Step-by-step guide to building an inexpensive 3D printed motorized positioning stage for automated high-content screening microscopy

被引:24
作者
Schneidereit, Dominik [1 ,2 ]
Kraus, Larissa [1 ,4 ,5 ]
Meier, Jochen C. [3 ]
Friedrich, Oliver [1 ,2 ]
Gilbert, Daniel F. [1 ,2 ]
机构
[1] Friedrich Alexander Univ Erlangen Nurnberg, Inst Med Biotechnol, Erlangen, Germany
[2] Friedrich Alexander Univ Erlangen Nurnberg, Erlangen Grad Sch Adv Opt Technol SAOT, Erlangen, Germany
[3] Tech Univ Carolo Wilhelmina Braunschweig, Inst Zool, Cell Physiol, Braunschweig, Germany
[4] Charite, Dept Neurol Clin & Expt Epileptol, Berlin, Germany
[5] Berlin Inst Hlth, Berlin, Germany
关键词
3D desktop printing; Arduino; High-content screening; Cell viability; YFPI152L; Glycine receptor; TRPV1; Fluo-4; AM; INHIBITORY GLYCINE RECEPTOR; LOW-COST; HIGH-THROUGHPUT; GABA(A) RECEPTOR; CHLORIDE CHANNEL; IDENTIFICATION; EXPRESSION; DISORDERS; MODULATOR; SUBUNIT;
D O I
10.1016/j.bios.2016.10.078
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
High-content screening microscopy relies on automation infrastructure that is typically proprietary, non customizable, costly and requires a high level of skill to use and maintain. The increasing availability of rapid prototyping technology makes it possible to quickly engineer alternatives to conventional automation infrastructure that are low-cost and user-friendly. Here, we describe a 3D printed inexpensive open source and scalable motorized positioning stage for automated high-content screening microscopy and provide detailed step-by-step instructions to re-building the device, including a comprehensive parts list, 3D design files in STEP (Standard for the Exchange of Product model data) and STL (Standard Tessellation Language) format, electronic circuits and wiring diagrams as well as software code. System assembly including 3D printing requires approx. 30 h. The fully assembled device is light-weight (1.1 kg), small (33x20x8 cm) and extremely low-cost (approx. EUR 250). We describe positioning characteristics of the stage, including spatial resolution, accuracy and repeatability, compare imaging data generated with our device to data obtained using a commercially available microplate reader, demonstrate its suitability to high-content microscopy in 96-well high-throughput screening format and validate its applicability to automated functional Cl- - and Ca2+-imaging with recombinant HEK293 cells as a model system. A time-lapse video of the stage during operation and as part of a custom assembled screening robot can be found at https://vimeo.com/158813199.
引用
收藏
页码:472 / 481
页数:10
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