The use of amphipathic polymers for cryo electron microscopy of NADH:ubiquinone oxidoreductase (complex I).
نویسندگان
چکیده
In the three-dimensional (3D) structure determination of macromolecules, cryo electron microscopy (cryo-EM) is an important method for obtaining micrographs of unstained specimens for the single-particle reconstruction approach. For cryo-EM, proteins are fixed in a frozen hydrated state by quick-freezing in a thin water layer on a holey carbon film. Cryo-EM of detergent-solubilized membrane proteins is hindered by the fact that detergents reduce the surface tension of water, so that it is difficult to control the ice thickness and the distribution of protein. Amphipols are a new class of amphipathic polymers designed to handle membrane proteins in aqueous solutions under particularly mild conditions. Amphipol A8-35 stabilizes NADH:ubiquinone oxidoreductase (complex I) from Neurospora crassa and keeps it water-soluble in the absence of free detergent. Electron microscope images of quick-frozen complex I/A8-35 samples were used for computer-based single-particle averaging and 3D reconstruction, and the reconstruction of unstained frozen-hydrated particles compared with previous detergent-based reconstructions. The potential of amphipols for cryo-EM is discussed.
منابع مشابه
Structure of the respiratory NADH:ubiquinone oxidoreductase (complex I)
Three-dimensional structures of NADH:ubiquinone oxidoreductase (or complex I) from the respiratory chain of mitochondria and bacteria have been recently studied by electron microscopy. The low-resolution structures all reveal a characteristic L shape for complex I; however, some of the differences among these structures may have important implications for the location of the functional elements...
متن کاملNucleotide-induced conformational changes in the Escherichia coli NADH:ubiquinone oxidoreductase (complex I).
The energy-converting NADH:ubiquinone oxidoreductase, also known as respiratory complex I, couples the transfer of electrons from NADH to ubiquinone with the translocation of protons across the membrane. Electron microscopy revealed the two-part structure of the complex consisting of a peripheral and a membrane arm. The peripheral arm contains all known cofactors and the NADH-binding site, wher...
متن کاملThe Campylobacter jejuni NADH:ubiquinone oxidoreductase (complex I) utilizes flavodoxin rather than NADH.
Campylobacter jejuni encodes 12 of the 14 subunits that make up the respiratory enzyme NADH:ubiquinone oxidoreductase (also called complex I). The two nuo genes not present in C. jejuni encode the NADH dehydrogenase, and in their place in the operon are the novel genes designated Cj1575c and Cj1574c. A series of mutants was generated in which each of the 12 nuo genes (homologues to known comple...
متن کاملExternal alternative NADH:ubiquinone oxidoreductase redirected to the internal face of the mitochondrial inner membrane rescues complex I deficiency in Yarrowia lipolytica.
Alternative NADH:ubiquinone oxidoreductases are single subunit enzymes capable of transferring electrons from NADH to ubiquinone without contributing to the proton gradient across the respiratory membrane. The obligately aerobic yeast Yarrowia lipolytica has only one such enzyme, encoded by the NDH2 gene and located on the external face of the mitochondrial inner membrane. In sharp contrast to ...
متن کاملComplexes I in the Green Lineage
L. Sazanov (ed.), A Structural Perspective on Respiratory Complex I: Structure and Function of NADH:ubiquinone oxidoreductase, DOI 10.1007/978-94-007-4138-6_11, © Springer Science+Business Media Dordrecht 2012 Abstract In land plants and green algae, mitochondria and chloroplasts were acquired sequentially through primary endosymbiotic events with a a -proteobacterium and a cyanobacterium, resp...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of microscopy
دوره 227 Pt 3 شماره
صفحات -
تاریخ انتشار 2007