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细胞-细胞交配相互作用:单细胞力谱学的概述与潜力。

Cell-Cell Mating Interactions: Overview and Potential of Single-Cell Force Spectroscopy.

机构信息

Biology Department, Brooklyn College of the City University of New York, 2900 Bedford Avenue, Brooklyn, NY 11210, USA.

Department of Sciences, John Jay College of the City University of New York, New York, NY 10019, USA.

出版信息

Int J Mol Sci. 2022 Jan 20;23(3):1110. doi: 10.3390/ijms23031110.


DOI:10.3390/ijms23031110
PMID:35163034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8835621/
Abstract

It is an understatement that mating and DNA transfer are key events for living organisms. Among the traits needed to facilitate mating, cell adhesion between gametes is a universal requirement. Thus, there should be specific properties for the adhesion proteins involved in mating. Biochemical and biophysical studies have revealed structural information about mating adhesins, as well as their specificities and affinities, leading to some ideas about these specialized adhesion proteins. Recently, single-cell force spectroscopy (SCFS) has added important findings. In SCFS, mating cells are brought into contact in an atomic force microscope (AFM), and the adhesive forces are monitored through the course of mating. The results have shown some remarkable characteristics of mating adhesins and add knowledge about the design and evolution of mating adhesins.

摘要

可以毫不夸张地说,交配和 DNA 转移是生物体的关键事件。在促进交配所需的特征中,配子之间的细胞黏附是普遍的要求。因此,参与交配的黏附蛋白应该具有特定的性质。生化和生物物理研究揭示了关于交配黏附素的结构信息,以及它们的特异性和亲和力,从而对这些特殊的黏附蛋白有了一些认识。最近,单细胞力谱学(SCFS)提供了重要的发现。在 SCFS 中,将交配细胞放入原子力显微镜(AFM)中接触,并在交配过程中监测黏附力。结果表明了交配黏附素的一些显著特征,并增加了对交配黏附素设计和进化的了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/0ec18f33f4d0/ijms-23-01110-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/0da5a7f5e0f8/ijms-23-01110-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/2f08a7270375/ijms-23-01110-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/d3a90f5a12fe/ijms-23-01110-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/0ec18f33f4d0/ijms-23-01110-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/0da5a7f5e0f8/ijms-23-01110-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/2f08a7270375/ijms-23-01110-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/d3a90f5a12fe/ijms-23-01110-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a581/8835621/0ec18f33f4d0/ijms-23-01110-g004.jpg

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本文引用的文献

[1]
N501Y mutation of spike protein in SARS-CoV-2 strengthens its binding to receptor ACE2.

Elife. 2021-8-20

[2]
Bindin is essential for fertilization in the sea urchin.

Proc Natl Acad Sci U S A. 2021-8-24

[3]
Molecular Mechanisms Influencing Bacterial Conjugation in the Intestinal Microbiota.

Front Microbiol. 2021-6-4

[4]
Oolemma Receptors in Mammalian Molecular Fertilization: Function and New Methods of Study.

Front Cell Dev Biol. 2021-5-19

[5]
Reovirus directly engages integrin to recruit clathrin for entry into host cells.

Nat Commun. 2021-4-12

[6]
Single-cell fluidic force microscopy reveals stress-dependent molecular interactions in yeast mating.

Commun Biol. 2021-1-4

[7]
Single-Virus Force Spectroscopy Discriminates the Intrinsic Role of Two Viral Glycoproteins upon Cell Surface Attachment.

Nano Lett. 2021-1-13

[8]
The Central Role of Cadherins in Gonad Development, Reproduction, and Fertility.

Int J Mol Sci. 2020-11-4

[9]
Force-clamp spectroscopy identifies a catch bond mechanism in a Gram-positive pathogen.

Nat Commun. 2020-10-27

[10]
Molecular mechanisms and evolution of fertilization proteins.

J Exp Zool B Mol Dev Evol. 2021-12

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