Institut für Röntgenphysik, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany.
Proc Natl Acad Sci U S A. 2010 Jan 12;107(2):529-34. doi: 10.1073/pnas.0905846107. Epub 2009 Dec 17.
Recent advances in coherent x-ray diffractive imaging have paved the way to reliable and quantitative imaging of noncompact specimens at the nanometer scale. Introduced a year ago, an advanced implementation of ptychographic coherent diffractive imaging has removed much of the previous limitations regarding sample preparation and illumination conditions. Here, we apply this recent approach toward structure determination at the nanoscale to biological microscopy. We show that the projected electron density of unstained and unsliced freeze-dried cells of the bacterium Deinococcus radiodurans can be derived from the reconstructed phase in a straightforward and reproducible way, with quantified and small errors. Thus, the approach may contribute in the future to the understanding of the highly disputed nucleoid structure of bacterial cells. In the present study, the estimated resolution for the cells was 85 nm (half-period length), whereas 50-nm resolution was demonstrated for lithographic test structures. With respect to the diameter of the pinhole used to illuminate the samples, a superresolution of about 15 was achieved for the cells and 30 for the test structures, respectively. These values should be assessed in view of the low dose applied on the order of approximately 1.3x10(5) Gy, and were shown to scale with photon fluence.
近年来,相干 X 射线衍射成象技术取得了突破性进展,为在纳米尺度对非致密样品进行可靠和定量成像铺平了道路。一年前推出的一种先进的相衬相干衍射成象实现方法,消除了以前在样品制备和照明条件方面的许多限制。在此,我们将这种最近的方法应用于纳米尺度的生物显微镜结构测定。我们表明,通过重建相位,可以以直接和可重复的方式,以量化的小误差,从未染色和未切片的冻干细菌 Deinococcus radiodurans 的细胞中得出其投射电子密度。因此,该方法可能有助于未来理解备受争议的细菌细胞拟核结构。在本研究中,对细胞的估计分辨率为 85nm(半周期长度),而对于光刻测试结构则证明了 50nm 的分辨率。对于所使用的照射样品的针孔直径,对于细胞分别实现了约 15 的超分辨率,对于测试结构则实现了 30 的超分辨率。这些值应考虑到应用的低剂量(约 1.3x10(5)Gy)进行评估,并表明与光子通量成比例。