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Role of long-range aromatic clique and community in protein stability
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Abstract
Aromatic interactions make an important contribution to protein structure, function, folding and have attracted intense study. Earlier studies on a recombinant xylanase from Bacillus sp. NG-27 (RBSX), which has the ubiquitous (beta/alpha)
8
-triosephosphate isomerase barrel fold showed that three aromatic residues to alanine substitutions, in the N-terminal and C-terminal regions, significantly decreased the stability of the enzyme. Of these mutations, F4A mutation decreased the stability of the enzyme by ∼4 degree C, whereas W6A mutation and Y343A mutation remarkably decreased the stability of the enzyme by ∼10 degree C. On the other hand, the F4W mutation did not affect the thermal stability of RBSX. We provide here a network perspective of aromatic-aromatic interactions in terms of aromatic clique community and long-range association. Our study reveals that disruption of long-range k-clique aromatic interaction cluster holding the N- and C-terminal regions are associated with the decreased stability of the enzyme. The present work reiterates as well as expands on those findings concerning the role of interactions between the N- and C-terminus in protein stability. Furthermore, comparative analyses of crystal structures of homologous pairs of proteins from thermophilic and mesophilic organisms emphasize the prevalence of long-range k-clique communities of aromatic interaction that may be playing an important role and highlights an additional source of stability in thermophilic proteins. The design principle based on clustering of long-range aromatic residues in the form of aromatic-clique and clique community may be effectively applied to enhance the stability of enzymes for biotechnological applications.
Database
The coordinates o fF4A, F4W, W6A, and Y343A are deposited in the PDB database under the accession numbers
5EFF
,
5E58
,
5EFD
, and
5EBA
respectively.
Abbreviations
BSX, xylanase from
Bacilllus sp.
NG-27; RBSX, recombinant BSX xylanase; TIM, Triosephosphate isomerase; GH10, Glycosyl hydrolase family 10; 3D, three-dimensional; r.m.s.d, root mean square deviation; RSA, relative solvent accessible surface area; T
m
, melting temperature; CD, Circular Dichroism; BHX, GH10 xylanase from
Bacillus halodurans
; BFX, GH10 xylanase from
Bacillus firmus
; TmxB, GH10 xylanase from
Thermotoga maritima
Title: Role of long-range aromatic clique and community in protein stability
Description:
Abstract
Aromatic interactions make an important contribution to protein structure, function, folding and have attracted intense study.
Earlier studies on a recombinant xylanase from Bacillus sp.
NG-27 (RBSX), which has the ubiquitous (beta/alpha)
8
-triosephosphate isomerase barrel fold showed that three aromatic residues to alanine substitutions, in the N-terminal and C-terminal regions, significantly decreased the stability of the enzyme.
Of these mutations, F4A mutation decreased the stability of the enzyme by ∼4 degree C, whereas W6A mutation and Y343A mutation remarkably decreased the stability of the enzyme by ∼10 degree C.
On the other hand, the F4W mutation did not affect the thermal stability of RBSX.
We provide here a network perspective of aromatic-aromatic interactions in terms of aromatic clique community and long-range association.
Our study reveals that disruption of long-range k-clique aromatic interaction cluster holding the N- and C-terminal regions are associated with the decreased stability of the enzyme.
The present work reiterates as well as expands on those findings concerning the role of interactions between the N- and C-terminus in protein stability.
Furthermore, comparative analyses of crystal structures of homologous pairs of proteins from thermophilic and mesophilic organisms emphasize the prevalence of long-range k-clique communities of aromatic interaction that may be playing an important role and highlights an additional source of stability in thermophilic proteins.
The design principle based on clustering of long-range aromatic residues in the form of aromatic-clique and clique community may be effectively applied to enhance the stability of enzymes for biotechnological applications.
Database
The coordinates o fF4A, F4W, W6A, and Y343A are deposited in the PDB database under the accession numbers
5EFF
,
5E58
,
5EFD
, and
5EBA
respectively.
Abbreviations
BSX, xylanase from
Bacilllus sp.
NG-27; RBSX, recombinant BSX xylanase; TIM, Triosephosphate isomerase; GH10, Glycosyl hydrolase family 10; 3D, three-dimensional; r.
m.
s.
d, root mean square deviation; RSA, relative solvent accessible surface area; T
m
, melting temperature; CD, Circular Dichroism; BHX, GH10 xylanase from
Bacillus halodurans
; BFX, GH10 xylanase from
Bacillus firmus
; TmxB, GH10 xylanase from
Thermotoga maritima.
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