Phasing electron diffraction data by molecular replacement: strategy for structure determination and refinement.

نویسندگان

  • Goragot Wisedchaisri
  • Tamir Gonen
چکیده

Electron crystallography is arguably the only electron cryomicroscopy (cryo EM) technique able to deliver atomic resolution data (better then 3 Å) for membrane proteins embedded in a membrane. The progress in hardware improvements and sample preparation for diffraction analysis resulted in a number of recent examples where increasingly higher resolutions were achieved. Other chapters in this book detail the improvements in hardware and delve into the intricate art of sample preparation for microscopy and electron diffraction data collection and processing. In this chapter, we describe in detail the protocols for molecular replacement for electron diffraction studies. The use of a search model for phasing electron diffraction data essentially eliminates the need of acquiring image data rendering it immune to aberrations from drift and charging effects that effectively lower the attainable resolution.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ab initio molecular-replacement phasing for symmetric helical membrane proteins

Obtaining phases for X-ray diffraction data can be a rate-limiting step in structure determination. Taking advantage of constraints specific to membrane proteins, an ab initio molecular-replacement method has been developed for phasing X-ray diffraction data for symmetric helical membrane proteins without prior knowledge of their structure or heavy-atom derivatives. The described method is base...

متن کامل

A Description of the Techniques and Application of Molecular Replacement Used to Determine the Structure of Polyoma Virus Capsid at 22.5 Å Resolution.

The electron density map of polyoma virus capsid crystals solved at 22.5 Å resolution by molecular replacement [Rayment, Baker, Caspar & Murakami (1982). Nature (London), 295, 110-115] shows that the 72 capsomeres that form the polyoma capsid are all pentamers. An extensive series of refinement calculations were undertaken to demonstrate the validity of this unexpected result. This report descr...

متن کامل

Macromolecular Crystallography for Synthetic Abiological Molecules: Combining xMDFF and PHENIX for Structure Determination of Cyanostar Macrocycles.

Crystal structure determination has long provided insight into structure and bonding of small molecules. When those same small molecules are designed to come together in multimolecular assemblies, such as in coordination cages, supramolecular architectures and organic-based frameworks, their crystallographic characteristics closely resemble biological macromolecules. This resemblance suggests t...

متن کامل

Determination and Refinement of the AgySis111d-s3 3 1d Surface Structure

A new model for the AgySis111d-s3 3 1d surface is proposed based on direct phasing of transmission electron diffraction data. The atomic positions in the model are refined using dynamical diffraction calculations. Other existing models were simulated and could not fit the diffraction pattern. The new model is consistent with the experimental results reported in the literature on this surface. [...

متن کامل

Recent developments in phasing and structure refinement for macromolecular crystallography.

Central to crystallographic structure solution is obtaining accurate phases in order to build a molecular model, ultimately followed by refinement of that model to optimize its fit to the experimental diffraction data and prior chemical knowledge. Recent advances in phasing and model refinement and validation algorithms make it possible to arrive at better electron density maps and more accurat...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Methods in molecular biology

دوره 955  شماره 

صفحات  -

تاریخ انتشار 2013