Pregled bibliografske jedinice broj: 830320
The Use of the Miyazawa-Jernigan Residue Contact Potential in Analyses of Molecular Interaction and Recognition with Complementary Peptides
The Use of the Miyazawa-Jernigan Residue Contact Potential in Analyses of Molecular Interaction and Recognition with Complementary Peptides // IWBBIO 2016, Lecture Notes in Bioinformatics 9656 / Ortuño, Francisco ; Rojas, Ignacio (ur.).
Cham: Springer, 2016. str. 91-102 (predavanje, međunarodna recenzija, cjeloviti rad (in extenso), znanstveni)
CROSBI ID: 830320 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The Use of the Miyazawa-Jernigan Residue Contact Potential in Analyses of Molecular Interaction and Recognition with Complementary Peptides
Autori
Štambuk, Nikola ; Konjevoda, Paško ; Manojlović, Zoran ; Novak Kujundžić, Renata
Vrsta, podvrsta i kategorija rada
Radovi u zbornicima skupova, cjeloviti rad (in extenso), znanstveni
Izvornik
IWBBIO 2016, Lecture Notes in Bioinformatics 9656
/ Ortuño, Francisco ; Rojas, Ignacio - Cham : Springer, 2016, 91-102
ISBN
978-3-319-31743-4
Skup
4th International Work-Conference on Bioinformatics and Biomedical Engineering (IWBBIO 2016)
Mjesto i datum
Granada, Španjolska, 20.04.2016. - 22.04.2016
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
contact; potential; protein-protein; interaction; peptide; binding
Sažetak
The classic results by Biro, Blalock and Root-Bernstein link genetic code nucleotide patterns to amino acid properties, protein structure and interaction. This study explores the use of the Miyazawa-Jernigan residue contact potential in analyses of protein interaction and recognition between sense and complementary (antisense) peptides. We show that Miyazawa-Jernigan residue contact energies, derived from 3D data, define the recognition rules of peptide-peptide interaction based on the complementary coding of DNA and RNA sequences. The model is strongly correlated with several other chemoinformatic scales often used for the determination of protein antigenic sites and transmembrane regions (Parker et al. r = 0.94 ; Rose et al. r = − 0.92 ; Manavalan-Ponnuswamy r = − 0.92 ; Cornette et al. r = − 0.91 ; Kolaskar-Tongaonkar r = − 0.91 ; Grantham r = 0.90 ; White-Wimley (octanol) r = − 0.88 ; Kyte-Doolittle r = − 0.85). The algorithms presented have important biomedical and proteomic applications related to modulation of the peptide-receptor function and epitope-paratope interaction, the design of lead compounds and the development of new immunochemical assays and diagnostic procedures.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
098-0982929-2524 - Modeliranje bioaktivnih molekula i ispitivanje njihovih svojstava i učinka (Štambuk, Nikola, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus