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L PACKER

Publications and source records attributed to L PACKER.

At least 19 recordsLinked to original sources
PubMed1963

SIZE AND SHAPE TRANSFORMATIONS CORRELATED WITH OXIDATIVE PHOSPHORYLATION IN MITOCHONDRIA. I. SWELLING-SHRINKAGE MECHANISMS IN INTACT MITOCHONDRIA.

Two types of swelling-shrinkage change manifested by isolated mammalian heart mitochondria have been studied. One type, designated as phase I or "low amplitude" swelling-shrinkage, is estimated to lead to changes in mitochondrial volume of 20 to 40 per cent, to changes in light scattering of about 30 per cent, and to changes in viscosity. These physical changes in mitochondria are brought about rapidly and reversibly by normal reactants of the respiratory chain. Their speed, specificity, and reversibility indicate that they are closely geared to the normal function of the respiratory chain and are a true reflection of a mechanochemical coupling process characteristic of the physiology of mitochondria. A second type of swelling-shrinkage mechanism, designated as phase II or "high amplitude," leads to changes in light scattering, viscosity, and mitochondrial volume which, frequently but not always, are of higher magnitude than the phase I type. Phase II swelling-shrinkage seems to be only partly under the control of the respiratory chain. Prior to the completion of phase II swelling, a stepwise loss of mitochondrial function can be identified, such as changes in the rate of substrate utilization and loss of respiratory control. Reversal of this type of swelling cannot be effected if the swelling change reaches a steady state. This type of swelling may provide cells with a mechanism for destroying mitochondrial substance.

Animals↗
PubMed1963

SIZE AND SHAPE TRANSFORMATIONS CORRELATED WITH OXIDATIVE PHOSPHORYLATION IN MITOCHONDRIA. II. STRUCTURAL CHANGES IN MITOCHONDRIAL MEMBRANE FRAGMENTS.

It has been demonstrated that the nature of the physical change in mitochondrial membrane fragments associated with the action of the respiratory enzymes is likely one of shape or symmetry rather than size. The findings suggest that in the state of decreased scattering the macromolecules may be present in an extended physical state. Conditions favorable for phosphorylation may give rise to a folding or contraction of the molecular complex to a more symmetrical structure. Since earlier studies have shown that there is a compulsory relationship between the integrity of systems operative in oxidative phosphorylation and scattering changes, experiments of this type may lead to values for the minimal size of a phosphorylating unit, which at present is estimated to be 2.1 x 10(6) from light-scattering studies.

Metabolism↗