A skewed distribution of amino acids at recognition sites of the hypervariable region of immunoglobulins

1994 ◽  
Vol 38 (1) ◽  
Author(s):  
E. Vargas-Madrazo ◽  
F. Lara-Ochoa ◽  
M. Jim�nez-Monta�o
2000 ◽  
Vol 81 (12) ◽  
pp. 2873-2883 ◽  
Author(s):  
Arvind H. Patel ◽  
Jonny Wood ◽  
Francois Penin ◽  
Jean Dubuisson ◽  
J. A. McKeating

We compared the ability of two closely related truncated E2 glycoproteins (E2660) derived from hepatitis C virus (HCV) genotype 1a strains Glasgow (Gla) and H77c to bind a panel of conformation-dependent monoclonal antibodies (MAbs) and CD81. In contrast to H77c, Gla E2660 formed disulfide-linked high molecular mass aggregates and failed to react with conformation-dependent MAbs and CD81. To delineate amino acid (aa) regions associated with protein aggregation and CD81 binding, several Gla–H77c E2660 chimeric glycoproteins were constructed. Chimeras C1, C2 and C6, carrying aa 525–660 of Gla E2660, produced disulfide-linked aggregates and failed to bind CD81 and conformation-dependent MAbs, suggesting that amino acids within this region are responsible for protein misfolding. The presence of Gla hypervariable region 1 (aa 384–406) on H77 E2660, chimera C4, had no effect on protein folding or CD81 binding. Chimeras C3 and C5, carrying aa 384–524 or 407–524 of Gla E2660, respectively, were recognized by conformation-dependent MAbs and yet failed to bind CD81, suggesting that amino acids in region 407–524 are important in modulating CD81 interaction without affecting antigen folding. Comparison of Gla and H77c E2660 aa sequences with those of genotype 1a and divergent genotypes identified a number of variant amino acids, including two putative N-linked glycosylation sites at positions 476 and 532. However, introduction of G476N–G478S and/or D532N in Gla E2660 had no effect on antigenicity or aggregation.


Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2232 ◽  
Author(s):  
Jiahui Wang ◽  
Hao Zhang ◽  
Ruifang Guan

Dual-emission nanosensor for Hg2+ detection was prepared by coupling CA-AEAPMS on the surface of RBS-doped modified silica microspheres. The CA-AEAPMS was synthesized by using N-(β-aminoethyl)-γ-aminopropyl methyldimethoxysilane (AEAPMS) and citric acid as the main raw material. The obtained nanosensor showed characteristic fluorescence emissions of Rhodamine B (red) and CA-AEAPMS (blue) under a single excitation wavelength (360 nm). Upon binding to Hg2+, only the fluorescence of CA-AEAPMS was quenched, resulting in the ratiometric fluorescence response of the dual-emission silica microspheres. This ratiometric nanosensor exhibited good selectivity to Hg2+ over other metal ions, because of the amide groups on the surface of CA-AEAPMS serving as the Hg2+ recognition sites. The ratio of F450/F580 linearly decreased with the increasing of Hg2+ concentration in the range of 0 to 3 × 10−6 M, and a detection limit was as low as 97 nM was achieved. Then, the addition of three thiol-containing amino acids (Cys, Hcy, GSH) to the quenched fluorescence solution with Hg2+ can restore the fluorescence, and the detection limits of the three biothiols (Cys, Hcy, GSH) are 0.133 μM, 0.086 μM, and 0.123 μM, respectively.


1981 ◽  
Author(s):  
D W Chung ◽  
M W Rixon ◽  
R T A MacGillivray ◽  
E W Davie

Radioactive cDNA was synthesized from a bovine liver mRNA preparation enriched for fibrinogen mRNA activity. This cDNA was used in a solution hybridization assay to screen a collection of recombinant plasmids carrying bovine cDNA inserts. A number of plasmids containing cDNAs for fibrinogen were identified.The nucleotide sequence of the insert of one plasmid, designated pBIβ1, has been determined. It contains 1372 base pairs and codes for the C-terminal 424 amino acids of the β chain of bovine fibrinogen. This and other previous-ly reported partial sequences enabled the construction of the complete amino acid sequence of the bovine β chain. Comparison of this sequence with that of the human β chain shows a high degree of homology. The positions of all the cystine and tryptophan residues are identical.The nucleotide sequence of the insert of another plasmid, designated pBIα1, has also been determined. This plasmid contains 965 base pairs and codes for the C-terminal 203 amino acids of the bovine a chain. This region shows only 46% homology with the corresponding region in the human α chain. A hypervariable region, consisting of 53 amino acids, is present in the bovine a chain. This region shows little homology with the corresponding region in the human α chain. Furthermore, it is 26 amino acids shorter than the corresponding region in the human a chain.The cDNAs to the bovine fibrinogen chains will provide good probes for the study of human fibrinogen and the organization and structure of its genomic DNA.


1998 ◽  
Vol 365 (1-3) ◽  
pp. 59-67 ◽  
Author(s):  
Masakazu Yoshikawa ◽  
Takashi Fujisawa ◽  
Jun-ichiro Izumi ◽  
Toshio Kitao ◽  
Shunji Sakamoto

1993 ◽  
Vol 177 (1) ◽  
pp. 119-125 ◽  
Author(s):  
J White ◽  
A Pullen ◽  
K Choi ◽  
P Marrack ◽  
J W Kappler

We examined the effect of mutations in the V beta portion of a pigeon cytochrome c (cyto c)-specific V beta 3+/V alpha 11+ T cell receptor on its ability to recognize cyto c/IEk and various superantigens. The results were consistent with an immunoglobulin-like structure for the receptor V beta domain and with separate interaction sites on V beta for conventional antigen and superantigens. An amino acid predicted to lie in CDR1 was critical for cyto c/IEk but not superantigen recognition, while several amino acids predicted to lie in the hypervariable region 4 loop were critical for superantigen but not cyto c/IEk recognition.


2020 ◽  
Vol 8 (11) ◽  
pp. 1630
Author(s):  
Berenice Palacios-González ◽  
Eric G. Ramírez-Salazar ◽  
Berenice Rivera-Paredez ◽  
Manuel Quiterio ◽  
Yvonne N. Flores ◽  
...  

The effect of microbiota composition and its health on bone tissue is a novel field for research. However, their associations with bone mineral density (BMD) have not been established in postmenopausal women. The present study investigates the relation of diet, the microbiota composition, and the serum metabolic profile in postmenopausal women with normal-BMD or with low-BMD. Ninety-two Mexican postmenopausal women were classified into normal-BMD (n = 34) and low-BMD (n = 58). The V4 hypervariable region was sequenced using the Miseq platform. Serum vitamin D was determined by chemiluminescence immunoassay. Serum concentrations of acyl-carnitines and amino acids were determined by electrospray tandem mass spectrometry. Diet was assessed by a food frequency questionnaire. The low-BMD group had fewer observed species, higher abundance of γ-Proteobacteria, lower consumption of lycopene, and lower concentrations of leucine, valine, and tyrosine compared with the normal-BMD group. These amino acids correlated positively with the abundance of Bacteroides. Lycopene consumption positively correlated with Oscillospira and negatively correlated with Pantoea genus abundance. Finally, the intestinal microbiota of women with vitamin D deficiency was related to Erysipelotrichaceae and Veillonellaceae abundance compared to the vitamin D non-deficient group. Associations mediated by the gut microbiota between diet and circulating metabolites with low-BMD were identified.


2021 ◽  
Vol 12 ◽  
Author(s):  
Amy Atter ◽  
Maria Diaz ◽  
Kwaku Tano-Debrah ◽  
Angela Parry-Hanson Kunadu ◽  
Melinda J. Mayer ◽  
...  

Hausa koko is an indigenous porridge processed from millet in Ghana. The process involves fermentation stages, giving the characteristic organoleptic properties of the product that is produced largely at a small-scale household level and sold as a street food. Like many other indigenous foods, quality control is problematic and depends on the skills of the processor. In order to improve the quality of the product and standardize the process for large-scale production, we need a deeper understanding of the microbial processes. The aim of this study is to investigate the microbial community involved in the production of this traditional millet porridge and the metabolites produced during processing. High-throughput amplicon sequencing was used to identify the bacterial (16S rRNA V4 hypervariable region) and fungal [Intergenic Transcribed Spacer (ITS)] communities associated with the fermentation, while nuclear magnetic resonance (NMR) was used for metabolite profiling. The bacterial community diversity was reduced during the fermentation processes with an increase and predominance of lactobacilli. Other dominant bacteria in the fermentation included Pediococcus, Weissella, Lactococcus, Streptococcus, Leuconostoc, and Acetobacter. The species Limosilactobacillus fermentum and Ligilactobacillus salivarius accounted for some of the diversities within and between fermentation time points and processors. The fungal community was dominated by the genus Saccharomyces. Other genera such as Pichia, Candida, Kluyveromyces, Nakaseomyces, Torulaspora, and Cyberlindnera were also classified. The species Saccharomyces cerevisiae, Stachybotrys sansevieriae, Malassezia restricta, Cyberlindnera fabianii, and Kluyveromyces marxianus accounted for some of the diversities within some fermentation time points. The species S. sansevieria and M. restricta may have been reported for the first time in cereal fermentation. This is the most diverse microbial community reported in Hausa koko. In this study, we could identify and quantify 33 key different metabolites produced by the interactions of the microbial communities with the millet, composed of organic compounds, sugars, amino acids and intermediary compounds, and other key fermentation compounds. An increase in the concentration of organic acids in parallel with the reduction of sugars occurred during the fermentation process while an initial increase of amino acids followed by a decrease in later fermentation steps was observed.


1976 ◽  
Vol 157 (2) ◽  
pp. 449-459 ◽  
Author(s):  
J C Jaton

The amino acid sequence of the V (variable) region of the heavy (H) chain of rabbit antibody BS-1, raised against type III pneumococcal vaccine, is reported. Together with the sequence data of the V region of the light (L) chain previously determined [Jaton (1974a) Biochem. J. 141, 1-13], the present work completes the analysis of the V domain of the homogeneous antibody BS-1. The V domains (VL + VH regions) of this antibody are compared with those of two other anti-(type III) pneumococcal antibodies BS-5 and K-25 [Jaton (1975) Biochem. J. 147, 235-247]. Except for the second hypervariable section of the L chains, these antibodies have very different sequences in the hypervariable segments of the V domains. Within the third hypervariable region of the H chain, each antibody has a different length: BS-1 is three amino acids shorter than K-25 and two amino acids shorter than BS-5. When the sequences in that section are aligned for maximal homology, only two residues, glycine-97 and leucine-101, are common to the three antibodies. On the basis of the amino acid sequences of these three anti-pneumococcal antibodies, the results do not support the concept of a simple correlation between primary structure in the hypervariable sections (known to determine the shape of the combining site) and antigen-binding specificity.


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