Broad pore lifetime distributions: A fundamental concept for cell electroporation
Julie V. Stern, Thiruvallur R. Gowrishankar, Kyle C. Smith, and James, C. Weaver

TL;DR
This paper introduces the concept of broad pore lifetime distributions in cell electroporation, emphasizing the creation of diverse pore structures with varying lifetimes, challenging the traditional single-lifetime model.
Contribution
It proposes a complex model of pore formation involving multiple pore types with a wide range of lifetimes, supported by experimental implications.
Findings
Pore lifetimes range from ~100 ns to 1,000 s.
Most pores are short-lived, with few lasting long.
Traditional methods may miss most pores due to rapid lifetime falloff.
Abstract
We describe a concept that has the potential to change how we think about the underlying mechanisms of cell membrane electroporation (EP). Prior experimental, theoretical and modeling have emphasized a single pore lifetime as adequate for particular conditions. Here we introduce a much more complex response: The rapid creation of many types of pore structures, of which some are traditional transient lipidic pores (TPs), but the great majority are complex pores (CPs) based on both lipids and other molecules or molecular segments. At the inner leaflet of the cell plasma membrane (PM) non-lipidic molecules come from the over-crowded cytoplasm. At the outer leaflet they originate from the extracellular medium and extracellular matrix. Some partially or fully insert into TPs during or shortly after TP formation, or bind to the membrane nearby. This process is complex, leading to mostly…
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Taxonomy
TopicsMicrobial Inactivation Methods · Plasma Applications and Diagnostics
