Publication:

Structural and Functional Studies of Large-Pore Channels of the CALHM Family

Date

Date

Date
2024
Dissertation

Citations

Citation copied

Drozdzyk, K. (2024). Structural and Functional Studies of Large-Pore Channels of the CALHM Family. (Dissertation, University of Zurich) https://doi.org/10.5167/uzh-258651

Abstract

Abstract

Abstract

A cell relies on proteins, termed ion channels, that facilitate the passage of ions across its membranes. These channels contain pores that activate in response to certain stimuli, allowing ion flow in their open state. Previous research has predominantly focused on ion channels with narrow and selective pores, which permit only certain types of inorganic ions to cross the membrane. However, there is increasing interest in proteins that form channels with wider pores that facilitate the permeation of larger substrates. These large-por

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104 since deposited on 2024-03-20
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Acq. date: 2025-11-12

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192 since deposited on 2024-03-20
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Creators (Authors)

  • Drozdzyk, Katarzyna

Institution

Institution

Institution

Faculty

Faculty

Faculty
Faculty of Science

Item Type

Item Type

Item Type
Dissertation

Referees

  • Dutzler, Raimund
  • Jinek, Martin
  • Albrecht, Christiane

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Language

Language

Language
English

Place of Publication

Place of Publication

Place of Publication
Zürich

Publication date

Publication date

Publication date
2024-03-20

Date available

Date available

Date available
2024-03-20

Number of pages

Number of pages

Number of pages
199

OA Status

OA Status

OA Status
Green

Metrics

Downloads

104 since deposited on 2024-03-20
99last week
Acq. date: 2025-11-12

Views

192 since deposited on 2024-03-20
187last week
Acq. date: 2025-11-12

Citations

Citations

Citation copied

Drozdzyk, K. (2024). Structural and Functional Studies of Large-Pore Channels of the CALHM Family. (Dissertation, University of Zurich) https://doi.org/10.5167/uzh-258651

Green Open Access
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