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使用原子力显微镜绘制活微生物细胞的细胞壁多糖图谱。

Mapping cell wall polysaccharides of living microbial cells using atomic force microscopy.

作者信息

Gad M, Itoh A, Ikai A

机构信息

Biodynamics Laboratory, Tokyo Institute of Technology, Japan.

出版信息

Cell Biol Int. 1997 Nov;21(11):697-706. doi: 10.1006/cbir.1997.0214.

Abstract

Functionalized atomic force microscope tips were used to sense specific forces of interaction between ligand-receptor pairs and to map the positions of polysaccharides on a living microbial cell surface. Gold-coated tips were functionalized with concanavalin A using a cross-linker with a spacer arm of 15.6 A. It was possible to measure the binding force between concanavalin A and mannan polymers on the yeast (Saccharomyces cerevisiae) cell surface. This force ranged from 75 to 200 pN. The shape of the force curve indicated that the polymers were pulled away from the cell surface for a fairly long distance that sometimes reached several hundred nanometres. The distribution of mannan on the cell surface was mapped by carrying out the force measurement in the force volume mode of atomic force microscopy (AFM). During the measurement, the maximum cantilever deflection after contact between the tip and the sample was kept constant at 10 nm using trigger mode to keep the pressing force on the sample surface as gently as possible at a force of 180 pN. This regime was used to minimize the non-specific adhesion between the tip and the cell surface. Specific molecular recognition events took place on specific areas of the cell surface that could be interpreted as reflecting a non-uniform distribution of mannan on the cell surface.

摘要

功能化原子力显微镜探针用于感知配体 - 受体对之间的特定相互作用力,并绘制多糖在活微生物细胞表面的位置。使用具有15.6 Å间隔臂的交联剂,用伴刀豆球蛋白A对金涂层探针进行功能化。可以测量伴刀豆球蛋白A与酵母(酿酒酵母)细胞表面甘露聚糖聚合物之间的结合力。该力范围为75至200 pN。力曲线的形状表明,聚合物从细胞表面被拉开了相当长的距离,有时达到几百纳米。通过在原子力显微镜(AFM)的力体积模式下进行力测量,绘制了甘露聚糖在细胞表面的分布。在测量过程中,使用触发模式将探针与样品接触后的最大悬臂偏转保持在10 nm恒定,以在180 pN的力下尽可能轻柔地保持对样品表面的按压力。此模式用于最小化探针与细胞表面之间的非特异性粘附。特定的分子识别事件发生在细胞表面的特定区域,这可以解释为反映了甘露聚糖在细胞表面的不均匀分布。

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