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PILATUS 1M探测器。

The PILATUS 1M detector.

作者信息

Broennimann Ch, Eikenberry E F, Henrich B, Horisberger R, Huelsen G, Pohl E, Schmitt B, Schulze-Briese C, Suzuki M, Tomizaki T, Toyokawa H, Wagner A

机构信息

Paul Scherrer Institute, CH-5232 Villigen, Switzerland.

出版信息

J Synchrotron Radiat. 2006 Mar;13(Pt 2):120-30. doi: 10.1107/S0909049505038665. Epub 2006 Feb 17.

Abstract

The PILATUS 1M detector is a hybrid pixel array detector with over one million pixels that operate in single photon counting mode. The detector, designed for macromolecular crystallography, is the largest pixel array detector currently in use at a synchrotron. It is a modular system consisting of 18 multichip modules covering an area of 21 cm x 24 cm. The design of the components as well as the manufacturing of the detector including the bump-bonding was performed at the Paul Scherrer Institute (PSI). The use of a single photon counting detector for protein crystallography requires detailed studies of the charge collection properties of the silicon sensor. The 18 modules are read out in parallel, leading to a full frame readout-time of 6.7 ms. This allows crystallographic data to be acquired in fine-varphi-slicing mode with continuous rotation of the sample. The detector was tested in several experiments at the protein crystallography beamline X06SA at the Swiss Light Source at PSI. Data were collected both in conventional oscillation mode using the shutter, as well as in a fine-varphi-slicing mode. After applying all the necessary corrections to data from a thaumatin crystal, the processing of the conventional data led to satisfactory merging R-factors of the order of 8.5%. This allows, for the first time, determination of a refined electron density map of a macromolecular biological crystal using a silicon pixel detector.

摘要

PILATUS 1M探测器是一种混合像素阵列探测器,拥有超过一百万个以单光子计数模式工作的像素。该探测器专为大分子晶体学设计,是目前同步加速器中使用的最大像素阵列探测器。它是一个模块化系统,由18个多芯片模块组成,覆盖面积为21厘米×24厘米。探测器的组件设计以及包括凸点键合在内的制造工作均在保罗·谢勒研究所(PSI)完成。将单光子计数探测器用于蛋白质晶体学需要对硅传感器的电荷收集特性进行详细研究。18个模块并行读出,全帧读出时间为6.7毫秒。这使得晶体学数据能够在样品连续旋转的精细φ切片模式下采集。该探测器在PSI瑞士光源的蛋白质晶体学光束线X06SA上进行了多次实验测试。数据采集既采用了使用快门的传统振荡模式,也采用了精细φ切片模式。对来自奇异果甜蛋白晶体的数据应用所有必要校正后,传统数据处理得到了约8.5%的令人满意的合并R因子。这首次使得使用硅像素探测器确定大分子生物晶体的精细电子密度图成为可能。

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