The Functionality of Membrane-Inserting Proteins and Peptides: Curvature Sensing, Generation, and Pore Formation

被引:4
|
作者
Has, Chandra [1 ]
Das, Sovan Lal [1 ]
机构
[1] GSFC Univ, Dept Chem Engn, Vadodara 391750, Gujarat, India
来源
JOURNAL OF MEMBRANE BIOLOGY | 2023年 / 256卷 / 4-6期
关键词
Membrane curvature; Hydrophobic insertion; Antimicrobial peptides; Membrane pore formation; INTRINSICALLY DISORDERED REGIONS; HUMAN ANTIMICROBIAL PEPTIDE; ATOMIC-FORCE MICROSCOPY; VOLTAGE-SENSOR TOXIN; PRECURSOR LIPID II; X-RAY-DIFFRACTION; BAR DOMAINS; AMPHIPATHIC HELICES; HYDROPHOBIC MISMATCH; MOLECULAR-MECHANISM;
D O I
10.1007/s00232-023-00289-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins and peptides with hydrophobic and amphiphilic segments are responsible for many biological functions. The sensing and generation of membrane curvature are the functions of several protein domains or motifs. While some specific membrane proteins play an essential role in controlling the curvature of distinct intracellular membranes, others participate in various cellular processes such as clathrin-mediated endocytosis, where several proteins sort themselves at the neck of the membrane bud. A few membrane-inserting proteins form nanopores that permeate selective ions and water to cross the membrane. In addition, many natural and synthetic small peptides and protein toxins disrupt the membrane by inducing nonspecific pores in the membrane. The pore formation causes cell death through the uncontrolled exchange between interior and exterior cellular contents. In this article, we discuss the insertion depth and orientation of protein/peptide helices, and their role as a sensor and inducer of membrane curvature as well as a pore former in the membrane. We anticipate that this extensive review will assist biophysicists to gain insight into curvature sensing, generation, and pore formation by membrane insertion.
引用
收藏
页码:343 / 372
页数:30
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