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Aggregation of Human Wild-Type and H27A-Prolactin in Cells and in Solution: Roles of Zn²⁺, Cu²⁺, and pH

Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520

Address all correspondence and requests for reprints to: Dr. Priscilla S. Dannies, Department of Pharmacology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520-8066. E-mail: . priscilla.dannies{at}yale.edu

Aggregation of hormones is an important step in the formation of secretory granules that results in concentration of hormones. In transfected AtT20 cells, but not COS cells, Lubrol-insoluble aggregates of human prolactin (PRL) accumulated within 30 min after synthesis. Aggregation in AtT20 cells was reduced by incubation with 30 µM chloroquine, which neutralizes intracellular compartments, and was slowed by incubation with diethyldithiocarbamate, which chelates Cu²⁺ and Zn²⁺. H27A-PRL aggregated in AtT20 cells as well as wild-type PRL, indicating that a high affinity Zn²⁺-binding site is not necessary. In solution, purified recombinant human PRL was precipitated by 20 µM Cu²⁺ or Zn²⁺. In solution without polyethylene glycol there was no precipitation with acidic pH alone, precipitation with Zn²⁺ was most effective at neutral pH, and the ratio of Zn²⁺ to PRL was greater than 1 in the precipitate. In solution with polyethylene glycol, precipitation occurred with acidic pH, precipitation with Zn²⁺ occurred effectively at acidic pH, and the ratio of Zn²⁺ to PRL was less than 1. The aggregates obtained in polyethylene glycol are therefore better models for aggregates in cells. Unlike human PRL, aggregation of rat PRL has been shown to occur at neutral pH in cells and in solution, and therefore these two similar proteins form aggregates that are the cores of secretory granules in ways that are not completely identical.

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