Detailed Information on Publication Record
2019
Microscopy examination of red blood and yeast cell agglutination induced by bacterial lectins
MRÁZKOVÁ, Jana, Lenka MALINOVSKÁ and Michaela WIMMEROVÁBasic information
Original name
Microscopy examination of red blood and yeast cell agglutination induced by bacterial lectins
Authors
MRÁZKOVÁ, Jana (203 Czech Republic, belonging to the institution), Lenka MALINOVSKÁ (203 Czech Republic, belonging to the institution) and Michaela WIMMEROVÁ (203 Czech Republic, guarantor, belonging to the institution)
Edition
PLOS ONE, Public Library of Science, 2019, 1932-6203
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.740
RIV identification code
RIV/00216224:14740/19:00107577
Organization unit
Central European Institute of Technology
UT WoS
000484977900081
Keywords in English
lectins; microscopy; agglutination; specificity
Tags
International impact, Reviewed
Změněno: 27/10/2024 15:04, Ing. Martina Blahová
Abstract
V originále
Lectins are a group of ubiquitous proteins which specifically recognize and reversibly bind sugar moieties of glycoprotein and glycolipid constituents on cell surfaces. The mutagenesis approach is often employed to characterize lectin binding properties. As lectins are not enzymes, it is not easy to perform a rapid specificity screening of mutants using chromogenic substrates. Lectin-based cell agglutination is a simple and low-cost technique which can overcome most of these problems. In this work, a modified method of the agglutination of human erythrocytes and yeast cells with microscopy detection was successfully used for a specificity study of the newly prepared mutant lectin RS-IIL_A22S, which experimentally completed studies on sugar preferences of lectins in the PA-IIL family. Results showed that the sensitivity of this method is comparable with ITC, is able to determine subtle differences in lectin specificity, and works directly in cell lysates.
Links
GA18-18964S, research and development project |
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LQ1601, research and development project |
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MUNI/A/1575/2018, interní kód MU |
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90043, large research infrastructures |
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