Predicting Structure and Function of Membrane Polypeptides
Main researcher
: JURETIĆ, DAVOR (19290) Assistants
Type of research: basic Duration from: 01/01/91. to 12/31/96. Papers on project (total): 30
Papers on project quoted in Current Contents: 15
Institution name: Fakultet prirodoslovno matematičkih znanosti i odgojnih područja, Split (177) Department/Institute: Department of Physics, Natural Sciencies and Arts Department, University of Split Address: N. Tesle 12 City: 21000 - Split, Croatia
Communication
Phone: 385 (0)21587133
Phone: 385 (0)21591438
Phone: 385 (0)21587009
Fax: 385 (0)21362431
E-mail: juretic"mapmf.pmfst.hr
Summary: Several theoretical methods for predicting structure and
function of membrane-bound peptides and proteins will be developed. Our
development of one new possibility for predicting protein secondary
structure, based on the introduction of preference functions, will make
possible to achieve high accuracy in predicting secondary structure of
integral membrane proteins. Preference functions are introduced in the
predictive algorithm as functions of geometrical, statistical or physical
folding parameters. Optimal folding parameters and optimal performance
parameters will be found during next stage of this work. The work is also
in progress in collecting new evidence that group of recently dicovered
membrane-active peptide antibiotics, called magainins, is acting
reversibly, cooperatively and sinergeticaly in decreasing the membrane
potential of cytochrome c oxidase liposomes. Nonlinear kinetic models for
the activity of membrane-bound proton pumps, such as cytochrome c oxidase,
will be also examined.
Research goals: Several theoretical methods for predicting structure
and functionof membrane-bound peptides and proteins will be
developed.Expected results are better understanding how folding motifs
inmembrane-bound polypeptides emerge during protein folding processin
membrane environment and how such polypeptides perform theirperturbing or
beneficial function. During past three years, themethod, named preference
functions method, has been developed inour laboratory and shown to be
competitive with the bestavailable methods for predicting secondary
structure of membraneproteins. Research goal in the next period will be to
findoptimal conformational parameters, performance parameters andprotein
data bases for standard applications of our predictionscheme. The
structure and function of membrane-active peptides,such as magainins, will
be further examined, in the light of ourdiscovery that membrane-bound
magainin oligomers reversiblyinhibit cellular free-energy transduction.
Quantitative structure-activity and structure-physical property
relationships will befound for some small peptides. Nonlinear kinetic
models forcytochrome c oxidase proton pumping activity with
variableintrinsic uncoupling will be also constructed.
COOPERATION - INSTITUTIONS
Name of institution
: Institut "Ruđer Bošković" Type of institution: University/Faculty Type of cooperation: Joint publishing of scientific papers City: 10000 - Zagreb, Croatia
OTHER ACHIEVEMENTS
Name
: Paketi FORTRAN programa PREF 2.0 i PREF 3.0 (PREF-SPLIT) Type of achievement: Other Authors: Davor Juretić, Bono Lučić
Name
: CROPROT datoteka od oko 200 integralnih membranskih
proteina Type of achievement: Other Authors: Davor Juretić, Bono Lučić
Name
: JURAAS datoteka od oko 100 skala svojstava aminokiselina Type of achievement: Other Authors: Davor Juretić Other information about the project.