Preparation and Crystallization of Picornain 3C of Rhinovirus A28

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

Human rhinovirus picornain 3C is a high-value commercial cysteine protease, which is widely used to remove affinity tags and fusion proteins during the purification of the target proteins. A variant of rhinovirus A28 picornain 3C produced in this study is not annotated in the NCBI databases, shares 79% sequence identity in the PDB, and was not previously used in the protein engineering. A protocol was developed for the isolation and purification of the protein to use it in structural studies. The initial crystallization conditions were found. The determination and analysis of the structure of rhinovirus A28 picornain 3C will provide new possibilities for performing basic research on the evolution of proteolytic enzymes and for the design of the optimal variant of this protease.

Авторлар туралы

A. Tishin

State Research Center of Virology and Biotechnology “Vector,” Rospotrebnadzor, 630559, Koltsovo, Novosibirsk oblast, Russia

Email: gladysheva_av@vector.nsc.ru
Россия, Кольцово

A. Gladysheva

State Scientific Center of Virology and Biotechnology «Vector»

Email: gladysheva_av@vector.nsc.ru
ORCID iD: 0000-0002-7396-3954
SPIN-код: 5214-3421
Scopus Author ID: 57194590629

Postgraduate student, Juniour Researcher, Department of Molecular Virology for Flaviviruses and Viral Hepatitis

Ресей, 630559, Novosibirsk region, Koltsovo

L. Pyatavina

State Research Center of Virology and Biotechnology “Vector,” Rospotrebnadzor, 630559, Koltsovo, Novosibirsk oblast, Russia; Novosibirsk National Research State University, 630090, Novosibirsk, Russia

Email: gladysheva_av@vector.nsc.ru
Россия, Кольцово; Россия, Новосибирск

S. Olkin

State Research Center of Virology and Biotechnology “Vector,” Rospotrebnadzor, 630559, Koltsovo, Novosibirsk oblast, Russia

Email: gladysheva_av@vector.nsc.ru
Россия, Кольцово

A. Gladysheva

State Scientific Center of Virology and Biotechnology «Vector»; Novosibirsk National Research State University

Email: gladysheva_aa@vector.nsc.ru
ORCID iD: 0000-0002-9490-1939

Graduate student, Assistant, Department of Molecular Virology for Flaviviruses and Viral Hepatitis

Ресей, 630559, Novosibirsk region, Koltsovo; 630090, Novosibirsk

I. Imatdionov

State Research Center of Virology and Biotechnology “Vector,” Rospotrebnadzor, 630559, Koltsovo, Novosibirsk oblast, Russia

Email: gladysheva_av@vector.nsc.ru
Россия, Кольцово

A. Vlaskina

National Research Centre “Kurchatov Institute”, 123098, Moscow, Russia

Email: gladysheva_av@vector.nsc.ru
Россия, Москва

A. Nikolaeva

National Research Centre “Kurchatov Institute”, 123098, Moscow, Russia

Email: gladysheva_av@vector.nsc.ru
Россия, Москва

V. Samygina

National Research Centre “Kurchatov Institute”, 123182, Moscow, Russia; Shubnikov Institute of Crystallography, Federal Scientific Research Centre “Crystallography and Photonics,” Russian Academy of Sciences, 119333, Moscow, Russia

Email: lera@crys.ras.ru
Россия, Москва; Россия, Москва

A. Agafonov

State Research Center of Virology and Biotechnology “Vector,” Rospotrebnadzor, 630559, Koltsovo, Novosibirsk oblast, Russia

Хат алмасуға жауапты Автор.
Email: gladysheva_av@vector.nsc.ru
Россия, Кольцово

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© А.Е. Тишин, А.В. Гладышева, Л.А. Пятавина, С.Е. Олькин, А.А. Гладышева, И.Р. Иматдинов, А.В. Власкина, А.Ю. Николаева, В.Р. Самыгина, А.П. Агафонов, 2023

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