The mechanism of nuclear transport of natural or artificial transport substrates in digitonin-permeabilized cells

I. Cserpan, A. Udvardy

Research output: Contribution to journalArticle

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Abstract

Characterization of nuclear protein transport in digitonin-permeabilized cells revealed that the number of the nuclear localization signal sequences (NLS) within the transport substrate basically influences the mechanism of the transport reaction. Phycoerythrine-NLS transport substrate carrying a maximum of 4.5 conjugated NLSs/subunit, or Bsp methyltransferase-NLS fusion protein were efficiently transported into the nuclei of digitonin-permeabilized cultured cells without any exogenously added cytosolic protein. All the characteristic properties of in vivo nuclear transport are faithfully reproduced with these transport substrates: (i) the transport requires a functional NLS in the transported protein, a transport-incompetent mutant NLS being ineffective; (ii) the transport is energy dependent; (iii) the wild type nuclear localization peptide efficiently competes for transport, while the transport-incompetent mutant peptide does not; and (iv) wheat germ agglutinin inhibits this transport reaction. Nuclear transport observed with these substrates was not due to any damage of the nuclear membrane or inefficient extraction of the cytosolic proteins during the permeabilization of the cells. The nuclear transport was proportional to the number of conjugated NLSs. Nuclear transport of phycoerythrine carrying 7-8 conjugated NLSs/subunit required the addition of exogenous cytosolic proteins. This transport also fulfilled all the characteristic properties of an authentic nuclear transport. Nuclear transport with different combinations of transport substrates further supported the assumption that distinct transport mechanisms operate for different substrates. From a mixture of PE-NLS7.8 and Bsp methyltransferase-NLS, the highly conjugated substrate was completely retained in the cytoplasm in the absence of exogenous cytosol, while Bsp methyltransferase-NLS was efficiently transported. Exogenous cytosol promoted the nuclear transport of the highly conjugated substrate.

Original languageEnglish
Pages (from-to)1849-1861
Number of pages13
JournalJournal of Cell Science
Volume108
Issue number5
Publication statusPublished - 1995

Fingerprint

Digitonin
Cell Nucleus Active Transport
Nuclear Localization Signals
Protein Sorting Signals
Methyltransferases
Protein Transport
Cytosol
Proteins
Peptides
Wheat Germ Agglutinins
Nuclear Envelope
Nuclear Proteins
Cultured Cells
Cytoplasm
Cell Count

Keywords

  • Digitonin permeabilization
  • Nuclear localization signal
  • Nuclear transport

ASJC Scopus subject areas

  • Cell Biology

Cite this

The mechanism of nuclear transport of natural or artificial transport substrates in digitonin-permeabilized cells. / Cserpan, I.; Udvardy, A.

In: Journal of Cell Science, Vol. 108, No. 5, 1995, p. 1849-1861.

Research output: Contribution to journalArticle

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