Zafiu C, Hussain Z, Küpcü S, Masutani A, Kilickiran P, Sinner E-K
Laboratory for Synthetic Bio-architectures, Department of Nanobiotechnology, University of Natural Resources and Life Sciences, Vienna, Muthgasse 11, 1190 Vienna, Austria; Institute of Complex Systems, Structural Biochemistry (ICS-6), Forschungszentrum Jülich, 52425 Jülich, Germany.
School of Chemical and Materials Engineering (SCME), National University of Sciences & Technology (NUST), Sector H-12, 44000 Islamabad, Pakistan.
Biosens Bioelectron. 2016 Jun 15;80:161-170. doi: 10.1016/j.bios.2016.01.017. Epub 2016 Jan 7.
Interactions of bacteria with target molecules (e.g. antibiotics) or other microorganisms are of growing interest. The first barrier for targeting gram-negative bacteria is layer of a Lipopolysaccharides (LPS). Liquid crystal (LC) based sensors covered with LPS monolayers, as presented in this study, offer a simple model to study and make use of this type of interface for detection and screening. This work describes in detail the production and application of such sensors based on three different LPS that have been investigated regarding their potential to serve as sensing layer to detect bacteria. The LPS O127:B8 in combination with a LC based sensor was identified to be most useful as biomimetic sensing surface. This LPS/LC combination interacts with three different bacteria species, one gram-positive and two gram-negative species, allowing the detection of bacterial presence regardless from their viability. It could be shown that even very low bacterial cell numbers (minimum 500 cell ml(-1)) could be detected within minutes (maximum 15 min). The readout mechanism is the adsorption of bacterial entities on surface bond LPS molecules with the LC serving as an optical amplifier.
细菌与靶分子(如抗生素)或其他微生物之间的相互作用越来越受到关注。靶向革兰氏阴性菌的第一道屏障是一层脂多糖(LPS)。如本研究中所述,覆盖有LPS单层的基于液晶(LC)的传感器提供了一个简单的模型,用于研究和利用这种类型的界面进行检测和筛选。这项工作详细描述了基于三种不同LPS的此类传感器的制备和应用,这些LPS已被研究用作检测细菌的传感层的潜力。已确定LPS O127:B8与基于LC的传感器结合作为仿生传感表面最为有用。这种LPS/LC组合与三种不同的细菌物种相互作用,一种革兰氏阳性菌和两种革兰氏阴性菌,无论细菌的生存能力如何,都能检测到细菌的存在。结果表明,即使是非常低的细菌细胞数(最低500个细胞/毫升)也能在几分钟内(最长15分钟)被检测到。读出机制是细菌实体吸附在表面结合的LPS分子上,而LC用作光学放大器。