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Protein Modification and Autophagy Activation

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 1206))

Abstract

Protein modification refers to the chemical modification of proteins after their biosynthesis, which is also called posttranslational modification (PTM). PTM causes changes in protein properties and functions. PTM includes an attachment of addition of functional groups, such as methylation, acetylation, glycosylation and phosphorylation; a covalent coupling of small peptides or proteins, such as ubiquitination and SUMOylation; or chemical changes in amino acids, such as citrullination (conversion of arginine to citrulline). Protein modification plays an important role in cellular processes. Since a protein can be modified in different ways, such as acetylation, methylation and phosphorylation, the functions of proteins are different under different modification states. Moreover, the same modification at different sites may have completely different effects on protein function. For example, phosphorylation at some sites in a protein may lead to a functional activation, while phosphorylation at other sites may cause an inhibition of the functions. Thus, different modifications, combinations and sites changes lead to different functional regulations of a protein, resulting in different effects in the cells. In autophagy, PTMs are widely involved in the regulation of autophagy, including ubiquitination, phosphorylation and acetylation. Ubiquitination is the covalent conjugation of ubiquitin to the substrates through a series of enzymes. Phosphorylation refers to an attachment of a phosphoryl group into a protein, primarily on serine, threonine and tyrosine, which is catalyzed by the kinases. Phosphorylation, a common modification, regulates protein function and localization. Phosphorylation in autophagy regulates the activity of autophagy-associated proteins and the initiation and progression of autophagy by regulating signaling pathways. Acetylation means the addition of acetyl groups onto lysine or N-terminal segment of target proteins through acetyltransferases. Acetylation and deacetylation are both involved in the regulation of autophagy initiation and selective autophagy by controlling the acetylation level of important proteins in the autophagy process. In this chapter, we will focus on the regulation of ubiquitination and phosphorylation in autophagy.

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Abbreviations

ALS:

Autophagy-lysosome system

AMPK:

AMP-regulated protein kinase

CC:

Coiled-coil domain

CTD:

C-terminal domain

Cvt:

Cytoplasm-to-vacuole target

E1:

Ubiquitin-activating enzyme

E2:

Ubiquitin-conjugating enzyme

E3:

Ubiquitin ligase

HDAC6:

Histone deacetylase 6

LIR:

LC3-interacting region

MAPK:

Mitogen-activated protein kinase

NBR1:

Neighbor of breast cancer 1

OPTN:

Optineurin

PAS:

Pre-autophagosomal structure

PE:

Phosphatidylethanolamine

PI:

PtdIns

PI3KC3:

PI3K class III complex

PI3P:

PtdIns3P

PKC:

Protein kinase C

PP:

Protein phosphatase

PS:

Proline/serine-rich

TORC1:

Target of rapamycin complex 1

TSC2:

Tuberous sclerosis complex 2

Ub:

Ubiquitin

UBA:

Ubiquitin-associated

ULK:

Unc-51-like kinase

UPS:

Ubiquitin-proteasome system

ZZ:

Zinc finger

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Correspondence to Guanghui Wang .

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Wang, R., Wang, G. (2019). Protein Modification and Autophagy Activation. In: Qin, ZH. (eds) Autophagy: Biology and Diseases. Advances in Experimental Medicine and Biology, vol 1206. Springer, Singapore. https://doi.org/10.1007/978-981-15-0602-4_12

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