Specificity in pleckstrin homology (PH) domain membrane targeting: a role for a phosphoinositide-protein co-operative mechanism

FEBS Lett. 2001 Oct 12;506(3):173-9. doi: 10.1016/s0014-5793(01)02909-x.

Abstract

Pleckstrin homology (PH) domains are protein modules found in proteins involved in many cellular processes. The majority of PH domain-containing proteins require membrane association for their function. It has been shown that most PH domains interact directly with the cell membrane by binding to phosphoinositides with a broad range of specificity and affinity. While a highly specific binding of the PH domain to a phosphoinositide can be necessary and sufficient for the correct recruitment of the host protein to the membrane, a weaker and less specific interaction may be necessary but not sufficient, thus probably requiring alternative, co-operative mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Blood Proteins / chemistry*
  • Isoenzymes / chemistry
  • Isoenzymes / metabolism
  • Models, Molecular
  • Phosphatidylinositols / metabolism*
  • Phospholipase C delta
  • Phosphoproteins / chemistry*
  • Protein Binding
  • Proteins / metabolism*
  • Type C Phospholipases / chemistry
  • Type C Phospholipases / metabolism

Substances

  • Blood Proteins
  • Isoenzymes
  • Phosphatidylinositols
  • Phosphoproteins
  • Proteins
  • platelet protein P47
  • Type C Phospholipases
  • Phospholipase C delta