Study on the Cellular Regulation and Function of Lysine Malonylation, Glutarylation and Crotonylation: Springer Theses
Autor Xiucong Baoen Limba Engleză Hardback – 21 mar 2020
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Specificații
ISBN-13: 9789811525087
ISBN-10: 9811525080
Ilustrații: XVIII, 163 p. 132 illus., 96 illus. in color.
Dimensiuni: 155 x 235 mm
Greutate: 0.44 kg
Ediția:1st ed. 2020
Editura: Springer Nature Singapore
Colecția Springer
Seria Springer Theses
Locul publicării:Singapore, Singapore
ISBN-10: 9811525080
Ilustrații: XVIII, 163 p. 132 illus., 96 illus. in color.
Dimensiuni: 155 x 235 mm
Greutate: 0.44 kg
Ediția:1st ed. 2020
Editura: Springer Nature Singapore
Colecția Springer
Seria Springer Theses
Locul publicării:Singapore, Singapore
Cuprins
Introduction to Protein Posttranslational Modifications (PTMs).- Chemical reporter for Lysine Malonylation.- Identification of Histone Lysine Glutarylation.- Glutarylation at Histone H4 lysine 91 Modulates Chromatin Assembly.- Identification of Sirt3 as an ‘Eraser’ for Histone Lysine Crotonylation Marks using a Chemical Proteomics Approach.
Textul de pe ultima copertă
This book presents pioneering findings on the characterization of cellular regulation and function for three recently identified protein posttranslational modifications (PTMs): lysine malonylation (Kmal), glutarylation (Kglu) and crotonylation (Kcr). It addresses three main topics: (i) Detecting Kmal substrates using a chemical reporter, which provides important information regarding the complex cellular networks modulated by Kmal; (ii) Identifying Kglu as a new histone PTM and assessing the direct impact of histone Kglu on chromatin structure and dynamics; and (iii) Revealing Sirt3’s value as a regulating enzyme for histone Kcr dynamics and gene transcription, which opens new avenues for examining the physiological significance of histone Kcr. Taken together, these studies provide information critical to understanding how these protein PTMs are associated with various human diseases, and to identifying therapeutic targets for the dysregulation of these novel protein markers in varioushuman diseases.
Caracteristici
Nominated as an outstanding Ph.D. thesis by the University of Hong Kong Reports on important advances in the study of histone posttranslational modifications (PTMs) Introduces applications of the CLASPI approach in identifying ‘eraser’ enzymes for histone PTMs Discusses chemical reporters for protein posttranslational modifications Unravels the role of histone modifications in the regulation of chromatin structure