小组主要研究了将类似表面活性剂的短链多肽结合到脂类纳米结构之后对后者的影响。
They detailed their findings in the report on the impact of integrating short surfactant-like designer peptides in lipidic nanostructures.
与此同时，由于放置于表面的多肽类蛋白质碎片，聚丙烯延胡索酸酯与身体结合。
While this happens, the polypropylene fumarate becomes integrated with the body thanks to protein fragments called peptides placed on its surface.
20种不同的有机分子结合起来组成多肽链或蛋白质。这20个氨基酸主结构相同，但每种又分别有各自不同的侧基团。
One of the 20 different organic molecules that are joined together to form a polypeptide chain or a protein the twenty amino acids share a common backbone, but each has a specific side-group.
基本的单链多肽，通过与酶的活性位点紧密结合形成复合物，抑制大多数的丝氨酸蛋白酶。
Basic single-chain polypeptide that inhibits numerous serine proteases by binding to the active site of the enzyme, forming tight complexes.
CBLB502是一种多肽药物，它来源于沙门氏菌鞭毛蛋白的一部分，结合并有效地激活tlr5。
CBLB502 is a polypeptide drug derived from a portion of Salmonella flagellin that binds to and potently activates TLR5.
多年来，人们常假定孵育后的细胞再用缓冲液洗涤时，能导致细胞膜结合多肽的解吸附作用。
Over the years, it has frequently been assumed that washing the cells with buffer after incubation causes desorption of peptide associated with the plasma membrane.
甲状旁腺激素相关蛋白是与甲状旁腺激素同源的一种多肽类物质，二者结合于同一种细胞膜受体。
Parathyroid hormone-related protein (PTI-IrP) is a homogenous peptide of parathyroid hormone, and both of them bind to the same membrane receptor.
目的寻找与人巨细胞病毒（HCMV）PPUL44蛋白核定位信号（NLS）具有较强结合能力的多肽，研究这些多肽的氨基酸序列特点。
Objective To find the peptides that have strong binding ability to the nuclear localization signals (NLS) of human Cytomegalovirus (HCMV) PPUL44 protein, and to analyze their amino acid sequences.
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 binding ability of new peptide ligand GE11 and epidermal growth factor receptor (EGFR) was analyzed by affinity capillary electrophoresis (ACE) method.
大量定点突变实验、选择性化学修饰实验、抗多肽抗体结合实验等能很好地确证该联配结果的正确性。
The reliability of the method was confirmed by site-directed mutagenesis, selective chemical modification, site-specific antipeptide antibody binding experiments, and so on.
在研究中，结合多肽的药物和光线可以杀死1000万葡萄球菌细胞的99.97%。
In the study, the combination of the drug, the peptides and the light killed 99.97 percent of 10 million MRSA cells.
病毒颗粒可以包裹一种多肽，能够和整合素特异性结合。
The virus particles could be coated externally with peptides that bind to integrins.
该单克隆抗体用磷酸化丝氨酸14-3-3结合基序多肽免疫动物制备。
Monoclonal antibody is produced by immunizing animals with phospho-(Ser) 14-3-3 binding motif peptides .
从以色列蝎子中提取出多肽物氯毒素是特异性离子通道阻滞剂，能特异性与胶质瘤细胞表面的氯离子通道结合，进而杀死肿瘤细胞。
Catilan extracted from Leiurus quinquestriatus is a specific ion channel blocker. It can specifically bind chloride channels of glioma cells and kill these tumor cells.
对结合多肽序列的预测可以大大减少实验所需的费用和时间。
Prediction methods for identifying binding peptides could minimize the number of peptides required to be synthesized and assayed, therefore reduce laboratory time and costs.
本发明涉及重组多肽，特别是结合纤连蛋白的Ed-B-同种型并可阻断其功能的抗体或抗体片段。
The invention relates to recombinant polypeptides, in particular antibodies or antibody fragments, which are able to bind the ED-B isoform of fibronectin and block the function thereof.
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。
Objective To investigate the effect of resistin and resistin binding peptide(RBP) on the glucose uptake in L6 rat skeletal muscle cells.
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.
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。
This study utilized purified IBV H52 strain to screen specific virus-binding peptides from Ph. D. -12TM phage display peptide library.
观察重组人纤维结合素多肽CH5 0对化疗小鼠巨噬细胞的影响。
The influence of CH50, a recombinant polypeptide of human fibronectin, on the function of macrophages of mice during chemotherapy was observed.
从骨组织Sialoprotein 中衍生的可与骨胶原结合的多肽药物，具促进骨组织修补和再生的功能。
A suite of proprietary collagen-binding peptides derived from bone sialoprotein (BSP) that are effective in promoting bone repair and regeneration.
从骨组织Sialoprotein 中衍生的可与骨胶原结合的多肽药物，具促进骨组织修补和再生的功能。
A suite of proprietary collagen-binding peptides derived from bone sialoprotein (BSP) that are effective in promoting bone repair and regeneration.
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