Synthesis and characterization of fluorogenic peptide substrate of HIV-1 protease based on fluorescence resonance energy transfer

Synthesis of fluorogenic peptide substrate of HIV-I protease Dns-SQNYPIVWL which corresponds to the p17/p24 cleavage site for HIV-l protease have been performed. This fluorogenic substrate was based on the fluorescence resonance energy transfer between donor – Trp residue, and acceptor – dansyl grou...

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Бібліографічні деталі
Дата:1995
Автори: Kornelyuk, A.I., Terentiev, A.G., Fisher, S., Porter, T.
Формат: Стаття
Мова:English
Опубліковано: Інститут молекулярної біології і генетики НАН України 1995
Назва видання:Биополимеры и клетка
Онлайн доступ:http://dspace.nbuv.gov.ua/handle/123456789/156188
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Synthesis and characterization of fluorogenic peptide substrate of HIV-1 protease based on fluorescence resonance energy transfer / A.L. Kornelyuk, A.G. Terentiev, S. Fisher, T. Porter // Биополимеры и клетка. — 1995. — Т. 11, № 6. — С. 57-61. — Бібліогр.: 18 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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Резюме:Synthesis of fluorogenic peptide substrate of HIV-I protease Dns-SQNYPIVWL which corresponds to the p17/p24 cleavage site for HIV-l protease have been performed. This fluorogenic substrate was based on the fluorescence resonance energy transfer between donor – Trp residue, and acceptor – dansyl group in the intact peptide. Hydrolysis of substrate by recombinant HIV-I protease resulted in the time-dependent increase of Trp fluorescence and decrease of dansyl fluorescence measured at 350 and 500 nm, respectively, due to the break of resonance energy transfer between donor and acceptor fluorophors. Hydrolysis of fluorogenic peptide substrate was studied also by reversed phase HPLC and two peptide fragments after cleavage of substrate have been detected. Kinetic constants of hydrolysis for this fluorogenic peptide substrate by HIV-I protease were calculated from Lineweaver – Burk plots: KM - 29mkM, kcat =5.4 s⁻¹ and kcat / KM -180000 M⁻¹s⁻¹.