A repeating particle associated with the cristae and the inner membrane of the external envelope has been recognized and characterized in beef heart mitochondria by correlated electron microscopic and biochemical studies. Many thousands (ca. 104 to 105) of these particles, disposed in regular arrays, are present in a single mitochondrion. The repeating particle, called the elementary particle (EP), consists of three parts: (1) a spherical or polyhedral head piece (80 to 100 A in diameter); (2) a cylindrical stalk (about 50 A long and 30 to 40 A wide); and (3) a base piece (40 x 110 A). The base pieces of the elementary particles form an integral part of the outer dense layers of the cristae. The elementary particles can be seen in electron micrographs of mitochondria in situ, of isolated mitochondria, and of submitochondrial particles with a complete electron transfer chain. Negative staining with phosphotungstate is only one of several techniques that can be used for reproducible demonstration of the repeating particles and underlying subunit organization of mitochondrial membranes. A particulate unit containing a complete electron transfer chain can be isolated from beef heart mitochondria. The isolated unit approximates in size that of the elementary particle in situ. The molecular weight of the particle in situ is calculated to be 1.3 x 106. Evidence is presented for identifying the isolated unit with the elementary particle visualized in situ. The elementary particle of the mitochondrion is believed to be a prototype of a class of functional particles or macromolecular assemblies of similar size found in association with membranes generally.
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1 July 1964
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July 01 1964
A MACROMOLECULAR REPEATING UNIT OF MITOCHONDRIAL STRUCTURE AND FUNCTION : Correlated Electron Microscopic and Biochemical Studies of Isolated Mitochondria and Submitochondrial Particles of Beef Heart Muscle
H. Fernández-Morán,
H. Fernández-Morán
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
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T. Oda,
T. Oda
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
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P. V. Blair,
P. V. Blair
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
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D. E. Green
D. E. Green
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
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H. Fernández-Morán
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
T. Oda
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
P. V. Blair
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
D. E. Green
From the Mixter Laboratories for Electron Microscopy, Neurosurgical Service, Massachusetts General Hospital, Boston, and The Department of Biophysics, University of Chicago; and the Institute for Enzyme Research, University of Wisconsin, Madison.
Dr. Fernández-Morán's present address is Department of Biophysics, University of Chicago. Dr. Oda's present address is Department of Pathology, Okayama University Medical School, Okayama, Japan
Received:
November 01 1963
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1964 by The Rockefeller Institute Press
1964
J Cell Biol (1964) 22 (1): 63–100.
Article history
Received:
November 01 1963
Citation
H. Fernández-Morán, T. Oda, P. V. Blair, D. E. Green; A MACROMOLECULAR REPEATING UNIT OF MITOCHONDRIAL STRUCTURE AND FUNCTION : Correlated Electron Microscopic and Biochemical Studies of Isolated Mitochondria and Submitochondrial Particles of Beef Heart Muscle . J Cell Biol 1 July 1964; 22 (1): 63–100. doi: https://doi.org/10.1083/jcb.22.1.63
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