TY - JOUR
T1 - Feeling the tension
T2 - the bacterial mechanosensitive channel of large conductance as a model system and drug target
AU - Wang, Junmei
AU - Blount, Paul
N1 - Funding Information:
This research was funded by Grants I-1420 of the Welch Foundation , United States and 1955260 from the National Science Foundation , United States (NSF). The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the paper; or in the decision to publish.
Publisher Copyright:
© 2022 The Author(s)
PY - 2023/2
Y1 - 2023/2
N2 - The drug-resistance crisis has become dire and new antibiotic targets and strategies are required. Mechanosensitive channel of large conductance (MscL) is a conserved bacterial mechanosensitive channel that plays the role of ‘osmotic-emergency-release-valve. It has the largest-gated pore known allowing osmoprotectants out, and other compounds into the cell. Inappropriate gating of the channel can lead to slow growth, decreased viability, and an increase in potency for many antibiotics. The ‘membrane permeability’ observed for some antibiotics, including streptomycin, is mediated by directly binding to and activating MscL. Novel compounds that are MscL agonists have also recently been isolated. Although the compounds are diverse, the binding sites of all characterized MscL-specific agonists are within the same general region of the MscL complex, leading to an in silico screening for compounds that bind this region. In sum, these studies demonstrate that MscL is a viable drug target that may lead to a new generation of antibiotics and adjuvants.
AB - The drug-resistance crisis has become dire and new antibiotic targets and strategies are required. Mechanosensitive channel of large conductance (MscL) is a conserved bacterial mechanosensitive channel that plays the role of ‘osmotic-emergency-release-valve. It has the largest-gated pore known allowing osmoprotectants out, and other compounds into the cell. Inappropriate gating of the channel can lead to slow growth, decreased viability, and an increase in potency for many antibiotics. The ‘membrane permeability’ observed for some antibiotics, including streptomycin, is mediated by directly binding to and activating MscL. Novel compounds that are MscL agonists have also recently been isolated. Although the compounds are diverse, the binding sites of all characterized MscL-specific agonists are within the same general region of the MscL complex, leading to an in silico screening for compounds that bind this region. In sum, these studies demonstrate that MscL is a viable drug target that may lead to a new generation of antibiotics and adjuvants.
UR - http://www.scopus.com/inward/record.url?scp=85147100734&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85147100734&partnerID=8YFLogxK
U2 - 10.1016/j.cophys.2022.100627
DO - 10.1016/j.cophys.2022.100627
M3 - Review article
AN - SCOPUS:85147100734
SN - 2468-8681
VL - 31
JO - Current Opinion in Physiology
JF - Current Opinion in Physiology
M1 - 100627
ER -