1. Academic Validation
  2. DHHC2 is a protein S-acyltransferase for Lck

DHHC2 is a protein S-acyltransferase for Lck

  • Mol Membr Biol. 2011 Oct-Nov;28(7-8):473-86. doi: 10.3109/09687688.2011.630682.
Ruth Zeidman 1 Gemma Buckland Marek Cebecauer Philipp Eissmann Daniel M Davis Anthony I Magee
Affiliations

Affiliation

  • 1 Molecular Medicine Section, National Heart & Lung Institute, Imperial College London, Sir Alexander Fleming Building, South Kensington, London, UK.
Abstract

Lck is a non-receptor tyrosine kinase of the Src family that is essential for T cell activation. Dual N-terminal acylation of Lck with myristate (N-acylation) and palmitate (S-acylation) is essential for its membrane association and function. Reversible S-acylation of Lck is observed in vivo and may function as a control mechanism. Here we identify the DHHC family protein S-acyltransferase DHHC2 as an Enzyme capable of palmitoylating of Lck in T cells. Reducing the DHHC2 level in Jurkat T cells using siRNA causes decreased Lck S-acylation and partial dislocation from membranes, and conversely overexpression of DHHC2 increases S-acylation of an Lck surrogate, LckN10-GFP. DHHC2 localizes primarily to the endoplasmic reticulum and Golgi apparatus suggesting that it is involved in S-acylation of newly-synthesized or recycling Lck involved in T cell signalling.

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