High concentrations of trimethylamines in slime glands inhibit skein unraveling in Pacific hagfish

Author:

Jain G.1ORCID,Starksen M.1,Singh K.1,Hoang C.1,Yancey P.2,McCord C.13,Fudge D.S.1

Affiliation:

1. Schmid College of Science and Technology, Chapman University, 1 University Dr., Orange, CA 92866, USA

2. Biology Dept., Whitman College, 345 Boyer Ave, Walla Walla, WA 99362, USA

3. Department of Biology, California State University, Dominguez Hills, 1000 E. Victoria Street Carson, CA 90747, USA

Abstract

Hagfish defend themselves from fish predators by producing large volumes of gill-clogging slime when they are attacked. The slime consists of seawater and two major components that are ejected from the slime glands: mucus and threads. The threads are produced within specialized cells and packaged into intricately coiled bundles called skeins. Skeins are kept from unraveling via a protein adhesive that dissolves when the skeins are ejected from the slime glands. Previous work revealed that hagfish slime glands have high concentrations of methylamines including trimethylamine N-oxide (TMAO), betaine (trimethylglycine), and dimethylglycine, however the function of these compounds in the slime glands is unknown. We hypothesized that methylamines have stabilizing effects on the skeins that prevent premature unraveling in the gland. To test this hypothesis, we quantified the effect of methylamines on skein unraveling in Pacific hagfish and found that TMAO and betaine have inhibitory effects on skein unraveling in vitro. Furthermore, we found that TMAO is a more effective inhibitor of unraveling than betaine, but the presence of TMAO synergistically boosts the inhibitory action of betaine. Glycine and dimethyl glycine were far less effective inhibitors of unraveling at natural concentrations. Our results support the hypothesis that high levels of trimethylamines in the slime glands may act to hold the coiled thread skeins together within gland thread cells, and they may do so by stabilizing adhesive proteins. These results advance our knowledge of skein stabilization and deployment and provide another example of trimethylamines functioning to stabilize proteins in a marine organism.

Funder

Kimberly-Clark Corporation

Publisher

The Company of Biologists

Subject

Insect Science,Molecular Biology,Animal Science and Zoology,Aquatic Science,Physiology,Ecology, Evolution, Behavior and Systematics

Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Mechanisms of gill-clogging by hagfish slime;Journal of The Royal Society Interface;2023-03

2. Biological Materials Processing: Time-Tested Tricks for Sustainable Fiber Fabrication;Chemical Reviews;2022-12-12

3. Balancing the Equation: A Natural History of Trimethylamine and Trimethylamine-N-oxide;Journal of Proteome Research;2022-02-10

4. From reductionism to synthesis: The case of hagfish slime;Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology;2021-08

5. A New Model of Hagfish Slime Mucous Vesicle Stabilization and Deployment;Langmuir;2020-05-29

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