The potential and limitations of neutrons, electrons and X-rays for atomic resolution microscopy of unstained biological molecules
- PMID: 7568675
- DOI: 10.1017/s003358350000305x
The potential and limitations of neutrons, electrons and X-rays for atomic resolution microscopy of unstained biological molecules
Abstract
Radiation damage is the main problem which prevents the determination of the structure of a single biological macromolecule at atomic resolution using any kind of microscopy. This is true whether neutrons, electrons or X-rays are used as the illumination. For neutrons, the cross-section for nuclear capture and the associated energy deposition and radiation damage could be reduced by using samples that are fully deuterated and 15N-labelled and by using fast neutrons, but single molecule biological microscopy is still not feasible. For naturally occurring biological material, electrons at present provide the most information for a given amount of radiation damage. Using phase contrast electron microscopy on biological molecules and macromolecular assemblies of approximately 10(5) molecular weight and above, there is in theory enough information present in the image to allow determination of the position and orientation of individual particles: the application of averaging methods can then be used to provide an atomic resolution structure. The images of approximately 10,000 particles are required. Below 10(5) molecular weight, some kind of crystal or other geometrically ordered aggregate is necessary to provide a sufficiently high combined molecular weight to allow for the alignment. In practice, the present quality of the best images still falls short of that attainable in theory and this means that a greater number of particles must be averaged and that the molecular weight limitation is somewhat larger than the predicted limit. For X-rays, the amount of damage per useful elastic scattering event is several hundred times greater than for electrons at all wavelengths and energies and therefore the requirements on specimen size and number of particles are correspondingly larger. Because of the lack of sufficiently bright neutron sources in the foreseeable future, electron microscopy in practice provides the greatest potential for immediate progress.
Similar articles
-
Biophysical methods: structure, function and dynamics studies of macromolecular assemblies using electrons, lasers, neutrons and X-rays.Curr Opin Struct Biol. 2008 Oct;18(5):577-80. doi: 10.1016/j.sbi.2008.09.001. Epub 2008 Sep 29. Curr Opin Struct Biol. 2008. PMID: 18801436 No abstract available.
-
Coherent and incoherent imaging of biological specimens with electrons and X-rays.Ultramicroscopy. 2021 Dec;231:113301. doi: 10.1016/j.ultramic.2021.113301. Epub 2021 May 6. Ultramicroscopy. 2021. PMID: 34006395
-
Holography and coherent diffraction with low-energy electrons: A route towards structural biology at the single molecule level.Ultramicroscopy. 2015 Dec;159 Pt 2:395-402. doi: 10.1016/j.ultramic.2014.11.024. Epub 2014 Dec 2. Ultramicroscopy. 2015. PMID: 25687733
-
Radiation damage in the high resolution electron microscopy of biological materials: a review.J Microsc. 1978 Jul;113(2):113-29. doi: 10.1111/j.1365-2818.1978.tb02454.x. J Microsc. 1978. PMID: 355638 Review.
-
Neutron microscopy. The low-damage imaging of specialized organic materials.Cell Biophys. 1985 Mar;7(1):1-29. doi: 10.1007/BF02788636. Cell Biophys. 1985. PMID: 2408753 Review.
Cited by
-
Design and characterization of modular scaffolds for tubulin assembly.J Biol Chem. 2012 Sep 7;287(37):31085-94. doi: 10.1074/jbc.M112.383869. Epub 2012 Jul 12. J Biol Chem. 2012. PMID: 22791712 Free PMC article.
-
Hydrogens and hydrogen-bond networks in macromolecular MicroED data.J Struct Biol X. 2022 Nov 10;6:100078. doi: 10.1016/j.yjsbx.2022.100078. eCollection 2022. J Struct Biol X. 2022. PMID: 36507068 Free PMC article.
-
Shake-up and shake-off excitations with associated electron losses in X-ray studies of proteins.Protein Sci. 2001 Dec;10(12):2480-4. doi: 10.1110/ps.ps.26201. Protein Sci. 2001. PMID: 11714915 Free PMC article.
-
Benchmarking the ideal sample thickness in cryo-EM.Proc Natl Acad Sci U S A. 2021 Dec 7;118(49):e2108884118. doi: 10.1073/pnas.2108884118. Proc Natl Acad Sci U S A. 2021. PMID: 34873060 Free PMC article.
-
Single particle electron microscopy.Photosynth Res. 2009 Nov-Dec;102(2-3):189-96. doi: 10.1007/s11120-009-9443-1. Photosynth Res. 2009. PMID: 19513809 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources