Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

In this hybrid review, we have first collected and reviewed available information on the structure and function of the enigmatic cache domains in αδ proteins. These are organized into two double cache (dCache_1) domains, and they are present in all αδ proteins. We have also included new data on the key function of these domains with respect to amino acid and gabapentinoid binding to the universal amino acid-binding pocket, which is present in αδ-1 and αδ-2. We have now identified the reason why αδ-3 and αδ-4 do not bind gabapentinoid drugs or amino acids with bulky side chains. In relation to this, we have determined that the bulky amino acids Tryptophan and Phenylalanine prevent gabapentin from inhibiting cell surface trafficking of αδ-1. Together, these novel data shed further light on the importance of the cache domains in αδ proteins.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901441PMC
http://dx.doi.org/10.1080/19336950.2023.2167563DOI Listing

Publication Analysis

Top Keywords

domains αδ
16
αδ proteins
16
cache domains
12
amino acids
8
cache
4
αδ
4
proteins
4
proteins basis
4
basis gabapentinoid
4
gabapentinoid selectivity
4

Similar Publications

AaaA is a virulence-associated outer membrane protein found in the Gram-negative pathogen Pseudomonas aeruginosa. Classified as both an autotransporter and a member of the M28 family of aminopeptidases, AaaA has been shown to cleave N-terminal arginine residues from host-derived peptides. This activity has been demonstrated to enhance bacterial survival and suppress host immune responses by increasing local arginine availability.

View Article and Find Full Text PDF

The protein therapeutics market, including antibody and fusion proteins, has experienced steady growth over the past decade, underscoring the importance of optimizing amino acid sequences. In our previous study, we developed a fusion protein, R31, which combines retinol-binding protein (RBP) with albumin domains IIIA and IB, linked by a sequence (AAAA), and includes an additional disulfide bond (N227C-V254C) in IIIA. This fusion protein effectively inhibited hepatic stellate cell activation.

View Article and Find Full Text PDF

The significant growth of the global protein drug market, including fusion proteins, emphasizes the crucial role of optimizing amino acid sequences to enhance the productivity and bioefficacy. Among these fusion proteins, RBP-IIIA-IB, comprising retinol-binding protein in conjunction with the albumin domains, IIIA and IB, has displayed efficacy in alleviating liver fibrosis by inhibiting the activation of hepatic stellate cells (HSCs). This study aimed to address the issue of the low productivity in RBP-IIIA-IB.

View Article and Find Full Text PDF

The sodium (Na) leak channel (NALCN) is a member of the four-domain voltage-gated cation channel family that includes the prototypical voltage-gated sodium and calcium channels (Nas and Cas, respectively). Unlike Nas and Cas, which have four lateral fenestrations that serve as routes for lipophilic compounds to enter the central cavity to modulate channel function, NALCN has bulky residues (W311, L588, M1145, and Y1436) that block these openings. Structural data suggest that occluded fenestrations underlie the pharmacological resistance of NALCN, but functional evidence is lacking.

View Article and Find Full Text PDF
Article Synopsis
  • The sodium leak channel (NALCN) is distinct from traditional voltage-gated channels like Na and Ca channels, having blocked openings that prevent lipophilic compounds from modulating its function.
  • Experiments showed that changing specific amino acids in NALCN allowed researchers to study how certain blockers, like phenytoin and 2-APB, interact differently with the channel, revealing unique pathways for drug access.
  • These findings enhance our understanding for future drug design aimed at targeting NALCN specifically, despite its overall resistance to pharmacological manipulation.
View Article and Find Full Text PDF