PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 1, 1986Journal of Biological Chemistry214 citationsOpen Access

Membrane damage by hemolytic viruses, toxins, complement, and other cytotoxic agents. A common mechanism blocked by divalent cations.

View Full Paper
CBC.L. BashfordGAG.M. AlderGMGianfranco Menestrina

Key Points

Key points are not available for this paper at this time.

Abstract

Hemolytic viruses, bacterial and animal toxins, the components of activated complement, cationic proteins, and detergents induce a sequence of permeability changes at the plasma membrane that are in every case sensitive to changes in ionic strength and to divalent cations. Individually, each agent exhibits positive cooperativity; when two agents are present together, they show synergy. It is concluded that such cytotoxic agents damage membranes by a common mechanism. Hence permeability changes are unlikely to depend on the formation of specific, protein-lined channels, as previously envisaged in the case of activated complement or certain bacterial toxins.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Bashford et al. (1986) studied this question.

synapsesocial.com/papers/6a2506b5055282ef55fecd97https://doi.org/10.1016/s0021-9258(18)67654-9
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Sequenzanalyse des Melittins aus den tryptischen und peptischen Spaltstücken1967 · 339 citations
  2. 2Cell damage by viruses, toxins and complement: common features of pore-formation and its inhibition by Ca2+.1985 · 29 citations
  3. 3The recovery of human polymorphonuclear leucocytes from sublytic complement attack is mediated by changes in intracellular free calcium1985 · 134 citations
  4. 4Reconstruction of biological membranes.1972 · 296 citations
  5. 5Structural changes in membranes produced by the binding of small amphipathic molecules1984 · 81 citations