛选与流感病毒神经氨酸酶特异性结合的肽。
The binding ability of new peptide ligand GE11 and epidermal growth factor receptor (EGFR) was analyzed by affinity capillary electrophoresis (ACE) method.
应用亲和毛细管电泳(ace)分析方法，对表皮生长因子受体(EGFR)和新多肽配体GE11之间的结合能力进行分析。
The NGR peptide is a ligand specifically binding to tumor angiogenic blood vessels, and thus has potential usage in the diagnosis and therapy of tumor.
天门冬酰胺酰甘氨酰精氨酸(NGR)是特异性地定位于肿瘤新生血管受体的多肽基序，在肿瘤诊断和治疗方面具有潜在的应用前景。
RESULTS Short peptide displayed on phage specifically was bound to 2F2 and the binding was inhibited by natural JEV Ag.
结果筛选到的噬菌体能特异地与2F2结合，并且这种结合可被天然抗原所抑制。
The receptor-binding properties of insulin and its analogs with modified C-terminal peptide sequence of the B-chain have been studied in liver cells and fat cells.
研究了一些胰岛素B链羧端肽段改变了的类似物与肝细胞及脂肪细胞的受体蛋白结合性质。
The protein vehicle is characterized by a membrane-targeting peptide and a trans-membrane segment separated by a cytoplasmic amino acid sequence that includes a cytoplasmic affinity-binding domain.
所述蛋白运载体的特征是被包含细胞质亲和结合结构域的细胞质氨基酸序列分隔的膜靶向肽和跨膜区段。
AIM: To select the peptide binding to human transferring receptor (hTfR) from phage display 12 peptides library.
目的：从噬菌体呈现1 2肽库中筛选与人转铁蛋白受体结合的肽。
In addition, a group of small peptide with the binding activity of human heparanase small subunit is further obtained.
另外，还得到了一组具有人乙酰肝素酶小亚基结合活性的小肽。
The mechanism of macrolide's action indicates that the binding sites of macrolides are located inside the nascent peptide exit tunnel of the ribosomal 50S subunit near the peptidyl transferase center.
抗菌机制研究表明：大环内酯抗生素的作用靶点位于50S亚基肽通道的出口处，紧邻肽酰转移酶中心。
The present invention relates to 1,4-benzodiazepines or 1,4-benzothiazepines derivatized with a peptide that can inhibit the interaction between annexin and annexin binding proteins.
本发明涉及可以抑制膜联蛋白和膜联蛋白结合蛋白之间的相互作用的衍生有肽的1，4-苯并二氮杂?类或1，4-苯并硫杂吖庚因类。
Research about crystal structure of HLA-B27-peptide complexes suggested the specificity and plasticity of peptide-binding and subtypes dependent binding features.
对B27与抗原肽复合物晶体结构的研究表明，B27与抗原肽结合具有特异性和可塑性，不同亚型具有不同的结合特点。
Furthermore, the fluorescence spectroscopic results show that the peptide consisting of multi-copies of 11-amino acid can stabilize the structure of LDH through synergy and multi-sites binding.
进一步通过荧光光谱法证实，含多拷贝11 -氨基酸基序的多肽可通过多位点协同结合模式，稳定LDH酶的结构。
Furthermore, the fluorescence spectroscopic results show that the peptide consisting of multi-copies of 11-amino acid can stabilize the structure of LDH through synergy and multi-sites binding.
进一步通过荧光光谱法证实，含多拷贝11 -氨基酸基序的多肽可通过多位点协同结合模式，稳定LDH酶的结构。
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