4.7 Article

Preparation of macromolecular complexes for cryo-electron microscopy

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NATURE PROTOCOLS
卷 2, 期 12, 页码 3239-3246

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NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2007.452

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资金

  1. NATIONAL CENTER FOR RESEARCH RESOURCES [P41RR001219] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM029169, R01GM055440, R37GM029169] Funding Source: NIH RePORTER
  3. NCRR NIH HHS [P41 RR001219, P41 RR01219, P41 RR001219-25] Funding Source: Medline
  4. NIGMS NIH HHS [R01 GM55440, R37 GM029169, R01 GM029169-28, R01 GM055440-12, R01 GM055440, R37 GM29169, R01 GM029169] Funding Source: Medline

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This protocol describes the preparation of frozen-hydrated single-particle specimens of macromolecular complexes. First, it describes how to create a grid surface coated with holey carbon by first inducing holes in a Formvar film to act as a template for the holey carbon that is stable under cryo-electron microscopy (cryo-EM) conditions and is sample-friendly. The protocol then describes the steps required to deposit the homogeneous sample on the grid and to plunge-freeze the grid into liquid ethane at the temperature of liquid nitrogen, so that it is suitable for cryo-EM visualization. It takes 4-5 h to make several hundred holey carbon grids and about 1 h to make the frozen-hydrated grids. The time required for sample purification varies from hours to days, depending on the sample and the specific procedure required. A companion protocol details how to collect cryo-EM data using an FEI Tecnai transmission electron microscope that can subsequently be processed to obtain a three-dimensional reconstruction of the macromolecular complex.

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