近场扫描光学成像结合量子点标记的纳米技术在细胞生物学中的应用

近场扫描光学显微镜（NSOM）对传统的光学分辨极限产生了革命性的突破,可在超高光学分辨率下无侵人性和无破坏性地对生物样品进行观测。量子点（QDs）具有极好的光学性能,如荧光寿命长、激发谱宽、生物相容性强、光稳定性好等优点,适合先进的生物成像。NSOM结合QDs标记的纳米技术被应用在细胞生物学中。通过纳米量级NSOM免疫荧光成像（50nm）对特定蛋白分子在细胞表面的动态分布进行可视化研究和数量化分析,阐明了蛋白分子在不同细胞过程中的作用机制。因此,NSOM／QD基成像系统提供了单个蛋白分子最高分辨率的荧光图像,为可视化研究蛋白分子机制的提供了一种强有力的工具。     

生物技术发展趋势与预测

预测了未来10～20年内生物技术在人类医学领域、农业生物技术领域、工业生物技术领域、生物计算学领域、材料学领域、生物工程领域和环境生物工程领域的主要发展趋势,对生物技术的发展进程也作了预测,并对生物技术在人类疾病治疗方面、农业领域、工业领域、数学领域、材料学科、生物工程方面和环境生物工程领域作出了实际预测。     

北京生物技术产业发展研究

生物技术及其相关产业是北京重点发展的高新技术领域之一.“九五”以来北京在该领域取得了稳步发展,具有研发、人才和临床优势.概述了近年来北京生物技术领域在研究、产业、政策等领域的发展现状,提出了目前北京在该领域发展面临的主要问题,并以此为基础为北京市该领域未来发展提出了相关建议.     

2022年再生医学领域发展态势

再生医学领域经过多年的发展,在多种疾病治疗中展现出巨大应用潜力。近年来,大数据、学科融合等研究理念的不断渗透,以及一系列通用技术在再生医学领域的广泛应用,推动再生医学研究广度和深度持续拓展,领域范畴也不断拓宽,为该领域带来了全新的发展机遇。本文从科技规划、监管政策、科技及产业进展等角度,对再生医学热点领域2022年的发展趋势进行了分析,并对相关领域未来的发展进行了展望。     

生命起源RNA世界的提出者——奥吉尔

奥吉尔是一位伟大的科学家,在化学领域提出了配位场理论,在生命起源领域提出了RNA世界假说,尤其在生命起源领域的研究为推动人们对早期生命诞生有了新的理解,撰写此文能够使大家对该科学家有一个较为全面的了解。     

更正启事

为促进中法两国在生物制药和生物孵化器等领域的合作与交流,2006年5月23日在北京兆龙饭店举行了中法生物医药论坛。与会代表100余名,他们来自生物医药领域的企业、研究机构、风险投资公司、政策研究等单位。在相互了解两国生物医药领域的现状后,共同探讨了该领域的发展趋势,以及如何通过合作促进双方发展等问题。     

酪氨酸酶的应用研究进展

酪氨酸酶具有重要的生理生化特性,在医药、环境、食品、精细化工等领域具有广泛的用 途。酪氨酸酶可以氧化L-酪氨酸合成L-多巴和黑色素,L-多巴用于帕金森症的治疗,黑色素能够 杀死HIV病毒。酪氨酸酶可用于环境工程领域处理含苯酚及胺类废水,用于精细化工领域催化 有机合成反应。综述了酪氨酸酶在各个领域的应用概况,阐明了其在工业生产领域的应用前景。     

合成生物学领域专利竞争态势分析

合成生物学是生物学、工程学、化学和信息技术等相互交叉融合的一个新兴领域,在医学、药物、农业、材料、环境和能源等领域具有广阔的应用前景,甚至可能创造出自然界中没有的新生物,被视为生物科技领域的颠覆性技术。分析了合成生物学领域主要国家和地区的相关发展战略、资助项目和政策措施,总结了合成生物学领域专利技术的发展历程,揭示了该领域的专利研发主题分布情况,综合对比分析了该领域的主要国家和主要机构的专利产出情况,以期为我国合成生物学领域的科研工作者和管理决策者提供参考数据。     

纳米材料在农作物领域的应用及展望

近年来,纳米材料成为农业领域的一个研究热点,受到了国内外学者的广泛关注。纳米材料基于其尺寸小的特点,可以在穿透植物细胞壁后,通过内吞作用被细胞吸收,进而对植物生长产生影响。纳米材料被广泛应用于植物遗传转化、作物生长发育和植物健康等农作物领域,尤其在遗传转化领域,其可作为转化载体与基因编辑技术综合运用,对作物进行遗传改良。基于此,对纳米材料在植物体内的吸收、转运机制及其在农作物领域的应用进展进行了综述,重点探讨了纳米材料在植物遗传转化方面的研究进展,并对其在农作物领域亟待解决的问题和后续发展方向进行了展望,以期为拓宽纳米材料的应用领域提供参考。     

酵母双杂交在植物功能基因组研究中的应用

扼要介绍了酵母双杂交技术的原理,详细评述了该技术在植物功能基因组中的研究进展,并结合自己研究领域对该技术在植物领域发展方向作了展望。     

Scanning near-field fluorescence resonance energy transfer microscopy

A new microscopic technique is demonstrated that combines attributes from both near-field scanning optical microscopy (NSOM) and fluorescence resonance energy transfer (FRET). The method relies on attaching the acceptor dye of a FRET pair to the end of a near-field fiber optic probe. Light exiting the NSOM probe, which is nonresonant with the acceptor dye, excites the donor dye introduced into a sample. As the tip approaches the sample containing the donor dye, energy transfer from the excited donor to the tip-bound acceptor produces a red-shifted fluorescence. By monitoring this red-shifted acceptor emission, a dramatic reduction in the sample volume probed by the uncoated NSOM tip is observed. This technique is demonstrated by imaging the fluorescence from a multilayer film created using the Langmuir-Blodgett (LB) technique. The film consists of L-alpha-dipalmitoylphosphatidylcholine (DPPC) monolayers containing the donor dye, fluorescein, separated by a spacer group of three arachidic acid layers. A DPPC monolayer containing the acceptor dye, rhodamine, was also transferred onto an NSOM tip using the LB technique. Using this modified probe, fluorescence images of the multilayer film reveal distinct differences between images collected monitoring either the donor or acceptor emission. The latter results from energy transfer from the sample to the NSOM probe. This method is shown to provide enhanced depth sensitivity in fluorescence measurements, which may be particularly informative in studies on thick specimens such as cells. The technique also provides a mechanism for obtaining high spatial resolution without the need for a metal coating around the NSOM probe and should work equally well with nonwaveguide probes such as atomic force microscopy tips. This may lead to dramatically improved spatial resolution in fluorescence imaging.     

Near-Field Scanning Optical Microscopy, a Siren Call to Biology

Near-field illumination of a sample with visible light can resolve features well beyond the resolution of conventional, far-field microscopes. Near-field scanning optical microscopy (NSOM) then has the potential of extending the resolution of techniques such as fluorescent labeling, yielding images of cell structures and molecules on the nanoscale. However, major problems remain to be solved before NSOM can be easily used for wet biological samples. The most significant of these is control of the distance between near-field aperture and the sample surface. Hence, while NSOM promises much, its application to biology is about where electron microscopy was 40 or 50 years ago.     

Submicron structure in L-alpha-dipalmitoylphosphatidylcholine monolayers and bilayers probed with confocal, atomic force, and near-field microscopy.

Langmuir-Blodgett (LB) monolayers and bilayers of L-alpha-dipalmitoylphosphatidylcholine (DPPC), fluorescently doped with 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (diIC18), are studied by confocal microscopy, atomic force microscopy (AFM), and near-field scanning optical microscopy (NSOM). Beyond the resolution limit of confocal microscopy, both AFM and NSOM measurements of mica-supported lipid monolayers reveal small domains on the submicron scale. In the NSOM studies, simultaneous high-resolution fluorescence and topography measurements of these structures confirm that they arise from coexisting liquid condensed (LC) and liquid expanded (LE) lipid phases, and not defects in the monolayer. AFM studies of bilayers formed by a combination of LB dipping and Langmuir-Schaefer monolayer transfer exhibit complex surface topographies that reflect a convolution of the phase structure present in each of the individual monolayers. NSOM fluorescence measurements, however, are able to resolve the underlying lipid domains from each side of the bilayer and show that they are qualitatively similar to those observed in the monolayers. The observation of the small lipid domains in these bilayers is beyond the spatial resolving power of confocal microscopy and is complicated in the topography measurements taken with AFM, illustrating the utility of NSOM for these types of studies. The data suggest that the small LC and LE lipid domains are formed after lipid transfer to the substrate through a dewetting mechanism. The possible extension of these measurements to probing for lipid phase domains in natural biomembranes is discussed.     

Near-field scanning fluorescence microscopy study of ion channel clusters in cardiac myocyte membranes

Near-field scanning optical microscopy (NSOM) has been used to study the nanoscale distribution of voltage-gated L-type Ca²⁺ ion channels, which play an important role in cardiac function. NSOM fluorescence imaging of immunostained cardiac myocytes (H9C2 cells) demonstrates that the ion channel is localized in small clusters with an average diameter of 100 nm. The clusters are randomly distributed throughout the cell membrane, with some larger fluorescent patches that high-resolution images show to consist of many small closely-spaced clusters. We have imaged unstained cells to assess the contribution of topography-induced artifacts and find that the topography-induced signal is <10% of the NSOM fluorescence intensity. We have also examined the dependence of the NSOM signal intensity on the tip-sample separation to assess the contributions from fluorophores that are significantly below the cell surface. This indicates that chromophores >~200 nm below the probe will have negligible contributions to the observed signal. The ability to quantitatively measure small clusters of ion channels will facilitate future studies that examine changes in protein localization in stimulated cells and during cardiac development. Our work illustrates the potential of NSOM for studying membrane domains and protein localization/colocalization on a length scale which exceeds that available with optical microscopy.     

Application of near-field scanning optical microscopy in photosynthesis research

Many different methods have been developed in recent years to gain insight into the structure of proteins, membranes, organelles and cells. Here we demonstrate the application of near-field scanning optical microscopy (NSOM) for analysis of the structures of typical photosynthetic membrane objects such as chloroplasts and thylakoids from spinach and chromatophores from purple bacteria. To our knowledge, this is the first report of application of NSOM to imaging chromatophores from photosynthetic bacteria and intact thylakoids from higher plants. NSOM has the ability to measure optical signals originating from the sample with a spatial resolution better than conventional optical microscopy. The main advantage of near-field optical microscopy, besides the improved lateral optical resolution, is the simultaneously acquired topography. We have applied NSOM to thylakoids obtained by osmotic shock of chloroplasts. Swollen thylakoids had average diameters of 0.8–1 micron and heights of 0.05–0.07 micron. We also describe the use of fluorescent dyes for the analysis of structures resulting from fusion of photosynthetic bacterial chromatophores with lipid impregnated collodion membranes. The structures formed after fusion of chromatophores to the collodion film have diameters ranging from 0.2 to 10 microns and heights from 0.01 to 1 micron. The dual functionality (optical and topographical), high spatial resolution, and the possibility to work with wet samples and under water, make NSOM a useful method for examining the structures, sizes, and heterogeneity of chromatophore and thylakoid preparations.     

Imaging of Oil/Monoglyceride Networks by Polarizing Near-Field Scanning Optical Microscopy

Polarizing near-field scanning optical microscopy (NSOM) was applied for visualization of lipid coagel structures. The technique ensures obtaining polarization contrast images at micro- and nanoscale resolution. Comparison to the polarizing light microscopy images revealed that the same fractal structural organization persists also at submicron scale, at the level of primary ordered structures creation. Many long birefringent needle-shaped primary crystallites were imaged in the corn oil:monoglyceride samples, and lower amount of smaller oval-shaped primary crystallites—in the olive oil:monoglyceride samples. Unlike atomic force microscopy, polarizing NSOM brought direct evidence on the physical state of specific features. Compared to the polarizing light microscopy, polarizing NSOM provided additional information on the structural organization of oil–monoglyceride coagels at the micro- and submicron scale.     

Near-field optical analysis of living cells in vitro

Near-field optical analysis (NOA) provides morphological nanoscale mappings of living cells in liquid cell culture media and nondestructive insight into cell functionality. Here we show for the first time the performance of NOA in imaging living cells. Unlabeled human endothelial cells attached to polished titanium disks were analyzed with hydrophobically coated optical biosensors mounted to a near-field scanning optical microscope (NSOM). Biosensors and titanium substrates could be simply implemented in standard NSOM and high-throughput NOA.     

The optical near-field and cell biology

A new form of scanning light microscopy is described in which the lens is replaced by a point of light that is smaller than the wavelength. Resolution is obtained that is defined not by the wavelength but by the size of the spot of light. This is the case so long as the point of light is within the dimension of a wavelength from the surface that is to imaged or within the optical near-field. This new form of light microscopy is called near-field scanning optical microscopy (NSOM). Resolutions are being obtained with NSOM that are similar to scanning electron microscopy but without the destructive effects of a vacuum or of an electron beam. In addition such a microscope is readily interfaced with fluorescent and non-fluorescent contrast enhancing stains that are commonly used in cell biology. The possibility of a near-field/far-field microscope is discussed with overlapping resolutions from a few hundred of a conventional microscope to the tens of thousand that can be obtained with NSOM.     

Study of the Plasmon Talbot Effect of Metallic Nanolenses Induced by Linearly Polarized Illumination

The plasmon Talbot effect of metallic nanolenses was studied theoretically and experimentally for the linearly polarized incident beam case. To demonstrate this self-imaging-based focusing property of the metallic nanolenses, a plasmonic nanolens with five periodic concentric through rings on Al film supported on quartz substrate was numerically studied firstly by the use of rigorous finite-difference and time-domain algorithm. To further demonstrate its working performance experimentally, it was fabricated by means of a focused ion beam direct milling technique. A near-field scanning optical microscope (NSOM) was then employed for the optical characterization of its focusing property. The experimental results indicate that the NSOM probing-based results are in agreement with the theoretical calculation results in general.