Jonkman James, Brown Claire M, Cole Richard W
Advanced Optical Microscopy Facility (AOMF), University Health Network, Toronto, Ontario, Canada.
McGill University, Life Sciences Complex Advanced BioImaging Facility (ABIF), Montreal, Québec, Canada.
Methods Cell Biol. 2014;123:113-34. doi: 10.1016/B978-0-12-420138-5.00007-0.
Quantitative optical microscopy has become the norm, with the confocal laser-scanning microscope being the workhorse of many imaging laboratories. Generating quantitative data requires a greater emphasis on the accurate operation of the microscope itself, along with proper experimental design and adequate controls. The microscope, which is more accurately an imaging system, cannot be treated as a "black box" with the collected data viewed as infallible. There needs to be regularly scheduled performance testing that will ensure that quality data are being generated. This regular testing also allows for the tracking of metrics that can point to issues before they result in instrument malfunction and downtime. In turn, images must be collected in a manner that is quantitative with maximal signal to noise (which can be difficult depending on the application) without data clipping. Images must then be processed to correct for background intensities, fluorophore cross talk, and uneven field illumination. With advanced techniques such as spectral imaging, Förster resonance energy transfer, and fluorescence-lifetime imaging microscopy, experimental design needs to be carefully planned out and include all appropriate controls. Quantitative confocal imaging in all of these contexts and more will be explored within the chapter.
定量光学显微镜已成为常态,共聚焦激光扫描显微镜是许多成像实验室的主力设备。生成定量数据需要更加强调显微镜本身的准确操作,以及适当的实验设计和充分的对照。显微镜,更准确地说是一个成像系统,不能被视为一个“黑匣子”,而将收集到的数据视为绝对可靠。需要定期进行性能测试,以确保生成高质量的数据。这种定期测试还允许跟踪一些指标,这些指标可以在问题导致仪器故障和停机之前指出问题。反过来,必须以定量的方式收集图像,具有最大的信噪比(这可能因应用而异),且不进行数据裁剪。然后必须对图像进行处理,以校正背景强度、荧光团串扰和不均匀的场照明。对于光谱成像、Förster共振能量转移和荧光寿命成像显微镜等先进技术,实验设计需要精心规划,并包括所有适当的对照。本章将探讨所有这些情况下以及更多情况下的定量共聚焦成像。