Peter Tompa

Prof. Peter Tompa

orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2002 in Trends in Biochemical Sciences
Verified
Journal Article
Closed access
PTPeter Tompa
Peter Tompa

1 January 2008 in Trends in Biochemical Sciences
Verified
Journal Article
Closed access
PTPeter Tompa
Peter Tompa
MFMonika Fuxreiter
Monika Fuxreiter


1 August 2004 in The FASEB Journal
Verified
Journal Article
Closed access
PTPeter Tompa
Peter Tompa
PCPeter Csermely
Peter Csermely

1 September 2005 in Trends in Biochemical Sciences
Verified
Journal Article
Closed access
PTPeter Tompa
Peter Tompa
CSCsilla Szász
Csilla Szász
LBLászló Buday
László Buday

21 March 2008 in Plant Physiology
Verified
Journal Article
Closed access
DKDenes Kovacs
Denes Kovacs
EKEva Kalmar
Eva Kalmar
ZTZsolt Torok
Zsolt Torok
PTPeter Tompa
Peter Tompa
ERD10 and ERD14 (for early response to dehydration) proteins are members of the dehydrin family that accumulate in response to abiotic environmental stresses, such as high salinity, drought, and low temperature, in Arabidopsis (Arabidopsis thaliana). Whereas these proteins protect cells against the consequences of dehydration, the exact mode(s) of their action remains poorly understood. Here, detailed evidence is provided that ERD10 and ERD14 belong to the family of intrinsically disordered proteins, and it is shown in various assays that they act as chaperones in vitro. ERD10 and ERD14 are able to prevent the heat-induced aggregation and/or inactivation of various substrates, such as lysozyme, alcohol dehydrogenase, firefly luciferase, and citrate synthase. It is also demonstrated that ERD10 and ERD14 bind to acidic phospholipid vesicles without significantly affecting membrane fluidity. Membrane binding is strongly influenced by ionic strength. Our results show that these intrinsically disordered proteins have chaperone activity of rather wide substrate specificity and that they interact with phospholipid vesicles through electrostatic forces. We suggest that these findings provide the rationale for the mechanism of how these proteins avert the adverse effects of dehydration stresses.