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Atomic force microscopy applications in macromolecular crystallography
Author(s) -
McPherson A.,
Malkin A. J.,
Kuznetsov Yu. G.,
Plomp M.
Publication year - 2001
Publication title -
acta crystallographica section d
Language(s) - English
Resource type - Journals
ISSN - 1399-0047
DOI - 10.1107/s0907444901008824
Subject(s) - nucleation , supersaturation , crystallization , atomic force microscopy , macromolecule , crystallography , protein crystallization , crystal growth , crystal (programming language) , resolution (logic) , materials science , chemical physics , diffraction , nucleic acid , exponential growth , nanotechnology , chemistry , optics , physics , computer science , biochemistry , programming language , organic chemistry , artificial intelligence , quantum mechanics
Atomic force microscopy (AFM) can be applied both in situ and ex situ to study the growth of crystals from solution. The method is particularly useful for investigating the crystallization of proteins, nucleic acids and viruses because it can be carried out in the mother liquor and in a non‐perturbing fashion. Interactions and transformations between various growth mechanisms can be directly visualized as a function of supersaturation, as can the incorporation of diverse impurities and the formation and propagation of defects. Because the crystals can be observed over long periods, it is also possible to obtain precise quantitative measures of the kinetic parameters for nucleation and growth. Finally, AFM has allowed us to identify a number of previously unsuspected phenomena that influence nucleation, rate of growth and the ultimate perfection of macromolecular crystals. These are all features which are important in determining the ultimate resolution and quality of a crystal's diffraction pattern.

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