1. Academic Validation
  2. A nuclear RNA-binding cyclophilin in human T cells

A nuclear RNA-binding cyclophilin in human T cells

  • FEBS Lett. 1996 Dec 2;398(2-3):201-5. doi: 10.1016/s0014-5793(96)01248-3.
H Mi 1 O Kops E Zimmermann A Jäschke M Tropschug
Affiliations

Affiliation

  • 1 Institut für Biochemie und Molekularbiologie der Albert-Ludwigs-Universität, Freiburg, Germany.
Abstract

Cyclophilins (CyPs) are binding proteins for the immunosuppressive drug cyclosporin A (CsA). CyPs are evolutionarily highly conserved proteins present in both pro- and eukaryotes as well as in different subcellular locations. CyPs possess enzymatic activity, namely peptidyl-prolyl cis-trans isomerase (PPIase) activity; CyPs are involved in cellular protein folding and protein interactions. To date, only cyclosporins and proteins are known to interact with CyPs. Here we describe a novel nuclear Cyclophilin (hCyP33) from human T cells with an additional RNA-binding domain. This combines for the first time RNA binding and protein folding in one protein.

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